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- Tasks: Lead validation activities and ensure compliance in a dynamic pharmaceutical environment.
- Company: Join Ferring, a leader in reproductive medicine and women’s health.
- Benefits: Enjoy competitive salary, performance bonuses, and comprehensive family-building benefits.
- Why this job: Make a real impact on healthcare while growing your career in a supportive team.
- Qualifications: Degree in science or engineering with 3 years in pharmaceutical production preferred.
- Other info: Flexible working hours and excellent career growth opportunities await you.
The predicted salary is between 36000 - 60000 £ per year.
Ferring Controlled Therapeutics is a pharmaceutical manufacturing and development organisation located in East Kilbride. We are committed to building families and helping people live better lives and are leaders in reproductive medicine and women’s health.
Now is an exciting time to join us in our current growth phase. For this varied and dynamic role, we are seeking someone with a can-do attitude and a positive mindset to maintain and continuously improve our validation activities. The successful candidate will work cross functionally qualifying new packaging lines and ancillary equipment in our new facility in East Kilbride.
We are offering a permanent, full time role which includes a competitive salary, annual performance bonus, company pension, life assurance, private medical care and onsite parking. We also offer 25 days annual leave + 9 public holidays.
Job Description:- Lead and carry out validation activities throughout the facility
- Create Validation Schedule and provide monthly updates
- Ensure validation status for all GxP systems including equipment, processes, utilities and cleaning
- Update site validation SOP’s as required
- Prepare validation protocols and reports
- Carry out Process Performance Qualification & Continuous Process Verification
- Perform Computerised System Validations including Computerised system assessments, Data Integrity assessments
- Carry out GxP Risk Assessments for Equipment/Product changes or repairs
- Support and prepare Change Controls, CAPA’s and Deviations
- Liaise with vendors during new equipment Design and FAT/SAT stages
- Review vendor validation packages for completeness, accuracy and compliance to validation policies
- Carry out temperature mapping of product storage areas
- Degree level in a scientific or engineering discipline
- 3 years’ experience with pharmaceutical production preferred
- Knowledge of GMP preferred
- Excellent computer skills including Microsoft office and Minitab
- Good communication and teamwork skills
- Excellent attention to detail and organisational skills
- Performance Bonus scheme
- Company pension
- Life insurance
- On-site parking
- Private dental insurance
- Private medical insurance
- Monday to Friday, 37.5 hrs per week
- Core business hours 08:30 to 16:30, with flexitime
- Pharmaceutical or Highly Regulated: 1 year (preferred)
Validation Engineer in East Kilbride employer: Ferring Holding SA
Contact Detail:
Ferring Holding SA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Engineer in East Kilbride
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and practising common questions. Show them you’re not just another candidate; you’re genuinely interested in Ferring and what they do!
✨Tip Number 3
Follow up after your interview with a thank-you email. It’s a simple gesture that shows your appreciation and keeps you fresh in their minds. Plus, it’s a great chance to reiterate your enthusiasm for the role!
✨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, we love seeing candidates who take that extra step!
We think you need these skills to ace Validation Engineer in East Kilbride
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Validation Engineer role. Highlight relevant experience and skills that match the job description, like your knowledge of GMP and validation activities.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your enthusiasm for the role and the company. Mention how your can-do attitude aligns with Ferring's mission to help people live better lives.
Showcase Your Attention to Detail: As a Validation Engineer, attention to detail is key. In your application, provide examples of how you've demonstrated this skill in past roles, especially in validation or compliance settings.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way to ensure your application gets the attention it deserves, and we can’t wait to see what you bring to the team!
How to prepare for a job interview at Ferring Holding SA
✨Know Your Validation Basics
Make sure you brush up on your knowledge of validation processes, especially in a pharmaceutical context. Understand GxP regulations and be ready to discuss how you've applied these principles in past roles.
✨Showcase Your Teamwork Skills
Since the role involves cross-functional collaboration, prepare examples that highlight your ability to work well with others. Think of specific instances where you successfully liaised with different teams or vendors.
✨Prepare for Technical Questions
Expect questions about specific validation activities like Process Performance Qualification or Computerised System Validations. Be ready to explain your experience with these processes and any tools you've used, such as Minitab.
✨Demonstrate Your Attention to Detail
Validation requires a keen eye for detail. Prepare to discuss how you ensure accuracy in your work, perhaps by sharing examples of how you've caught errors or improved processes in previous positions.
