• Supervisor, Formulation Manufacturing - Nights

    ThermoFisher Scientific (St. Louis, MO)


    Work Schedule

    12 hr shift/nights

     

    Environmental Conditions

     

    Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Loud Noises (Equipment/Machinery), No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Will work with hazardous/toxic materials

    Job Description

    Downstream Processing Supervisor (Band 6)

    **Location:** St. Louis, MO | Drug Substance Division (Biologics)

    **Work Schedule:** Nights, 12-hour shifts (2, 2, 3 rotation)

    **Shift Differential:** 15%

    Discover Impactful Work:

    Join Thermo Fisher Scientific as a Downstream Processing Supervisor and play a pivotal role in the success and oversight of downstream manufacturing processes. Be responsible for conducting a variety of functions related to Downstream Biopharmaceutical Manufacturing, including large scale chromatography, viral inactivation, viral filtration, ultrafiltration, diafiltration, and aseptic filling of bulk drug substances.

     

    Explore an outstanding chance as a Supervisor in Formulation Manufacturing - Nights with Thermo Fisher Scientific Inc. Join our team committed to excellence and teamwork.

    Responsibilities

    + Supervise and lead night shift operations in the formulation manufacturing department, ensuring adherence to cGMP standards.

    + Coordinate flawless execution of manufacturing batch records, work instructions, and SOPs.

    + Strictly monitor and maintain suite, supplies, equipment, logbooks, and data integrity.

    + Proactively identify and resolve supply and raw material deficiencies, scheduling conflicts, and process deviations.

    + Conduct root cause analysis and drive continuous improvement initiatives.

    + Lead and facilitate daily huddles and shift exchanges, acting as a liaison and Subject Matter Expert.

    + Provide mentorship and training to team members, encouraging a collaborative and high-performance culture.

    + Ensure compliance with all safety regulations and promote safe work habits.

    Requirements

    + HS Diploma/GED required; Bachelor’s degree in Biology, Chemistry, Engineering, or related field preferred.

    + 5-9 years of relevant work experience, with at least 2 years in a supervisory role, preferably in the pharmaceutical industry.

    + Proven knowledge of cGMP practices, aseptic techniques, and chemical concepts.

    + Strong critical thinking, problem-solving capabilities, and effective communication skills.

    + Ability to multi-task, work independently, and collaborate within a team.

    + Physical capability to adhere to cleanroom gowning requirements and lift a minimum of 25 lbs independently.

    Keys to Success

    + Diligent and results-oriented with outstanding organizational skills.

    + Efficient in MS Office and capable of critical evaluation of processes.

    + Demonstrated ability to foster cross-functional relationships and improve team performance.

    + Dedication to maintaining a safe and compliant work environment.

     

    Join Thermo Fisher Scientific Inc. and contribute to making the world healthier, cleaner, and safer. Apply today and be part of our world-class team!

     

    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.