MBP Manufacturing Professional

h3Work Schedule /h3pRotational shift nights/weekends /ph3Environmental Conditions /h3pAble 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.) /ph3Job Description /h3pThermo 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. /ph3Position Summary /h3pAs a Manufacturing Professional – 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. /ph3Key Responsibilities /h3ulliSupport operational readiness for media and buffer preparation, equipment preparation, and cleaning activities. /liliExecute day-to-day manufacturing operations in compliance with cGMP requirements. /liliOperate and monitor automated production equipment. /liliOwn and maintain Work Instructions (WI) and SOPs within your area. /liliSupport Technology Transfer activities and contribute to CVQ, PQ, and Process Validation execution. /liliParticipate in New Product Introduction (NPI) activities. /liliContribute to Manufacturing Excellence initiatives to ensure robust and efficient processes. /liliAssist in defining and optimizing process parameters during routine manufacturing campaigns. /liliCollaborate with cross-functional teams (Quality, Engineering, Maintenance, PCS) Ensure accurate documentation and batch record completion. /li /ulh3Qualifications Requirements /h3ulliDegree in Chemistry, Biochemistry, Pharmaceutical Sciences, Food Science, or related field. /lili1–3 years of experience in pharmaceutical or biotechnology manufacturing in a GMP environment. /liliStrong understanding of cGMP and quality compliance requirements. /liliHands-on, proactive mindset with strong attention to detail. /liliExperience with automated systems and manufacturing equipment is an advantage. /liliGood knowledge of documentation practices and batch record execution. /liliStrong problem-solving and organizational skills. /liliAbility to work effectively both independently and within a team. /liliGood communication skills. /liliWillingness to work shift schedules and on-call duties. /liliCommitment to safety and quality culture. /li /ulh3What We Offer /h3ulliCompetitive compensation and annual incentive bonus /liliComprehensive healthcare and employee benefits /liliOpportunities for career growth in a global organization /liliA dynamic and innovative work environment /liliA culture driven by Integrity, Intensity, Innovation, and Involvement /li /ulh3Our Mission /h3pAt 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. /p #J-18808-Ljbffr