Work Schedule
First Shift (Days)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting No contact lens allowed; prescriptive glasses will be provided Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job Description
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.
Position is based Manati Puerto Rico. Position will support our Drug Product Division (DPD) at Thermo Fisher Scientific.
Lead a Quality Control team responsible for ensuring product excellence and regulatory compliance at Thermo Fisher Scientific. Implement analytical testing method validation and quality systems while supporting a culture of continuous improvement. Collaborate with cross-functional teams to deliver high-quality products that help make the world healthier cleaner and safer.
Oversee testing operations including raw materials in-process controls environmental monitoring and finished product release.
Support data integrity and Good Manufacturing Practices (GMP) while developing team members through mentoring and training.
Ensure laboratory readiness for regulatory inspections and customer audits while improving operational efficiency through quality metrics and process improvements.
Keys to Success:
BS Degree required. Preferred Fields of Study: Chemistry Biology Biochemistry Pharmaceutical Sciences or related scientific field.
Advanced degree preferred.
Advanced degree plus 6 years of experience or Bachelors degree plus 8 years of experience in regulated pharmaceutical or biotech industry quality control.
5 years of people management experience leading QC laboratory teams.
Experience managing laboratory investigations deviations and CAPA processes.
Experience with laboratory information management systems (LIMS) and data integrity requirements.
Experience supporting regulatory inspections and customer audits.
Knowledge Skills Abilities
Extensive knowledge of cGMP regulations quality systems and regulatory requirements (FDA EMA ICH)
Strong understanding of analytical testing methods and laboratory operations
Demonstrated success implementing and improving quality systems and processes
Leadership experience developing and mentoring staff
Project management and organizational skills
Clear written and verbal communication skills
Proficiency with standard business software (MS Office) and quality systems
Ability to adapt to changing priorities
Problem-solving skills and scientific decision-making abilities
Commitment to workplace safety and compliance
Client Communications ability
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:
Manager
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more