At a Glance
- Tasks: Lead a team in delivering biocompatibility evaluations for innovative medical devices.
- Company: Join a forward-thinking company committed to improving healthcare.
- Benefits: Enjoy remote work, competitive salary, and opportunities for professional growth.
- Other info: Collaborative culture with global travel opportunities and flexible working conditions.
- Why this job: Make a real impact in the medical field while developing your leadership skills.
- Qualifications: 10+ years in biocompatibility assessments and a relevant degree.
The predicted salary is between 60000 - 80000 £ per year.
Position Overview
The Senior Manager of Biocompatibility leads a team of biocompatibility specialists in delivering biological evaluations in line with ISO 10993 standards or the equivalent from regulated markets globally across our four categories (Ostomy Care, Infusion Care, Advanced Wound Care and Continence Care). The biocompatibility team supports New Product Development (NPD) and Lifecycle Management (LCM) projects, and consults on early‑stage developments. Biocompatibility is an integrated part of project teams and has a critical role in delivering timely and effective biological evaluations for new products and in evaluating changes to existing products. The team also partners closely with the Regulatory and Medical / Clinical teams. Fostering effective collaboration is a critical part of the role.
The Senior Manager of Biocompatibility is responsible for coaching and developing the team to maintain up to date knowledge of global medical device standards and regulations as well as keep abreast of the state of the art within the field.
Key Responsibilities
- Manages and allocates resources in line with project needs and priorities
- Identifies training opportunities for the team towards continuous improvement
- Ensures seamless and proactive collaboration with the project teams
- Synthesises a development plan with each team member
- Ensures the team has up to date knowledge of biocompatibility standards, techniques and protocols
- Instills a positive working culture of collaboration in line with Convatec’s values and leadership behaviors
- Fosters cross‑functional collaboration and teamwork between the biocompatibility team, the business units, project teams, regulatory and clinical teams
- Leads on accurate project planning and timely execution in partnership with project teams to keep biocompatibility activities visible and integrated into overall project plans
- Works closely with program/project cross‑functional teams to provide biocompatibility deliverables in compliance with global regulatory requirements
- Evaluates and executes biocompatibility studies in support of programs dealing with our medical devices
- Approaches problem solving creatively with detailed knowledge of ISO standard testing
- Identifies, obtains stakeholder buy‑in and implements continuous process improvements and learning
- Supports biological hazards risk analysis activities
- Analyzes, interprets, and draws conclusions from biocompatibility testing, including but not limited to extractable and leachable chemical characterization and biological evaluations
- Delivers to company quality metrics (CAPA, NC, IA, etc.)
Skills & Experience
- 10+ years experience in biocompatibility assessments for NPDs and LCMs in territories including Europe and USA
- Experience with complex FDA submissions and dealing with FDA queries and feedback is essential
- 10+ years’ industrial experience in the field of Medical Device, Pharmaceutical, or Biotechnology with expertise in biocompatibility, toxicology, related principles and industry standards
Qualifications/Education
- BSc or higher degree in one or more of the following disciplines: Biomedical Engineering, Bioengineering, Biology (Biological Sciences), Molecular Cell Biology, Biochemistry, Microbiology, or Toxicology; advanced degree (MS or PhD) in these fields preferred
Additional Information
- Team: 6 Direct Reports
- Travel Requirements: Position may involve travel around 25% of the time, mostly within Europe but overseas travel is expected.
- Working Conditions: Remote working from home with presence in the office on a weekly or monthly basis driven by business requirements.
- Special Factors: May need to support global discussions in different time zones.
Equal opportunities: Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Senior Manager Biocompatibility in Manchester employer: Convatec
At Convatec, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As a Senior Manager of Biocompatibility, you will lead a dedicated team while benefiting from continuous professional development opportunities and a commitment to employee well-being. With a flexible remote working arrangement and a focus on diversity and inclusion, Convatec offers a rewarding environment where your expertise in biocompatibility can thrive and make a meaningful impact in the medical device industry.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Manager Biocompatibility in Manchester
✨Tip Number 1
Network like a pro! Reach out to your connections in the biocompatibility field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on ISO 10993 standards and recent advancements in biocompatibility. Show off your knowledge and passion during the interview – it’ll set you apart from the competition!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and expertise. Check out our website for openings that match your skills in biocompatibility and make sure to tailor your approach to each one.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Plus, it shows your enthusiasm for the role and the company culture.
We think you need these skills to ace Senior Manager Biocompatibility in Manchester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your experience in biocompatibility and medical devices. We want to see how your background aligns with the key responsibilities mentioned in the job description.
Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for the Senior Manager role. Share specific examples of your leadership and collaboration skills, especially in biocompatibility projects.
Showcase Your Knowledge:Demonstrate your understanding of ISO 10993 standards and other relevant regulations in your application. We’re looking for someone who can hit the ground running, so let us know how you stay updated in this field.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at Convatec
✨Know Your Standards
Make sure you’re well-versed in ISO 10993 standards and any relevant regulations. Brush up on the latest updates in biocompatibility testing and be ready to discuss how these standards apply to the role. This shows you’re not just familiar with the basics but are also proactive about staying current.
✨Showcase Your Leadership Skills
As a Senior Manager, you’ll need to demonstrate your ability to lead and develop a team. Prepare examples of how you’ve coached team members or fostered collaboration in past roles. Highlight specific instances where your leadership made a difference in project outcomes.
✨Prepare for Cross-Functional Collaboration
Since this role involves working closely with various teams, think of examples that showcase your experience in cross-functional collaboration. Be ready to discuss how you’ve successfully partnered with regulatory and clinical teams in the past to achieve project goals.
✨Problem-Solving Mindset
Expect questions that assess your problem-solving abilities, especially in relation to biocompatibility challenges. Prepare to discuss specific problems you’ve encountered in previous projects and how you creatively approached solutions, particularly in line with ISO standards.
