Job Description

Work Schedule

Standard (Mon-Fri)

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, Laboratory Setting, Loud Noises (Equipment/Machinery), 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.), Standing for full shift, Will work with hazardous/toxic materials

General Summary:

Join Thermo Fisher Scientific Inc. as a Manufacturing Sciences Supervisor, influencing advancements and upholding quality.

Essential Functions:

• Lead and assist a team of scientists and technicians to complete operations successfully and in a timely manner.
• Lead root cause analysis and implement corrective actions.
• Train scientists in standard methodologies, assess inquiries, and lead complex problem-solving initiatives.
• Engage in PPI/Kaizen processes to drive continuous improvement.
• Balance multiple internal and external programs independently.
• Review protocols and documents to ensure accuracy and compliance.
• Generate and manage program timelines and schedules.
• Develop a deep understanding of all equipment and operational processes.

Physical and Environmental Requirements:

• Complete gowning certification for powder manufacturing.
• Wear Personal Protective Equipment (PPE) as needed.
• Lift up to 25 pounds repetitively, and up to 65 pounds non-repetitively.
• Adapt to critical and shifting timelines with a positive attitude.
• Work overtime and nonstandard schedules as needed to meet production demands.
• Handle biologic substances safely.
• Adjust to changing working conditions and physical requirements as necessary.

Essential Knowledge, Skills & Experience:

• Bachelor's degree in chemical engineering, biochemistry, biology, or a related field with 3-4 years of experience.
• Over 3 years of experience in the GMP regulated Biologics/Pharma industry.
• Proven leadership in managing clients, projects, and training associates.
• Strong understanding of current Good Manufacturing Practices (cGMP) requirements.
• Proficiency in technical writing, including Manufacturing Batch Records, Validation Protocols, and Technical Reports.
• Advanced knowledge in a specialty or expert cross-disciplinary knowledge of process development.
• Proactive in identifying and driving engineering initiatives for continuous improvement.
• Outstanding problem-solving skills to address deviations and implement corrective actions.
• Excellent interpersonal skills for successful collaboration across departments.
• Basic understanding of regulatory requirements (FDA/USP/EP).

By joining our team, you will be part of a world-class organization that values integrity, intensity, innovation, and involvement. We are committed to making a positive impact on the world through our outstanding products and services. Apply today and help us achieve our ambitious goals!

Job Tags

Remote job, Full time, Work at office, Shift work,

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