MBP Manufacturing Team Leader

MBP Manufacturing Team Leader

Lengnau Vollzeit Kein Homeoffice möglich
Dormont Manufacturing Co
Work Schedule
Rotational shift nights/weekends
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, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our mission is to enable our customers to make the world healthier, cleaner, and safer. Whether supporting life sciences research, solving complex analytical challenges, improving laboratory efficiency, or enabling the development and manufacture of life‑changing therapies, we are committed to delivering innovative solutions.
Our Lengnau site is a state‑of‑the‑art, multi‑purpose manufacturing facility designed for large‑scale biologics production, offering flexible technologies from development through to commercial manufacturing.
Position Summary As a Manufacturing Team Leader – Media & Buffer Preparation, you will be responsible for executing manufacturing activities related to media and buffer preparation, equipment preparation, and cleaning within a cGMP environment. You will operate automated production systems, ensure compliance with quality and safety standards, and support process optimization and new product introduction activities.
Key Responsibilities
Manage
operational readiness
for media and buffer preparation, equipment preparation, and cleaning activities
Execute
day-to-day manufacturing operations
in compliance with cGMP requirements
Operate and monitor
automated production equipment
Own and maintain
Work Instructions (WI) and SOPs
within your area
Support
Technology Transfer
activities and contribute to CVQ, PQ, and Process Validation execution
Participate in
New Product Introduction (NPI)
activities
Contribute to
Manufacturing Excellence initiatives
to ensure robust and efficient processes
Assist in defining and optimizing
process parameters
during routine manufacturing campaigns
Collaborate with cross‑functional teams (Quality, Engineering, Maintenance, PCS)
Ensure accurate
documentation and batch record completion
Qualifications & Requirements
Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Food Science, or related field
1–3 years of experience in pharmaceutical or biotechnology manufacturing in a
GMP environment
Strong understanding of
cGMP and quality compliance requirements
Hands‑on, proactive mindset with strong attention to detail
Experience with
automated systems and manufacturing equipment
is an advantage
Good knowledge of
documentation practices and batch record execution
Strong
problem‑solving and organizational skills
Ability to work effectively both independently and within a team
Good communication skills
Willingness to work
shift schedules and on‑call duties
Commitment to
safety and quality culture
What We Offer
Competitive compensation and annual incentive bonus
Comprehensive healthcare and employee benefits
Opportunities for career growth in a global organization
A dynamic and innovative work environment
A culture driven by
Integrity, Intensity, Innovation, and Involvement
Our Mission At Thermo Fisher Scientific, we are committed to enabling our customers to make the world healthier, cleaner, and safer. Join a team of over 100,000 colleagues working together to solve complex challenges and support patients in need.
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Dormont Manufacturing Co

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