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- Tasks: Lead validation and compliance for cutting-edge medical equipment and software.
- Company: Join Convatec, a global leader in innovative medical solutions.
- Benefits: Enjoy hybrid working, competitive salary, and professional growth opportunities.
- Other info: Be part of a dynamic team in a vibrant life sciences ecosystem.
- Why this job: Make a real difference in healthcare while working with advanced technologies.
- Qualifications: 5 years' experience in lab equipment validation and a relevant degree required.
The predicted salary is between 42000 - 60000 £ per year.
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs.
The Senior Equipment Specialist will be responsible for the completion of all validation and compliance activities relating to the purchase of new and updating of existing equipment/software located within the Laboratories at Convatec Global Development Centre (GDC). The Senior Equipment Specialist should be detail-oriented, able to work on multiple projects and adapt to changes, with good problem-solving skills and strong communication are essential.
- Participate in Equipment/Software Validation activities (e.g., Analyze data and prepare technical reports as needed).
- Support software validation activities for laboratory systems, ensuring Data Integrity compliance and implementing remedial action plans.
- Support implementation and maintenance of laboratory informatics software/platforms and lab enterprise systems.
- Thorough knowledge of quality and regulatory requirements (ISO13485, cGMP) in Medical Device/Pharmaceutical industries.
- Expertise in laboratory equipment/software validation, calibration, and maintenance, including 21 CFR Part 11.
- Previous experience with the use of electronic data management systems.
- Flexible and responsive to changing priorities and ad-hoc requests.
- Degree in relevant science or engineering field, plus 5 years' experience in laboratory equipment validation/calibration in Medical Device/Pharmaceutical Industry.
- Experience with software validations, 21 CFR Part 11, and calibration management systems.
- Proficiency in Microsoft Office and database applications.
- Hybrid working role based in Deeside in 2026, moving to Manchester in 2027. Combination of laboratory and office environments.
- Exposure to chemicals, reagents, and biological agents within laboratory areas.
- Option for up to 2 days of remote work per week after role establishment, with minimal travel (5-10 days annually).
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 Validations Officer in Manchester employer: Convatec
Contact Detail:
Convatec Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Validations Officer in Manchester
✨Tip Number 1
Networking is key! Reach out to current or former employees at Convatec on LinkedIn. A friendly chat can give us insights into the company culture and maybe even a referral!
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of ISO13485 and cGMP regulations. We want to show that we’re not just familiar with the requirements but can also apply them in real-world scenarios.
✨Tip Number 3
Practice common interview questions related to validation and compliance. We can role-play with a friend or use online resources to get comfortable discussing our experience and skills.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows we’re serious about joining the Convatec team!
We think you need these skills to ace Senior Validations Officer in Manchester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Validations Officer role. Highlight your experience in laboratory equipment validation and compliance, and don’t forget to mention any relevant qualifications or certifications that align with the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about improving lives through medical solutions. Share specific examples of your problem-solving skills and how you've adapted to changes in previous roles.
Showcase Your Technical Skills: Since this role requires expertise in software validation and regulatory requirements, make sure to showcase your technical skills clearly. Mention your familiarity with ISO13485, cGMP, and 21 CFR Part 11 to demonstrate your fit for the position.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Convatec
✨Know Your Stuff
Make sure you brush up on your knowledge of ISO13485, cGMP, and 21 CFR Part 11. Being able to discuss these regulations confidently will show that you’re not just familiar with the requirements but also understand their importance in the medical device industry.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experience where you successfully tackled challenges related to equipment validation or compliance. Convatec values strong problem-solving abilities, so having specific scenarios ready will help demonstrate your capability.
✨Be Ready for Technical Questions
Expect some technical questions about laboratory equipment and software validation. Brush up on your technical knowledge and be prepared to explain your thought process when validating systems or handling data integrity issues.
✨Emphasise Adaptability
Since the role requires flexibility and responsiveness to changing priorities, think of instances where you’ve had to adapt quickly in a work environment. Sharing these experiences will highlight your ability to thrive in a dynamic setting like Convatec’s.