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      • petersfield, south east
      • permanent
      • randstad cpe
      I have an exciting opportunity for an experienced EHS Capital Project Manager within the Global Environmental Affairs & Safety department to join a leading laboratory business on a permanent basis. As EHS Project Manager, you will:Develop capital project documentation through to execution and completion of various safety, environmental and sustainability projects to help reach ESG goals.Manage individual capital projects following best practices and techniques from conception, design, procurement, installation, commissioning, and final handover.Application of GMP/OTC or other quality protocols or requirements may need to be met. Manage numerous projects (from small to large) in tandem and ensure that internal and external resources are aligned, and projects completed in priority order. To be considered for the role of EHS Project Manager, you will:Coaching, influencing, team building with colleagues that are not direct reports or within EHS organisationAdvanced project management skills with attention to detailGood negotiation skills such as tendering process with external suppliers matched up with a solid understanding of cost implicationsFluent in suite of Microsoft applications, reporting tools (CR360) and Experience with QuickBase is a plusManaging projects from concept, delivery, to completion. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      I have an exciting opportunity for an experienced EHS Capital Project Manager within the Global Environmental Affairs & Safety department to join a leading laboratory business on a permanent basis. As EHS Project Manager, you will:Develop capital project documentation through to execution and completion of various safety, environmental and sustainability projects to help reach ESG goals.Manage individual capital projects following best practices and techniques from conception, design, procurement, installation, commissioning, and final handover.Application of GMP/OTC or other quality protocols or requirements may need to be met. Manage numerous projects (from small to large) in tandem and ensure that internal and external resources are aligned, and projects completed in priority order. To be considered for the role of EHS Project Manager, you will:Coaching, influencing, team building with colleagues that are not direct reports or within EHS organisationAdvanced project management skills with attention to detailGood negotiation skills such as tendering process with external suppliers matched up with a solid understanding of cost implicationsFluent in suite of Microsoft applications, reporting tools (CR360) and Experience with QuickBase is a plusManaging projects from concept, delivery, to completion. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • queenborough, south east
      • permanent
      • £32,000 - £37,000, per year, Depending on experience
      • randstad cpe
      Are you an experienced Quality Control Analyst? Are you looking for your next position in an exciting Pharma development company?My client, a leading Pharma development business has an exciting opportunity for a Senior QC Analyst to join their team in Kent. As Senior QC Analyst, you will:Testing raw materials, in-process, finished product and stability samplesEnsure that the production schedules are met.Liaise with production management, quality, planning and technical to ensure that the needs of customers are identified and satisfied to high standardsEnsure all activities are performed in compliance with customer and ICH procedures To be considered for the role of Senior QC Analyst, you'll:Educated to degree level in a scientific field Significant experience in a pharmaceutical laboratory environment and cGMP requirementsProven experience/ skill with HPLC, GV, UV, FTIR and DissolutionRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you an experienced Quality Control Analyst? Are you looking for your next position in an exciting Pharma development company?My client, a leading Pharma development business has an exciting opportunity for a Senior QC Analyst to join their team in Kent. As Senior QC Analyst, you will:Testing raw materials, in-process, finished product and stability samplesEnsure that the production schedules are met.Liaise with production management, quality, planning and technical to ensure that the needs of customers are identified and satisfied to high standardsEnsure all activities are performed in compliance with customer and ICH procedures To be considered for the role of Senior QC Analyst, you'll:Educated to degree level in a scientific field Significant experience in a pharmaceutical laboratory environment and cGMP requirementsProven experience/ skill with HPLC, GV, UV, FTIR and DissolutionRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • wicklow, international
      • permanent
      • randstad financial services
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Responsibilities:Ensures manufacturing operations are continually supported and maintained in compliance with all quality, safety and environmental regulations.Technical transfer, Scale-up & Installation of new processes & new unit operations onto and with-in the plant.Support Process & Facility start-ups, initial campaigns & process optimisation.Complete detailed Equipment and Process assessments.Project Management of wide scope cross functional projects.Application of Six Sigma and Lean methodologies when undertaking projects and coaching others in use of these tools as part of their application.Ensure campaign preparations for individual processes are achieved to facilitate on‐time campaign start‐up and adherence of agreed production rate.Takes ownership for assigned process steps and provide process technical support as required.Lead cross functional investigations within operations. Use lean six sigma tools to drive root cause analysis and CAPA completion.The preparation and routine review of Batch Records, Cleaning Procedures, Equipment Operating Procedures, Standard Operating Procedures, Protocols and Summary Reports. These updates include actively making changes to drive improvements, increase in RFT and decrease in deviations.The development and update of control system recipes.Participation in audits, quality monitoring inspections and self-inspections as required. Lead cycle time reduction initiatives.Participation and driving of Continuous Improvement Activities.Lead EHS activities including Process HAZOP.Preparation of change control packages.Skills and Experience:3 to 5 years of experience in a technical role in the Pharmaceutical industry.Degree in Chemical/Process Engineering or Chemistry.Technical skills and competencies:Strong leadership, communication, decision making and problem solving skills.Experience with 6 sigma or other operational excellence tools.Experience of working in a cross functional team in a highly regulated environment.Experience of technology transfer and a new product/equipment start-up.An understanding of computer control systems, P.I.D loops and interlock devices.Ability to manage multiple projects simultaneously and prioritise work, goals and tasks in accordance with division and corporate objectives.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Responsibilities:Ensures manufacturing operations are continually supported and maintained in compliance with all quality, safety and environmental regulations.Technical transfer, Scale-up & Installation of new processes & new unit operations onto and with-in the plant.Support Process & Facility start-ups, initial campaigns & process optimisation.Complete detailed Equipment and Process assessments.Project Management of wide scope cross functional projects.Application of Six Sigma and Lean methodologies when undertaking projects and coaching others in use of these tools as part of their application.Ensure campaign preparations for individual processes are achieved to facilitate on‐time campaign start‐up and adherence of agreed production rate.Takes ownership for assigned process steps and provide process technical support as required.Lead cross functional investigations within operations. Use lean six sigma tools to drive root cause analysis and CAPA completion.The preparation and routine review of Batch Records, Cleaning Procedures, Equipment Operating Procedures, Standard Operating Procedures, Protocols and Summary Reports. These updates include actively making changes to drive improvements, increase in RFT and decrease in deviations.The development and update of control system recipes.Participation in audits, quality monitoring inspections and self-inspections as required. Lead cycle time reduction initiatives.Participation and driving of Continuous Improvement Activities.Lead EHS activities including Process HAZOP.Preparation of change control packages.Skills and Experience:3 to 5 years of experience in a technical role in the Pharmaceutical industry.Degree in Chemical/Process Engineering or Chemistry.Technical skills and competencies:Strong leadership, communication, decision making and problem solving skills.Experience with 6 sigma or other operational excellence tools.Experience of working in a cross functional team in a highly regulated environment.Experience of technology transfer and a new product/equipment start-up.An understanding of computer control systems, P.I.D loops and interlock devices.Ability to manage multiple projects simultaneously and prioritise work, goals and tasks in accordance with division and corporate objectives.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      • wicklow, international
      • permanent
      • randstad financial services
      Chemical Engineer Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Responsibilities Support process & facility start-up initiatives.Support HAZOP/ process risk assessments plan.Support the engineering department in the application of Process Safety elements. Assist with technology transfer of API processes, including process fit, identification of equipment needs, and facility modifications.Provide oversight for Mechanical Integrity Programs (I&E, Fire Protection, Equipment, RVs, Piping, etc.)Collaborate closely with Operations colleagues in the preparation of Master Batch Records and execution of process HAZOPs, Hazard identification, risk assessments and chemical agent risk assessments and FMEAs for tech transfer of API processes.Supporting improvement of chemical manufacturing process safety performance, product transfers and new product introductions.Assist in the design and implementation of reliable and cost-effective engineering solutionsFacilitate the management of change processes from a process safety perspective.Collect and analyze technical data, generate reports including conclusions and recommendations where needed.Manage close out actions for production/projects etc. RequirementsAn honours degree in Chemical Engineering or related discipline.Minimum 2 year's experience in Pharmaceutical Manufacturing.Experience working in an API environment, desirable.Knowledge of mechanical systems (HVAC systems, power generation, utilities)Ability to read engineering drawings.Mastery of chemical engineering principles, practices and theories with pharmaceutical experience.Experience with scale-up techniques for processes from laboratory to plant scale.Due to a high volume of applications only those progressing to the next stage will be contacted.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      Chemical Engineer Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Responsibilities Support process & facility start-up initiatives.Support HAZOP/ process risk assessments plan.Support the engineering department in the application of Process Safety elements. Assist with technology transfer of API processes, including process fit, identification of equipment needs, and facility modifications.Provide oversight for Mechanical Integrity Programs (I&E, Fire Protection, Equipment, RVs, Piping, etc.)Collaborate closely with Operations colleagues in the preparation of Master Batch Records and execution of process HAZOPs, Hazard identification, risk assessments and chemical agent risk assessments and FMEAs for tech transfer of API processes.Supporting improvement of chemical manufacturing process safety performance, product transfers and new product introductions.Assist in the design and implementation of reliable and cost-effective engineering solutionsFacilitate the management of change processes from a process safety perspective.Collect and analyze technical data, generate reports including conclusions and recommendations where needed.Manage close out actions for production/projects etc. RequirementsAn honours degree in Chemical Engineering or related discipline.Minimum 2 year's experience in Pharmaceutical Manufacturing.Experience working in an API environment, desirable.Knowledge of mechanical systems (HVAC systems, power generation, utilities)Ability to read engineering drawings.Mastery of chemical engineering principles, practices and theories with pharmaceutical experience.Experience with scale-up techniques for processes from laboratory to plant scale.Due to a high volume of applications only those progressing to the next stage will be contacted.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      • wicklow, international
      • permanent
      • randstad financial services
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries.Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D.Benefits: Competitive salary and bonus. Pension contribution. Private Health Insurance. Life Assurance.Shared Ownership schemes. Responsibilities: Support the development of a Central Engineering Database and Centre of Excellence for API process plant.Engineering oversight of process plant equipment. Support the scoping and early Engineering design of new process introductions and process improvement projects.Scope, develop and lead new projects related to process plant equipment improvements. Ensure that process plant equipment is maintained in accordance with vendor & legislative requirements.Support the Safety Controls & Interlock strategy for the site.Support the development of the site strategy for process plant equipment risk assessments and compliance with Machinery Directive guidelines.Ensure our client and regulatory agency policies and standards for plant equipment are fully complied with including Quality, EHS, FDA, HPRA, EPA, HSA.Interface with regulatory agencies during site audits and walk downs.Work closely with EHS, Operations, Utilities, Automation and Maintenance personnel to ensure equipment is safe to operate & maintain.Education and Experience: Bachelor's Degree in Mechanical, Chemical, Process or Electrical Engineering, honours grade.3 years plus experience in GMP manufacturing environment.Understanding of GMP and Quality standards.Experience of the Operation and Maintenance of Manufacturing process systems within a regulated environment.Familiarity with Machinery Directive legislation & implementation within an ATEX environment would be an advantage. Due to a high volume of applicants only those progressing to the next stage will be contacted. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries.Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D.Benefits: Competitive salary and bonus. Pension contribution. Private Health Insurance. Life Assurance.Shared Ownership schemes. Responsibilities: Support the development of a Central Engineering Database and Centre of Excellence for API process plant.Engineering oversight of process plant equipment. Support the scoping and early Engineering design of new process introductions and process improvement projects.Scope, develop and lead new projects related to process plant equipment improvements. Ensure that process plant equipment is maintained in accordance with vendor & legislative requirements.Support the Safety Controls & Interlock strategy for the site.Support the development of the site strategy for process plant equipment risk assessments and compliance with Machinery Directive guidelines.Ensure our client and regulatory agency policies and standards for plant equipment are fully complied with including Quality, EHS, FDA, HPRA, EPA, HSA.Interface with regulatory agencies during site audits and walk downs.Work closely with EHS, Operations, Utilities, Automation and Maintenance personnel to ensure equipment is safe to operate & maintain.Education and Experience: Bachelor's Degree in Mechanical, Chemical, Process or Electrical Engineering, honours grade.3 years plus experience in GMP manufacturing environment.Understanding of GMP and Quality standards.Experience of the Operation and Maintenance of Manufacturing process systems within a regulated environment.Familiarity with Machinery Directive legislation & implementation within an ATEX environment would be an advantage. Due to a high volume of applicants only those progressing to the next stage will be contacted. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Chemistry Research Associate? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! We're looking for a materials chemist who specialise in technology and biomaterial development to meet our clients goals. This is a lab-based role and your work will centre on optimising biomaterial performance. Training will be provided for all aspects but hands-on experience in chemical synthesis is expected and knowledge/experience in polymers is desirable.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Synthesise biomaterials for production, novel biomaterials for testing and evaluation.Characterise chemical and material properties.Assist team members with biological assays.Scale reactions from lab to pilot scale (g to kg).Assist in the generation of SOPs, COSHH and risk assessments.Participate in R&D meetings, sharing skills and expertise with team members.Maintain equipment and order reagents/solvents.Ensure accurate recording of experiments using electronic laboratory notebook.Qualifications: Degree in Chemistry or related discipline with practical experience in chemical synthesis.Essential Experience:Formulating and processing natural polymers (e.g. polysaccharides, proteins, lipids), hydrogels and/or protein/enzyme solutions.Chemical/mechanical characterisation of materials (e.g. GPC/SEC-HPLC, NMR, FTIR, TGA/DSC, tensile testing).Laboratory experience - previously conducted research project with chemical synthesis and characterisation with an understanding of chemical hazards and safety protocols.Good knowledge of standard chemical methods in purification, isolation and work-up of small molecules (solvents, monomers etc).Desirable experience: Practical experience in polymer synthesis (e.g. RAFT, ATRP, ring-opening or anionic), processes (e.g. bulk, emulsion, solution), post-polymerisation modification or hydrogel processing methodologies.Experience working with biomaterials or academic understanding of cell-material interfaces.Prior experience with working in a clean room, biological safety cabinet or aseptic handling/sterilisation methods.Experience communicating across disciplines or in multi-disciplinary teams.Experience with factorial design of experiments.Basic understanding of patents and IP.Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Chemistry Research Associate? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! We're looking for a materials chemist who specialise in technology and biomaterial development to meet our clients goals. This is a lab-based role and your work will centre on optimising biomaterial performance. Training will be provided for all aspects but hands-on experience in chemical synthesis is expected and knowledge/experience in polymers is desirable.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Synthesise biomaterials for production, novel biomaterials for testing and evaluation.Characterise chemical and material properties.Assist team members with biological assays.Scale reactions from lab to pilot scale (g to kg).Assist in the generation of SOPs, COSHH and risk assessments.Participate in R&D meetings, sharing skills and expertise with team members.Maintain equipment and order reagents/solvents.Ensure accurate recording of experiments using electronic laboratory notebook.Qualifications: Degree in Chemistry or related discipline with practical experience in chemical synthesis.Essential Experience:Formulating and processing natural polymers (e.g. polysaccharides, proteins, lipids), hydrogels and/or protein/enzyme solutions.Chemical/mechanical characterisation of materials (e.g. GPC/SEC-HPLC, NMR, FTIR, TGA/DSC, tensile testing).Laboratory experience - previously conducted research project with chemical synthesis and characterisation with an understanding of chemical hazards and safety protocols.Good knowledge of standard chemical methods in purification, isolation and work-up of small molecules (solvents, monomers etc).Desirable experience: Practical experience in polymer synthesis (e.g. RAFT, ATRP, ring-opening or anionic), processes (e.g. bulk, emulsion, solution), post-polymerisation modification or hydrogel processing methodologies.Experience working with biomaterials or academic understanding of cell-material interfaces.Prior experience with working in a clean room, biological safety cabinet or aseptic handling/sterilisation methods.Experience communicating across disciplines or in multi-disciplinary teams.Experience with factorial design of experiments.Basic understanding of patents and IP.Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Senior Scientist? Are you looking for a Team Leader role? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Senior Scientist to work as our clients Culture Medium Team Leader. Your primary focus is to develop culture medium formulations using high-throughput technology towards animal component free, low cost, large-scale and reproducible manufacture of cultivated meat. You will work closely with the other R&D teams to optimise protocols and deliver our company-wide milestones.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Design, plan, and perform R&D Culture Medium activities, ensuring that deliverables are successfully met within project timelinesLead and develop the Culture Medium team to deliver on R&D milestonesProvide guidance and coaching to support the growth of the Culture medium teamDetermine the most appropriate methodologies to test hypotheses, and identify suitable alternatives if technical problems ariseGather, analyse, and present scientific data from a variety of sourcesDocument research findings clearly in an electronic lab bookSelect, follow, and further develop experimental protocols and generate laboratory SOPsProvide general laboratory management and administrationSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsParticipate as a key member of the R&D management team with responsibility for day-to-day decision making within your teamProvide written and verbal progress reports to the Senior Leadership Team and to external collaboratorsContribute to discussions and share research findings with colleagues in partner institutions, and research groups (as required)Keep up to date with field developments and apply these to improve experimental design and assay performanceQualifications: A PhD in a relevant area of Biological Sciences or related field≥ 6 years of post-doctoral or industry experience in relevant areaEssential experience required: In-depth experience in cell culture: isolation, maintenance and differentiation of stem or primary cell typesExpertise in cellular and molecular biology assays such as enzyme-based metabolism assays, protein quantification, ICH & PCRProven experience in the development of cell-based processes, including in-depth expertise in cultured cell biochemistry, metabolism and culture medium developmentSkilled at the design, set up and running of complex experimentsProficient in the detailed analysis and presentation of complex data setsMathematically literateFamiliarity with the development and implementation of automation to support high-throughput media developmentExperience of writing SOPs and risk assessments under quality management systemHighly organised, self-motivated, and capable of working both independently and collaboratively, in a fast-paced team environment with shifting prioritiesRoot cause analysis and problem solvingManagement experience with a proven track record of success delivering R&D projectsA proven history of independent investigations and innovative thinkingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Senior Scientist? Are you looking for a Team Leader role? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Senior Scientist to work as our clients Culture Medium Team Leader. Your primary focus is to develop culture medium formulations using high-throughput technology towards animal component free, low cost, large-scale and reproducible manufacture of cultivated meat. You will work closely with the other R&D teams to optimise protocols and deliver our company-wide milestones.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Design, plan, and perform R&D Culture Medium activities, ensuring that deliverables are successfully met within project timelinesLead and develop the Culture Medium team to deliver on R&D milestonesProvide guidance and coaching to support the growth of the Culture medium teamDetermine the most appropriate methodologies to test hypotheses, and identify suitable alternatives if technical problems ariseGather, analyse, and present scientific data from a variety of sourcesDocument research findings clearly in an electronic lab bookSelect, follow, and further develop experimental protocols and generate laboratory SOPsProvide general laboratory management and administrationSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsParticipate as a key member of the R&D management team with responsibility for day-to-day decision making within your teamProvide written and verbal progress reports to the Senior Leadership Team and to external collaboratorsContribute to discussions and share research findings with colleagues in partner institutions, and research groups (as required)Keep up to date with field developments and apply these to improve experimental design and assay performanceQualifications: A PhD in a relevant area of Biological Sciences or related field≥ 6 years of post-doctoral or industry experience in relevant areaEssential experience required: In-depth experience in cell culture: isolation, maintenance and differentiation of stem or primary cell typesExpertise in cellular and molecular biology assays such as enzyme-based metabolism assays, protein quantification, ICH & PCRProven experience in the development of cell-based processes, including in-depth expertise in cultured cell biochemistry, metabolism and culture medium developmentSkilled at the design, set up and running of complex experimentsProficient in the detailed analysis and presentation of complex data setsMathematically literateFamiliarity with the development and implementation of automation to support high-throughput media developmentExperience of writing SOPs and risk assessments under quality management systemHighly organised, self-motivated, and capable of working both independently and collaboratively, in a fast-paced team environment with shifting prioritiesRoot cause analysis and problem solvingManagement experience with a proven track record of success delivering R&D projectsA proven history of independent investigations and innovative thinkingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Scientist? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! As a scientist you will join our client's Cell Biology Team! The purpose of this role is to conduct scientific work, to support the development and production of animal myoblasts or adipocytes from stem cells to replace muscle or fat grown in animals. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Develop, optimise and characterise stem cell cultures and differentiation protocols to maximise conversion into muscle or fat cellsOptimise protocols for isolation and maintenance of primary stem cells in vitroDesign, plan, and execute complex R&D experiments ensuring that deliverables are successfully met within timelinesDocument research findings clearly in a lab bookCommunicate regularly in group meetings and prepare and deliver presentations to project team and internal stakeholdersAlong with team members, provide routine laboratory maintenance, including participating in equipment upkeep, cleaning rotas and laboratory consumables stock managementShared responsibility for out-of-hours cell culture maintenanceEnsure that laboratory health, safety and quality procedures are followedSelect, follow, and adapt experimental protocols and generate laboratory SOPsSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsMaintain the confidentiality of the project and protocolsKeep abreast of current technologies and relevant scientific literature to help identify opportunity for improvements and reduction of costs Qualifications: Master or PhD in Life Sciences, Biotechnology or related fieldTwo or more years of postdoctoral experience or industry experience in myogenesis or adipogenesis Essential Experience: Extensive experience in muscle or fat biology, with deep knowledge in stem cell biology, cell metabolism and developmentProven experience in cell culture, including maintenance and differentiation of stem cellsSubstantial experience in molecular biology techniques such as PCR, qRT-PCR, Western Blot, Flow cytometry and ImagingAbility to work independently and as part of growing teamSkilled in troubleshooting and conducting multi-factorial experimentsGood numeracy, computer and communication skills Desirable Experience: Experience with cell isolation protocols from biological samplesFamiliarity with co-cultures and 3D culture systemsApplication of Design of Experiments (DoE) to rationalize experiment designExperience of writing SOPs and risk assessmentsRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Scientist? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! As a scientist you will join our client's Cell Biology Team! The purpose of this role is to conduct scientific work, to support the development and production of animal myoblasts or adipocytes from stem cells to replace muscle or fat grown in animals. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Develop, optimise and characterise stem cell cultures and differentiation protocols to maximise conversion into muscle or fat cellsOptimise protocols for isolation and maintenance of primary stem cells in vitroDesign, plan, and execute complex R&D experiments ensuring that deliverables are successfully met within timelinesDocument research findings clearly in a lab bookCommunicate regularly in group meetings and prepare and deliver presentations to project team and internal stakeholdersAlong with team members, provide routine laboratory maintenance, including participating in equipment upkeep, cleaning rotas and laboratory consumables stock managementShared responsibility for out-of-hours cell culture maintenanceEnsure that laboratory health, safety and quality procedures are followedSelect, follow, and adapt experimental protocols and generate laboratory SOPsSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsMaintain the confidentiality of the project and protocolsKeep abreast of current technologies and relevant scientific literature to help identify opportunity for improvements and reduction of costs Qualifications: Master or PhD in Life Sciences, Biotechnology or related fieldTwo or more years of postdoctoral experience or industry experience in myogenesis or adipogenesis Essential Experience: Extensive experience in muscle or fat biology, with deep knowledge in stem cell biology, cell metabolism and developmentProven experience in cell culture, including maintenance and differentiation of stem cellsSubstantial experience in molecular biology techniques such as PCR, qRT-PCR, Western Blot, Flow cytometry and ImagingAbility to work independently and as part of growing teamSkilled in troubleshooting and conducting multi-factorial experimentsGood numeracy, computer and communication skills Desirable Experience: Experience with cell isolation protocols from biological samplesFamiliarity with co-cultures and 3D culture systemsApplication of Design of Experiments (DoE) to rationalize experiment designExperience of writing SOPs and risk assessmentsRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Research Associate? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!The Research Associate will be working to to support the development of exciting new technologies to tackle a range of challenges associated with making our client's vision a reality. This is a lab-based role where you will be supporting the delivery of our research goals, the purpose of this role is to conduct scientific work to support the development of innovative technologies & processes. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Generate hypothesis and execute experiments related to R&D activities Analyse empirical data to identify significant results Feedback and present results to team Prepare reagents and perform analytical testing Generate SOPs, COSHH and other risk assessment documents  Participate in group R&D meetings  Maintain and organise laboratory consumables, reagents and equipment inventory  Ensure accurate recording of all experiments using electronic laboratory notebook  Laboratory maintenance (rota system)  Maintain the confidentiality of the project and protocols Qualifications: Degree in Life sciences, Genetics, Biotechnology, Biochemistry, Bioprocessing, Bioengineering, Material Science, Polymer Chemistry or related fieldExperience: Good understanding in the principles of your discipline Laboratory experience - at least one individual or shared project (including design and implementation of experiments) Good numeracy and problem-solving abilities Ability to communicate with a multi-disciplinary team Computer literate and ability to learn new software platforms Experience of experimental record-keeping Critical assessment of research articles  Data processing and statistical analysis And experience in one or more areas: Aseptic mammalian cell culture experience for adherent and/or suspension cell lines.  Molecular biology skillset in either DNA, protein or lipid characterisation Analysis of nutrient or metabolite content in culture media Experience in tissue engineering and/or working with biomaterials Set-up, running and harvesting of bioreactor Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Research Associate? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!The Research Associate will be working to to support the development of exciting new technologies to tackle a range of challenges associated with making our client's vision a reality. This is a lab-based role where you will be supporting the delivery of our research goals, the purpose of this role is to conduct scientific work to support the development of innovative technologies & processes. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Generate hypothesis and execute experiments related to R&D activities Analyse empirical data to identify significant results Feedback and present results to team Prepare reagents and perform analytical testing Generate SOPs, COSHH and other risk assessment documents  Participate in group R&D meetings  Maintain and organise laboratory consumables, reagents and equipment inventory  Ensure accurate recording of all experiments using electronic laboratory notebook  Laboratory maintenance (rota system)  Maintain the confidentiality of the project and protocols Qualifications: Degree in Life sciences, Genetics, Biotechnology, Biochemistry, Bioprocessing, Bioengineering, Material Science, Polymer Chemistry or related fieldExperience: Good understanding in the principles of your discipline Laboratory experience - at least one individual or shared project (including design and implementation of experiments) Good numeracy and problem-solving abilities Ability to communicate with a multi-disciplinary team Computer literate and ability to learn new software platforms Experience of experimental record-keeping Critical assessment of research articles  Data processing and statistical analysis And experience in one or more areas: Aseptic mammalian cell culture experience for adherent and/or suspension cell lines.  Molecular biology skillset in either DNA, protein or lipid characterisation Analysis of nutrient or metabolite content in culture media Experience in tissue engineering and/or working with biomaterials Set-up, running and harvesting of bioreactor Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Mechanical Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!As the Extrusion and Food Process Engineer, you will be the first member of the Bioprocess Engineering group that will be responsible for the design and implementation of our clients first-of-its-kind manufacturing processes and facilities. This position will design, build, test, and scale-up mechanical process equipment for cold extrusion and other specialty process applications. The role will require a strong background in machine design with the ultimate goal of deploying this equipment in our future commercial-scale manufacturing facilities and bringing strategic differentiation to our production platform.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Identify and define process and system requirements by understanding and challenging product formulation and processing assumptions with the aim of implementing robust unit operations and increasing overall operational efficiency and effectivenessPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsManaging relationships with strategic partners, engineering firms, equipment vendors and technology partnersSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsSome travel may be required to collaborator and manufacturing sitesAdditional ad hoc duties as required by the companyExperience: Ability to apply mechanical engineering principles and computer-aided methods to machine design and fabricationMechanical aptitude and comfortable with working directly on mechanical equipmentEfficient Design of Experiments and statistical analysis of experimental and characterization/validation dataUnderstanding of aseptic techniques and control of microbial contaminationAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsProject engineering and managementStrong scientific and technical writing and presentations.Detail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shootingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Mechanical Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!As the Extrusion and Food Process Engineer, you will be the first member of the Bioprocess Engineering group that will be responsible for the design and implementation of our clients first-of-its-kind manufacturing processes and facilities. This position will design, build, test, and scale-up mechanical process equipment for cold extrusion and other specialty process applications. The role will require a strong background in machine design with the ultimate goal of deploying this equipment in our future commercial-scale manufacturing facilities and bringing strategic differentiation to our production platform.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Identify and define process and system requirements by understanding and challenging product formulation and processing assumptions with the aim of implementing robust unit operations and increasing overall operational efficiency and effectivenessPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsManaging relationships with strategic partners, engineering firms, equipment vendors and technology partnersSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsSome travel may be required to collaborator and manufacturing sitesAdditional ad hoc duties as required by the companyExperience: Ability to apply mechanical engineering principles and computer-aided methods to machine design and fabricationMechanical aptitude and comfortable with working directly on mechanical equipmentEfficient Design of Experiments and statistical analysis of experimental and characterization/validation dataUnderstanding of aseptic techniques and control of microbial contaminationAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsProject engineering and managementStrong scientific and technical writing and presentations.Detail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shootingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • wicklow, international
      • permanent
      • randstad financial services
      Site Compliance and Product Release Lead Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D. Position SummaryThis position reports directly to the Site Quality Leader and will serve as the Quality Compliance and Product Release Manager for the Site. The Compliance and Product Release Lead will be the system owner for Auditing and Regulatory Inspection Management and have overall responsibility, working closely with the Quality Systems and Standards Lead, to ensure continuous site inspection readiness. The role will be responsible for Regulatory Compliance Surveillance and application for the Site QMS. Position ResponsibilitiesOversee Site License registration process.Approve Laboratory, Manufacturing and Packaging Master Batch Records.Ensure that Product release is in compliance with the registration files (QP) and fulfill the role of QP Batch Release Responsibility.Assuring Site Regulatory Compliance to Registrations via the Regulatory Change Management process, dossier harmonisation and working closely with Global Regulatory Affairs and Veterinary Medicines Research & Development (VMRA/VMRD) colleagues.Manage the timeliness and effectiveness of the Site completion and use of Annual Product Reviews (APRs).Lead the Site internal audit program, proactively identifying improvement opportunities and agreeing/prioritising improvement actions with Site stakeholders to ensure continuous inspection readiness.Lead Site regulatory inspections, preparation for and agreeing to remediation and CAPA plans with Regulatory Agencies.Consolidating outcomes and conducting risk assessment of BOH audits, GQCA audits, regulatory letters, manufacturing alerts and other relevant documents for the Site and its contractors or suppliers to identify trends and ensure CAPA plan is monitored, implemented, and effective.Leading the Site external contract service providers (CSP's) and suppliers audit program.Consolidating audit data for tracking/trending for compliance communications to Site and above site respective Leadership Teams.Responsible Contact for Site License Registration Process and Management of GMP Certificates.Assuring Site Regulatory Compliance to Registrations via the Regulatory Change Management process and execution of Lead Site Regulatory Role (compliance Network Member), working closely with Global Regulatory Affairs and Veterinary Medicines Research & Development (VMRA/VMRD) colleagues.Work with the site QSS Lead to Design, deploy and maintain compliant, robust, aligned, lean and efficient quality systems and tools at the site, which are aligned with Quality Risk Management Principles and which support GMS and commercial strategy, and support the product life cycle.Monitor Internal and External Factors Impacting the Pharmaceutical Quality System (i.e., emerging regulations, innovations that might enhance the pharmaceutical quality system).New Product Introduction - assure that all applicable quality aspects are met.Immediate notification to the Site Quality Head of any quality issues, and provide accurate and relevant information as required by the business.Serving as a quality culture role model and instil a strong quality and compliance culture across the site.Lead people development and succession plans for the Quality Compliance and Product Release function.Provide coaching/feedback to enhance the group and individual's professional performance and development,keeping succession plans updated to minimise hiring lags as roles become open in the group. Education, Qualifications and Experience Undergraduate degree in pharmaceutical, biological, chemical sciences, or engineering.Relevant advanced degree preferred.QP Eligibility desired.Minimum of 8 years progressive experience in the quality control, quality assurance, manufacturing operations in human or animal health. Current knowledge of cGMP's and demonstrated leadership of Regulatory Inspection Management and Regulatory Affairs.Recognised Lean Six Sigma Qualification (Green Belt or Black belt) desirable.Working knowledge of ICHQ10 key principles.Fluency in quality systems and regulatory compliance.Demonstrated ability in leading / managing people.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      Site Compliance and Product Release Lead Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D. Position SummaryThis position reports directly to the Site Quality Leader and will serve as the Quality Compliance and Product Release Manager for the Site. The Compliance and Product Release Lead will be the system owner for Auditing and Regulatory Inspection Management and have overall responsibility, working closely with the Quality Systems and Standards Lead, to ensure continuous site inspection readiness. The role will be responsible for Regulatory Compliance Surveillance and application for the Site QMS. Position ResponsibilitiesOversee Site License registration process.Approve Laboratory, Manufacturing and Packaging Master Batch Records.Ensure that Product release is in compliance with the registration files (QP) and fulfill the role of QP Batch Release Responsibility.Assuring Site Regulatory Compliance to Registrations via the Regulatory Change Management process, dossier harmonisation and working closely with Global Regulatory Affairs and Veterinary Medicines Research & Development (VMRA/VMRD) colleagues.Manage the timeliness and effectiveness of the Site completion and use of Annual Product Reviews (APRs).Lead the Site internal audit program, proactively identifying improvement opportunities and agreeing/prioritising improvement actions with Site stakeholders to ensure continuous inspection readiness.Lead Site regulatory inspections, preparation for and agreeing to remediation and CAPA plans with Regulatory Agencies.Consolidating outcomes and conducting risk assessment of BOH audits, GQCA audits, regulatory letters, manufacturing alerts and other relevant documents for the Site and its contractors or suppliers to identify trends and ensure CAPA plan is monitored, implemented, and effective.Leading the Site external contract service providers (CSP's) and suppliers audit program.Consolidating audit data for tracking/trending for compliance communications to Site and above site respective Leadership Teams.Responsible Contact for Site License Registration Process and Management of GMP Certificates.Assuring Site Regulatory Compliance to Registrations via the Regulatory Change Management process and execution of Lead Site Regulatory Role (compliance Network Member), working closely with Global Regulatory Affairs and Veterinary Medicines Research & Development (VMRA/VMRD) colleagues.Work with the site QSS Lead to Design, deploy and maintain compliant, robust, aligned, lean and efficient quality systems and tools at the site, which are aligned with Quality Risk Management Principles and which support GMS and commercial strategy, and support the product life cycle.Monitor Internal and External Factors Impacting the Pharmaceutical Quality System (i.e., emerging regulations, innovations that might enhance the pharmaceutical quality system).New Product Introduction - assure that all applicable quality aspects are met.Immediate notification to the Site Quality Head of any quality issues, and provide accurate and relevant information as required by the business.Serving as a quality culture role model and instil a strong quality and compliance culture across the site.Lead people development and succession plans for the Quality Compliance and Product Release function.Provide coaching/feedback to enhance the group and individual's professional performance and development,keeping succession plans updated to minimise hiring lags as roles become open in the group. Education, Qualifications and Experience Undergraduate degree in pharmaceutical, biological, chemical sciences, or engineering.Relevant advanced degree preferred.QP Eligibility desired.Minimum of 8 years progressive experience in the quality control, quality assurance, manufacturing operations in human or animal health. Current knowledge of cGMP's and demonstrated leadership of Regulatory Inspection Management and Regulatory Affairs.Recognised Lean Six Sigma Qualification (Green Belt or Black belt) desirable.Working knowledge of ICHQ10 key principles.Fluency in quality systems and regulatory compliance.Demonstrated ability in leading / managing people.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003

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