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    Specialist, Process Technician - Leiden, Nederland - Bristol Myers Squibb

    Bristol Myers Squibb
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    OTHER
    Beschrijving
    Working with Us
    Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

    Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: .

    Position Summary

    The Specialist Process Technician is responsible for performing/providing maintenance, installation, and troubleshooting of GMP process equipment used in manufacturing, warehouse and analytical labs at the production site. All work to be completed safely and to assure minimal impact to production while complying with cGMPs.

    Key Responsibilities
    • Execute routine to intermediate level maintenance activities and operate plant clean utility and process & lab equipment to sustain a cell therapy biopharmaceutical manufacturing facility in accordance with CFRs, SOPs, job plans, and BMS policies.
    • Assures that all documentation is stored in CMMS and Document Management Systems compliant to GxP regulations.
    • Participates in a detailed training program, to develop one's knowledge in the maintenance and operations field, as well as other areas of the facility.
    • Assists in review related SOPs or job plans/work plans for work related areas.
    • Provides basic troubleshooting of clean utilities and process & lab equipment/systems.
    • Requires on-call duty and if needed overtime and weekend hours. Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations.
    • Contact with F&E Team, Manufacturing, Warehouse & Lab Operators and Vendors.
    • Will have daily contact with her/his supervisory staff for work assignments and coaching.
    Qualifications & Experience

    Education
    • Requires at least a MBO level 4 diploma, technical degree preferred and/or equivalent experience in maintenance, or related technical discipline
    • Proficiency in reading and writing English
    Experience
    • 3+ years of experience in maintenance, preferably related to process-,lab equipment and clean utilities.
    • Direct experience working in GMP facilities, including understanding of GMP record keeping and documentation practices.
    • Proven expertise in troubleshooting and repair of electro-mechanical systems and instrumental equipment.
    • Ability to work in a later stage in 24/7 operation shift.
    • Attention to detail and follow-through.
    • Unwavering commitment to implement and follow safety protocols and work practices.
    • Experience in working with Computerized Maintenance Management Systems
    • Self-motivated, pro-active, and able to work with minimal supervision.
    • Excellent written and verbal communication skills in English
    Working Conditions

    Basic lifting involved, accessing large manufacturing equipment, gowning for clean/controlled areas, exposure to chemicals, access to secured areas, exposure to confined space, ability to work at different heights.

    #BMSCART

    #LI-Onsite

    If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

    Uniquely Interesting Work, Life-changing Careers
    With a single vision as inspiring as Transforming patients' lives through scienceTM , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

    On-site Protocol
    Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

    BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

    BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

    BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

    Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


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