Latest Biomedical Jobs at Olympus Corporation | Apply Now for Regulatory Affairs Specialist Role
Are you looking for a meaningful role in the medical device industry where your expertise in regulatory affairs can drive real-world impact? Olympus Corporation is hiring a Regulatory Affairs Specialist at its Southend-On-Sea location in Essex. Join a global leader in medical technology, known for its century-long commitment to health, safety, and innovation. If you have a strong background in regulatory compliance and a passion for improving lives, this opportunity is your next big move.
About the Company
Welcome to Olympus Corporation, a global leader in the medical device and technology industry. For over 100 years, Olympus has been dedicated to improving people’s lives by focusing on health, safety, and fulfillment. Our innovative products and solutions are instrumental in diagnosing, preventing, and treating illnesses, supporting scientific research, and ensuring safety. Olympus Corporation is a global leader in medical technology, dedicated to making people’s lives healthier, safer, and more fulfilling for over a century. With expertise in medical devices, life sciences, and industrial solutions, Olympus is at the forefront of diagnosing, preventing, and treating disease. Our innovations empower healthcare professionals to deliver better patient outcomes, while our global team of nearly 31,000 employees drives a culture of integrity, empathy, and continuous improvement. At Olympus, we believe in creating technology that transforms care and improves lives—every day.
Job Details
Job Post: Regulatory Affairs Specialist
Company: KeyMed (Medical & Industrial Equipment) Ltd. (OKM) | Chief Quality Officer
Type of Employment: Permanent
Function: Quality / Audit / Corporate Governance
Location: Southend-On-Sea, Essex, England
Qualifications
- University degree in a scientific subject, such as Biomedical Science, Pharmacy, Engineering, or a similar discipline.
- Minimum 2 years’ experience in regulatory affairs, quality, or R&D in the medical device industry
- Good understanding of the medical device regulatory framework
- Experience in change management
- Strong communication, negotiation, and organizational skills
- Ability to work effectively in a team
- Proficiency in the MS Office suite
Responsibilities
- Implement regulatory and quality requirements
- Adhere to Health, Safety, and Environmental standards
- Generate and maintain technical documentation for compliance
- Initiate change requests for portfolio updates
- Review product/process change requests
- Support regulatory compliance projects
- Drive process updates and improvement
- Own change management in product design
Competencies
- Patient Focus – We put patients at the heart of everything
- Integrity – We do the right thing
- Innovation – We look for new ways to make things better
- Impact – We take accountability and get things done
- Empathy – We care for one another and work together
Benefits
- Competitive salary
- Generous annual leave entitlement
- Private medical cover
- Comprehensive company pension scheme
- Annual health check with BUPA
- Employee Assistance Program
- Subsidized staff restaurant and free parking
- Discounted gym and wellness memberships
Reference Number: 80039684-04022025
Website: https://www.olympus.co.uk
Keywords: Olympus Corporation, Regulatory Affairs Specialist, Latest Biomedical Jobs at Olympus, Medical Device Industry, Quality, Compliance, Job Posting
