Jobs

    Manager, Senior Engineer I - Boudry, Schweiz - Bristol Myers Squibb

    Bristol Myers Squibb
    Bristol Myers Squibb Boudry, Schweiz

    vor 3 Wochen

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    Ganztags
    Beschreibung
    Working with Us
    Challenging. Meaningful. Life-changing. Words you don't usually hear in the job world. But at Bristol Myers Squibb, it's anything but your typical job. Here, interesting work happens daily across all departments. From optimizing production lines to groundbreaking advancements in cell therapy, the work we do here truly makes a difference in patients' lives and the careers of those involved. You'll have the opportunity to grow and excel through unique and extensive opportunities, working with diverse and high-achieving teams. Take your career to new heights beyond your expectations.
    Title: Manager, Senior Engineer I
    Location: Boudry, Switzerland
    At Bristol Myers Squibb, we are revolutionizing the future of Cell Therapy. With our ambitious goals, industry-leading team, and long-term dedication, we are at the forefront of unlocking the full potential of Cell Therapy to bring hope to more patients. If you're ready to challenge yourself, advance your career, and inspire new hope in patients, there's no better place than here at BMS with our Cell Therapy team.
    The role of Manager, Senior Engineer I involves supporting the production of personalized cell therapy products at Contract Manufacturing Organizations (CMOs) for global clinical trials and commercial supply, working closely with the US-based External Manufacturing GMSAT team.
    Potential responsibilities include:
    • Functioning as technology and process Subject Matter Expert (SME)
    • Providing real-time troubleshooting and technical process support for ongoing manufacturing activities
    • Leading deviation investigations and identifying Corrective and Preventative Actions (CAPAs)
    • Approving manufacturing batch records, change controls, and deviations
    • Implementing process changes and improvements
    • Ensuring process control through data monitoring
    • Supporting technology transfer and process changes
    • Collaborating with various teams and stakeholders
    Qualifications & Experience:
    • Bachelor's Degree in science or engineering
    • Eight or more years of experience in biopharmaceutical manufacturing support
    • Expertise in SOPs, cGMPs, and regulatory environments
    • Preferred experience in Lean Six Sigma, Cellular therapies, and process validation
    • Ability to work effectively in cross-functional teams
    • Knowledge of cGMPs and biopharmaceutical regulations
    • Strong problem-solving skills
    • Experience with single-use technologies and cold chain/cryogenic technologies
    Uniquely Interesting Work, Life-changing Careers
    With a vision as impactful as "Transforming patients' lives through scienceTM", every BMS employee contributes significantly to work that surpasses the ordinary. Empowered to utilize individual talents in an inclusive culture, we promote diversity in clinical trials, fostering our values of passion, innovation, urgency, accountability, inclusion, and integrity to unleash the full potential of our team.
    On-site Protocol
    BMS has a varied occupancy structure that defines work requirements. Site-essential roles mandate full onsite shifts, while site-by-design roles may have a hybrid model. Field-based and remote-by-design roles necessitate physical travel for essential job functions.
    BMS prioritizes the well-being of employees and communities, strongly recommending full vaccination for Covid-19 and keeping up with boosters. The Company welcomes applicants with arrest and conviction records and ensures data privacy compliance with all applicable regulations.


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