Work Schedule
Rotational shift days
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
About Thermo Fisher Scientific
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 Professional –Upstream Processing, you will be responsible for executing manufacturing activities related to upstream processing 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
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Support operational readiness for media and buffer preparation, equipment preparation, and cleaning activities
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Execute day-to-day manufacturing operations in compliance with cGMP requirements
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Operate and monitor automated production equipment
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Own and maintain Work Instructions (WI) and SOPs within your area
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Support Technology Transfer activities and contribute to CVQ, PQ, and Process Validation execution
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Participate in New Product Introduction (NPI) activities
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Contribute to Manufacturing Excellence initiatives to ensure robust and efficient processes
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Assist in defining and optimizing process parameters during routine manufacturing campaigns
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Collaborate with cross-functional teams (Quality, Engineering, Maintenance, PCS)
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Ensure accurate documentation and batch record completion
Qualifications & Requirements
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Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Food Science, or related field
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1–3 years of experience in pharmaceutical or biotechnology manufacturing in a GMP environment
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Strong understanding of cGMP and quality compliance requirements
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Hands-on, proactive mindset with strong attention to detail
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Experience with automated systems and manufacturing equipment is an advantage
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Good knowledge of documentation practices and batch record execution
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Strong problem-solving and organizational skills
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Ability to work effectively both independently and within a team
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Good communication skills
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Willingness to work shift schedules and on-call duties
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Commitment to safety and quality culture
What We Offer
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Competitive compensation and annual incentive bonus
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Comprehensive healthcare and employee benefits
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Opportunities for career growth in a global organization
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A dynamic and innovative work environment
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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.
