Job Title: Lead QC Sample Management Technician

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Location/Division Specific Information

St. Louis, MO

How will you make an impact?

for performing a variety of duties to support Quality Control- Sample Management. Responsibilities of Sample Management include chain of custody, dispensing to laboratories, preventative maintenance, shipping samples to sites as applicable, and aliquoting from bulk material. This person is responsible for drafting procedures, participating in special projects, and performing more elaborate functions as required.

What will you do?

• Independently prepare for and BOTS, work instructions, and/or SOPs, with focus on “on time delivery” and "right the first time" executions
• Documentation of all activities to meet cGMP/cGDP requirements. Maintain compliance in assigned work and follow all safety procedures, to include the use of Person Protective Equipment.
• Perform and complete area assigned PMs as requested.
• Participate in cross-functional activities.
• Properly document activities per GMP procedures.
• Maintain up to date training records.
• Assist in training technicians.
• Schedule activities and coordinate the shift huddle in absence of the supervisor.
• Participate in cross-functional teams to complete projects.
• Participate in 1-1’s, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities).
• Lead team meetings and daily huddles for team as required. Act as liaison with other groups within the QC / manufacturing organization and a Subject Matter Expert for QC Sample Management.

How will you get here?

• Minimum one (1) year of college in a Science or Engineering related field (Biology, Biochemistry or Chemistry preferred)

• 2+ years of related experience in biopharmaceutical or pharmaceutical industry preferred

• 2+ years of experience in a cGMP laboratory preferred

Knowledge, Skills, Abilities

Knowledge

• Working knowledge of GMP regulations in a GMP environment
• Knowledge of cGMP practices and aseptic techniques

Skills

• Analytical Skills
• MS Office
• Strong math skills
• Strong prioritization skills
• Detail oriented
• Results driven
• Safety Mindset

Abilities

• Able to read, write, and communicate in English
• Able to understand and carry out instructions
• Reliable
• Strong communication (written and verbal)
• Effectively multi-task
• Able to work in an environment of change
• Able to work independently and as part of a team
• Able to recognize problems developing, not just occurring
• Occasional heavy lifting or moving required

At Thermo Fisher Scientific, each one of our 65,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.