- Title: Multi-skilled Maintenance Engineer (Days Shifts)Location: Brentwood, EssexShifts: Monday - Friday, Double Days (6am-2pm/2pm-10pm)Salary: Circa £48,000 - £50,000 + Overtime (x1.5/x2) + Annual Bonus + Contributory Pensions + Industry Training + 33 Days Holidays The Role:My client is an international pharmaceutical manufacturer that is seeking a senior multi-skilled maintenance engineer with experience within a FMCG manufacturing industry or similar woTitle: Multi-skilled Maintenance Engineer (Days Shifts)Location: Brentwood, EssexShifts: Monday - Friday, Double Days (6am-2pm/2pm-10pm)Salary: Circa £48,000 - £50,000 + Overtime (x1.5/x2) + Annual Bonus + Contributory Pensions + Industry Training + 33 Days Holidays The Role:My client is an international pharmaceutical manufacturer that is seeking a senior multi-skilled maintenance engineer with experience within a FMCG manufacturing industry or similar wo
- ResponsibilitiesPerform routine and non-routine microbiological testing with accurate documentation.Manage lab operations: scheduling, equipment, stock control, and maintenance.Ensure a safe, compliant lab environment aligned with SOPs and quality standards.Maintain quality systems (cGLP), including SOPs, validations, investigations, and trend reviews.Collaborate cross-functionally to support projects and continuous improvement.Lead contamination control eResponsibilitiesPerform routine and non-routine microbiological testing with accurate documentation.Manage lab operations: scheduling, equipment, stock control, and maintenance.Ensure a safe, compliant lab environment aligned with SOPs and quality standards.Maintain quality systems (cGLP), including SOPs, validations, investigations, and trend reviews.Collaborate cross-functionally to support projects and continuous improvement.Lead contamination control e
- ResponsibilitiesDeveloping dashboards, examining data, and compiling reports for business discussions.Stay up to date with market trends to identify new lead opportunities.Support the team with increasing effectiveness of business development initiatives.Identify process improvement opportunities to promote team productivity and operational goals.Building partnerships with new and existing clients.RequirementsKnowledge of the pharmaceutical industry or relResponsibilitiesDeveloping dashboards, examining data, and compiling reports for business discussions.Stay up to date with market trends to identify new lead opportunities.Support the team with increasing effectiveness of business development initiatives.Identify process improvement opportunities to promote team productivity and operational goals.Building partnerships with new and existing clients.RequirementsKnowledge of the pharmaceutical industry or rel
- Are you a skilled and motivated individual with an engineering background looking for a challenging and rewarding role with a leading medical technology company? A global leader in medical technology, is seeking a dynamic Moulding Production Technician to join a team in Plymouth. You'll be part of a cutting-edge manufacturing operation, playing a vital role in producing millions of life-saving medical devices each year. What You'll Do: Precision ManufacturAre you a skilled and motivated individual with an engineering background looking for a challenging and rewarding role with a leading medical technology company? A global leader in medical technology, is seeking a dynamic Moulding Production Technician to join a team in Plymouth. You'll be part of a cutting-edge manufacturing operation, playing a vital role in producing millions of life-saving medical devices each year. What You'll Do: Precision Manufactur
- ResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.ActResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.Act
