Validation Manager
Thermo Fisher Scientific
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Fluctuating Temps hot/cold Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) WarehouseJob Description
Title: Validation Manager
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Division/Site Specific Information
Role reports to the Allentown PA site and reports to the Clinical Trials Division (CTD). CTD partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time a concept that we internally embrace as There is a Patient Waiting. Our outstanding blend of services includes project management packaging distribution transportation management and specialty logistics ancillary supply management clinical supply optimization bio-repository storage and much more.
Our more than 3000 employees in over 15 countries work hard every day knowing that what they do matters.
Discover Impactful Work:
As a Validation Manager at Thermo Fisher Scientific you will manage validation activities that ensure product quality and regulatory compliance. Youll develop validation strategy and oversee a team responsible for qualifying equipment utilities facilities computer systems and manufacturing processes.
A Day in the Life
- Working across functions youll ensure validation activities align with cGMP requirements while supporting new product introductions and technology transfers.
- This role offers the opportunity to make a meaningful impact by maintaining the validated state of systems that help produce therapeutics.
Keys to Success:
Education/Experience
- Advanced Degree plus 4 years of experience or Bachelors Degree plus 6 years of experience in validation in pharmaceutical/biotech manufacturing or related regulated industry required.
- Preferred Fields of Study: Engineering Science Chemistry Biology or related technical discipline.
- 3 years of people management or team leadership experience.
- Experience with equipment process cleaning computer system and utility validation - temperature mapping experience preferred
- Experience with data integrity evaluation and knowledge of ALCOA principles
- Experience participating in regulatory inspections and customer audits
- Experience with validation master planning and change control systems
Knowledge Skills Abilities
- Expertise in risk assessment methodologies and statistical analysis
Demonstrated success managing complex validation projects and programs - Strong knowledge of cGMP regulations particularly FDA and EU requirements
- Proficiency with quality systems and validation documentation
- Excellent technical writing and documentation skills
- Strong leadership communication and interpersonal abilities
- Ability to influence and collaborate across functions and levels
- Knowledge of lean/continuous improvement methodologies
- Proficient with standard business software applications
- Travel up to 10% as needed
Benefits
We offer competitive remuneration annual incentive plan bonus scheme healthcare and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative forward-thinking organization and outstanding career and development prospects. We offer an exciting company culture that stands for integrity intensity involvement and innovation.
Required Experience:
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