At a Glance
- Tasks: Lead biocompatibility evaluations and generate reports to ensure product safety.
- Company: Join CooperVision, a global leader in contact lens manufacturing, dedicated to improving vision.
- Benefits: Enjoy 25 days holiday, private medical insurance, wellness support, and career development opportunities.
- Why this job: Be part of a diverse team making a real impact on people's lives through innovative products.
- Qualifications: BSc in biological science or related field; experience with ISO 10993 is essential.
- Other info: Work in a supportive environment that values inclusion and personal growth.
The predicted salary is between 36000 - 60000 £ per year.
Department: UK R&D Chemistry
Location: Chandlers Ford, Eastleigh
GLS: T03
Working hours: Monday to Friday 37.5 hours per week Onsite
A brighter future awaits you. CooperVision is one of the world’s leading manufacturers of soft contact lenses with a presence in over 100 countries. Being part of CooperVision means helping improve the way people see each day. It’s more than making contact lenses, it’s about giving lens wearers freedom and confidence to move about their daily lives. We’re all about bright futures – for our people and those who wear our contact lenses.
At CooperVision, we’re big on belonging. Everyone’s contribution counts, and that’s why inclusion and diversity are so important. It isn’t just the right thing to do; it’s what makes our company the best it can be. We are committed to creating an inclusive and engaging workplace. Our Employee Resource Groups offer employees to grow within a safe and inclusive space. So be yourself, whoever you are, and let’s achieve amazing things together.
Job summary – What to expect:
We have an exciting permanent opportunity for a Senior Scientist – Biocompatibility with a particular focus on Biological Evaluation. In this role, you will be responsible for generating, maintaining, and updating Biological Evaluation Reports (BERs) per EU MDR requirements. The role focusses on the toxicological and biocompatibility evaluation of products and technologies required for product approvals and the establishment of patient safety of medical devices in accordance with applicable global regulatory guidelines.
Additionally, the senior scientist will provide support to enable the delivery of toxicological risk assessments for different projects, process change assessments, material quality assessments including material supplier contamination, innovation projects and support to regulatory projects.
Key responsibilities include:
- Compile and deliver biocompatibility assessments and biocompatibility evaluation plans and reports in compliance with applicable biological evaluation standards and guidance documents.
- Generation and maintenance of Biological Evaluation Reports to meet EU MDR regulations.
- Perform and assist with risk assessments and gap analysis of external standards, regulatory requirements, and guidance documents associated with biological safety evaluation.
- Collaborate with cross-functional teams to support projects requiring biocompatibility evaluation and ensure timely completion to meet established deadlines.
- Keep abreast of regulatory requirements including monitoring EU MDR, FDA and other agency regulations and international standards with respect to biological evaluation.
- Prepare or collaborate in the preparation of toxicological safety assessments including materials, chemicals, technologies and processes or finished products.
- Work within multi-disciplinary teams (notably R&D, HS&E, Import/Export, Supply Chain and RA/QA) on a variety of activities as required by the business.
- Ensure due process is followed under R&D Policies and Framework.
- Support the creation and development of the strategy for biological/toxicological evaluation (including testing requirements) for materials and finished products.
- Provide technical support and coaching for members of R&D, regulatory or any other relevant department.
- Provide consultancy on technical issues both within R&D and other stakeholders.
A Full Job Description Is Available Upon Request.
About you:
We are looking for someone who is a strong team player with good stakeholder engagement skills who can bring with them the following experience:
- Either a BSc in a biological science (Pharmacology, Biology, Physiology, Biochemistry or similar) or related discipline (MSc in Toxicology or any work-related experience in toxicology a bonus).
- Industrial experience within the chemical area (Medical device / pharmaceutical preferred) depending on degree level.
- Direct experience working with ISO 10993 is essential.
- Demonstrated success in leading change in particular for the implementation of ISO 10993 standards series is essential.
- Working knowledge of domestic and international regulations and standards that affect Class II and III medical device compliance is essential.
What we offer:
You’ll receive competitive compensation and a fantastic benefits package including 25 days holiday, Private medical insurance, pension scheme, healthcare cover, life assurance, access to our Wellness Platform to support you in mental health and wellbeing, a discounted contact lens scheme and much more!
We are committed to our employees’ personal and professional development and offer extensive training to support your career growth and help every individual to reach their full potential. To help us achieve our goals, we’ll give you everything you need to help you achieve yours.
We also provide access to LinkedIn Learning to help you develop in your career and grow with CooperVision.
What you can expect:
As a CooperVision employee, you’ll be welcomed into a diverse and progressive global business. We appreciate how important fostering a diverse and inclusive culture is and how different perspectives add value and contribute to our success. With our CooperPride, African Descent, Woman’s Impact Network and Mind Body and Wellbeing Employee Resource Groups, we offer opportunities for employees to learn and grow within an inclusive and safe space.
If you like what you see, take the first step towards your Brighter Future and apply today! All suitably qualified applicants will receive equal consideration and opportunities from CooperVision.
Please view our careers page at https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1 to view all other opportunities.
Qualifications
About Us
CooperVision is a global leader in the contact lens industry, dedicated to helping improve the way people see every day. Achieving that goal takes the collaboration of team members with wide-ranging skills; from scientists and researchers, to manufacturing and operations experts, to sales and marketing professionals.
At CooperVision, our effort to improve lives begins with our employees. We are committed to developing people as a key global differentiator and our most important asset. We empower employees to succeed, rewarding great thinking and hard work with competitive pay, comprehensive benefits, and with a special focus on wellness. Our commitment to our core values and an employee-centric culture fuel a deeply engaged, high performing organization.
CooperVision employees pride themselves on being proactive, innovative, flexible and friendly. That’s a strong reflection of our corporate culture—and part of the reason CooperVision may be a great workplace for you.
Senior Scientist, Biocompatibility (Biological Evaluation) employer: CooperVision
Contact Detail:
CooperVision Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Scientist, Biocompatibility (Biological Evaluation)
✨Tip Number 1
Familiarise yourself with ISO 10993 standards, as direct experience with these is essential for the role. Consider reviewing case studies or recent publications that highlight successful implementations of these standards in biocompatibility evaluations.
✨Tip Number 2
Network with professionals in the medical device and pharmaceutical industries. Attend relevant conferences or webinars to connect with others who have insights into the biocompatibility field, which could lead to valuable referrals or recommendations.
✨Tip Number 3
Stay updated on the latest regulatory changes regarding biological evaluation and safety assessments. Subscribing to industry newsletters or joining professional organisations can provide you with timely information that may impress during interviews.
✨Tip Number 4
Prepare to discuss your experience with cross-functional collaboration. Think of specific examples where you've worked with teams from different departments, as this role requires strong stakeholder engagement skills.
We think you need these skills to ace Senior Scientist, Biocompatibility (Biological Evaluation)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in biocompatibility and toxicology. Emphasise any direct experience with ISO 10993 and your understanding of regulatory requirements for medical devices.
Craft a Compelling Cover Letter: In your cover letter, express your passion for the role and the company. Mention specific projects or experiences that align with the responsibilities outlined in the job description, particularly your ability to compile and deliver biocompatibility assessments.
Showcase Team Collaboration Skills: Since the role involves working within multi-disciplinary teams, provide examples of past collaborations. Highlight how you effectively engaged with stakeholders and contributed to successful project outcomes.
Highlight Continuous Learning: Mention any ongoing professional development, such as courses or certifications related to biocompatibility or toxicology. This shows your commitment to staying updated with industry standards and regulations.
How to prepare for a job interview at CooperVision
✨Know Your Standards
Familiarise yourself with ISO 10993 and other relevant biocompatibility standards. Be prepared to discuss how your experience aligns with these regulations, as this will demonstrate your expertise in the field.
✨Showcase Team Collaboration
Highlight your experience working within multi-disciplinary teams. CooperVision values collaboration, so share specific examples of how you've successfully engaged with different stakeholders to achieve project goals.
✨Stay Updated on Regulations
Make sure you are up-to-date with the latest EU MDR and FDA regulations. Being knowledgeable about current guidelines will show your commitment to compliance and patient safety, which is crucial for this role.
✨Prepare for Technical Questions
Expect technical questions related to toxicological risk assessments and biological evaluation reports. Brush up on your knowledge in these areas and be ready to discuss your previous work and its impact on product approvals.