- Are you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of our clients regulatory project team representing Middle East Africa, Turkey, CIS & Russia and Central Eastern European Markets in the International Growth Markets team with accountability for 1-3 products progressing through NDA planning, filing and appAre you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of our clients regulatory project team representing Middle East Africa, Turkey, CIS & Russia and Central Eastern European Markets in the International Growth Markets team with accountability for 1-3 products progressing through NDA planning, filing and app
- Are you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of the Global Regulatory Project team representing the international Growth markets with accountability for 1-3 marketed products across APAC, MART CEER and LatAm. You will be developing and implementing regulatory strategies to support product lifecycle maAre you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of the Global Regulatory Project team representing the international Growth markets with accountability for 1-3 marketed products across APAC, MART CEER and LatAm. You will be developing and implementing regulatory strategies to support product lifecycle ma
- Do you have a passion for making a positive impact on the environment and the lives of others? As a QESH Coordinator, you will play a vital role in ensuring our operations comply with all relevant regulations and standards. Our client manufactures, distributes, sells and markets some of the world's strongest brands in non-alcoholic beverages. It is a leading Western European marketer, distributor, and producer of bottles and can non-alcoholic refreshment.Do you have a passion for making a positive impact on the environment and the lives of others? As a QESH Coordinator, you will play a vital role in ensuring our operations comply with all relevant regulations and standards. Our client manufactures, distributes, sells and markets some of the world's strongest brands in non-alcoholic beverages. It is a leading Western European marketer, distributor, and producer of bottles and can non-alcoholic refreshment.
- Are you detail-oriented and passionate about quality assurance?Do you thrive in a fast-paced environment where your contributions make a real difference?Do you have experience in administrative roles with a focus on compliance and process improvement?If so, we have an exciting opportunity for you!Join a leading global medical device and healthcare company as a Medical Devices Compliance Technician in Sittingbourne, Kent!In this vital role, you will:ChampioAre you detail-oriented and passionate about quality assurance?Do you thrive in a fast-paced environment where your contributions make a real difference?Do you have experience in administrative roles with a focus on compliance and process improvement?If so, we have an exciting opportunity for you!Join a leading global medical device and healthcare company as a Medical Devices Compliance Technician in Sittingbourne, Kent!In this vital role, you will:Champio
- ResponsibilitiesEnsure regulatory compliance through audits, monitoring systems, and up-to-date documentation.Manage systems, including document control, policy updates, and staff acknowledgements.Support inspections and mock audits with internal teams and external regulatory bodies.Assist in implementing and tracking quality improvement plans across all departments.Oversee daily incident reviews, support risk assessments, and promote a strong reporting cuResponsibilitiesEnsure regulatory compliance through audits, monitoring systems, and up-to-date documentation.Manage systems, including document control, policy updates, and staff acknowledgements.Support inspections and mock audits with internal teams and external regulatory bodies.Assist in implementing and tracking quality improvement plans across all departments.Oversee daily incident reviews, support risk assessments, and promote a strong reporting cu
- 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
