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USP Manufacturing Specialist

Thermo Fisher Scientific

USP Manufacturing Specialist

full-timePosted: Aug 28, 2026Updated: Sep 1, 2026Switzerland, Lengnau

Job Description

Work ScheduleRotational days/weekendsEnvironmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, 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.)Job DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.Location/Division Specific Information:Lengnau BE, SwitzerlandHow Will You Make an Impact?:As an Upstream Manufacturing Specialist, you conduct the production of recombinant products by operating automated production equipment and support project teams in the design, commissioning, qualification and validation of new production lines for recombinant products.Responsibilities:Support operational readiness for Upstream Processing and cleaning.Participates in Technology Transfer of new products. Supports CVQ, PQ, Process Validation executionResponsible for the day-to-day execution of manufacturing activities in Upstream processing.Owns Work Instructions and SOP in their areaSupport Manufacturing Excellence to run robustly and efficiently.Participates in defining robust process parameters during routine manufacturing campaignsParticipate in New Product Introduction activitiesQualifications and Experience:Degree in pharmaceutical, food or chemistry1-3 years successful experience in pharmaceuticals operations in a GMP relevant environmentExperience in pharmaceutical industryWillingness to learnCan-do attitudeHands on mentalityShift work is expectedOn-call duties is expectedWhat We Offer:CompensationCompetitive PayPerformance Related Bonus where eligibleAnnual merit performance-based increaseExcellent BenefitsMedical benefitsPaid Time Off/Annual LeaveEmployee Referral BonusCareer Advancement Opportunities

Locations

  • Switzerland, Lengnau

Skills Required

  • pharmaceuticals operations in a GMP relevant environmentintermediate
  • pharmaceutical industryintermediate

Required Qualifications

  • Degree in pharmaceutical, food or chemistry (degree in pharmaceutical)
  • 1-3 years successful experience in pharmaceuticals operations in a GMP relevant environment (experience, 3 years)
  • Experience in pharmaceutical industry (experience)
  • Willingness to learn (experience)
  • Can-do attitude (experience)
  • Hands on mentality (experience)
  • Shift work is expected (experience)
  • On-call duties is expected (experience)
  • Degree in pharmaceutical, food or chemistry (degree in pharmaceutical)
  • 1-3 years successful experience in pharmaceuticals operations in a GMP relevant environment (experience, 3 years)
  • Experience in pharmaceutical industry (experience)
  • Willingness to learn (experience)
  • Hands on mentality (experience)
  • Shift work is expected (experience)

Responsibilities

  • Support operational readiness for Upstream Processing and cleaning.
  • Participates in Technology Transfer of new products. Supports CVQ, PQ, Process Validation execution
  • Responsible for the day-to-day execution of manufacturing activities in Upstream processing.
  • Owns Work Instructions and SOP in their area
  • Support Manufacturing Excellence to run robustly and efficiently.
  • Participates in defining robust process parameters during routine manufacturing campaigns
  • Participate in New Product Introduction activities
  • Support operational readiness for Upstream Processing and cleaning.
  • Participates in Technology Transfer of new products. Supports CVQ, PQ, Process Validation execution
  • Responsible for the day-to-day execution of manufacturing activities in Upstream processing.
  • Owns Work Instructions and SOP in their area
  • Support Manufacturing Excellence to run robustly and efficiently.
  • Participates in defining robust process parameters during routine manufacturing campaigns
  • Participate in New Product Introduction activities
  • What We Offer:CompensationCompetitive PayPerformance Related Bonus where eligibleAnnual merit performance-based increaseExcellent BenefitsMedical benefitsPaid Time Off/Annual LeaveEmployee Referral BonusCareer Advancement Opportunities

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