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Bristol Myers Squibb Technician, Metrology in Boudry, Switzerland

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: careers.bms.com/working-with-us .

The Technician, Metrology is responsible for executing, documenting, and overseeing calibration activities across departments, including Manufacturing, Quality Control, and Technical Services. This role ensures that all processes comply with cGxP standards and internal policies, safeguarding the accuracy and reliability of critical equipment. Beyond technical tasks, this position requires strong problem-solving skills to address calibration issues, assess risks, and propose solutions for diverse operational needs. Serving as a key collaborator, the Technician supports continuous audit readiness, drives quality initiatives, and promotes operational excellence. The Technician, Metrology is responsible for executing, documenting, and overseeing calibration activities across departments, including Manufacturing, Quality Control, and Technical Services. This role ensures that all processes comply with cGxP standards and internal policies, safeguarding the accuracy and reliability of critical equipment. Beyond technical tasks, this position requires strong problem-solving skills to address calibration issues, assess risks, and propose solutions for diverse operational needs. Serving as a key collaborator, the Technician supports continuous audit readiness, drives quality initiatives, and promotes operational excellence.

Duties/Responsibilities

  • Conduct routine and specialized calibration on a broad range of equipment and systems across the site, including Manufacturing, Quality Control, and Technical Services, ensuring accuracy and compliance with internal and external standards.

  • Maintain calibration records in line with equipment lifecycle requirements, including installation, modifications, and retirement of instruments.

  • Communicate the status of all instruments requiring calibration, ensuring all tags are current and accurately reflect calibration status.

  • Document calibration performed in calibration management software.

  • Adhere to all cGxP and EHS guidelines, maintaining records in compliance with Good Documentation Practices (GDP).

  • Review and validate calibration documentation, ensuring traceability and readiness for audits or inspections.

  • Develop and justify calibration procedures based on risk assessments and scientific rationales, enhancing accuracy and alignment with quality objectives.

  • Identify, investigate, and document any calibration-related deviations; coordinate corrective actions (CAPA) to resolve issues effectively.

  • Support cross-departmental troubleshooting efforts and collaborate on root cause analysis to drive preventive measures.

  • Collaborate with planning functions to ensure calibration activities are synchronized with operational requirements.

  • Oversee external vendors conducting calibration activities, ensuring adherence to internal standards and schedules.

  • Actively contribute to the development and continuous improvement of calibration and maintenance procedures, implementing best practices that meet GDP and GMP standards.

  • Actively engage in quality-related initiatives, participating in Change Control processes, quality risk assessments, and deviation investigations related to metrology.

  • Participate in continuous improvement efforts, proposing updates to calibration procedures or schedules based on data trends.

  • Provide support for project documentation review, ensuring metrology considerations are incorporated.

  • Ensure calibration activities align with the overarching quality management system and EHS objectives.

Qualifications

Formation Technical discipline (e.g. CFC polymechanics or equivalent with experience in quality / metrology domain)

Experience - Responsibility and minimum number of years.

  • 4+ years in Metrology function, preferably within the pharmaceutical or other GMP-regulated environment.

Competencies - Knowledge, Skills Abilities:

  • Knowledge of international cGxP regulations, GDP, and metrology principles.

  • Autonomous on a wide variety of equipment for calibration (Manufacturing, Quality Control, and Technical Services).

  • Proficient in using MS Office, calibration management systems, and asset management software.

  • Familiar with QA processes and compliance aspects.

  • Problem-solving aptitude, with the ability to autonomously handle routine and complex calibration tasks.

  • Strong player to collaborate in cross-functional teams, supporting a cohesive approach to equipment reliability and quality.

  • Ability to manage tight deadlines and handle multiple tasks simultaneously.

  • Good communication skills (French and English).

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 scienceā„¢ , 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

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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 adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

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

Company: Bristol-Myers Squibb

Req Number: R1587536

Updated: 2024-11-25 03:19:46.108 UTC

Location: Boudry-CH

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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