Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll 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 world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

 

How will you make an impact?

Investigates and observes Operations and Quality Operations departments to assure that FDA current Good Manufacturing Practices, company SOPs and product registrations are followed and maintained. Conducts investigations of batches, preps, lots, equipment, and facilities in accordance with the Code of Federal Regulations. Assists the Operations and Quality Operations departments in satisfying all FDA and DEA requirements.

 

What will you do

Investigates deviations to identify the probable root cause of the incident and corrective actions.Determines if batch is acceptable to release, or to deny release, what corrective actions are necessary and provide follow-up to ensure that corrective actions have been implemented.Assures review of incident by appropriate level of management and must notify management of serious incidents that require management’s review and action.Conducts GMP inspections of facilities to assure compliance with the current GMP regulations.Performs housekeeping inspections to assure Operations is maintaining work areas in an orderly and clean manner.Conducts cleaning inspections of equipment and areas.Recommends changes to batch records for clarification and compliance. Assures that operators are following written instructions and methods.
How will you get here?

Education:

Bachelors Degree in Chemistry, Biology, Engineering or relevant science preferred.

 

Experience:

Minimum of 3 years experience in Records, QC, QA, Analytical Development, Process Engineering, Engineering services or manufacturing

 

Equivalency:

Equivalent combinations of education, training, and related work experience may be considered.

 

Knowledge, Skills, Abilities

Requires extensive understanding of the practices, principles and theory of GMP ServicesMust be able to identify and analyze unique problems.Excellent problem solving and writing skillsStrong Proficiency in Microsoft Office SuitesAbility to work on multiple projects simultaneouslyStrong attention to detailTechnical writing knowledgeRoot cause analysis experience.