Quality Control Analyst Chemistry
vor 1 Woche
Quality Control Analyst Chemistry
Apply locations Boudry time type Full time posted on Posted 2 Days Ago job requisition id R1587685
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.
This position is responsible for performing all types of analytical testing required for the release of raw and packaging materials, final product, and stability samples, as well as all IPC testing. Additional responsibilities can include support of stability studies, handling of deviations, and change controls.
As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory.
He/she carries out activities in compliance with laboratory procedures and safety rules (EHS), as well as good documentation and good manufacturing practices (GDP and GMP).
Duties/Responsibilities
- Perform analytical testing (HPLC, GC, UV/VIS, dissolution, pH, titration, weighing) and peer review of testing raw data, paying strong attention to details and in accordance with applicable procedures and cGMP requirements.
- Perform review of analytical data.
- Perform basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs, etc.).
- Write specific standard operating procedures (e.g., operation and maintenance of equipment).
- Handle deviations and participate as SME when required.
- Can be assigned special tasks and projects according to the Company’s needs.
- Perform other tasks as assigned.
- Respect applicable EHS rules and propose improvements to EHS processes in the lab.
- Act as a SME and share expertise with colleagues regarding methods, equipment, and QC processes.
- Train peers on new activities and new hires.
- Create and update technical documents, such as procedures and work instructions.
Qualifications
Specific Knowledge, Skills, Abilities:
- Education/Experience/Licenses/Certifications: Federal Certificate of Capacity as Laboratory Technician or similar education; 2 – 3 years of work experience in a GMP environment.
- Advanced hands-on experience with analytical chemistry testing.
- Excellent knowledge in analytical chemistry techniques, instruments (HPLC/UPLC, GC, dissolution), and CDS.
- Experience of doing analytical testing according to Ph. Eur. and USP prescriptions.
- Strong attention to detail.
- Ability to work under limited supervision for extended periods of time.
- Good knowledge of laboratory safety rules.
- Ability to accurately and completely understand, follow, interpret, and apply Global Regulatory and cGMP requirements: uses good judgment and follows procedures.
- Capable of independent problem-solving; informs management as appropriate.
- Ability to write business and technical documents (good technical writing skills).
- Ability to communicate effectively with peers (QC members, management, other departments).
- Good knowledge of the LEAN and 5S concepts and methodologies.
- Good knowledge in English and French.
- Good knowledge of most common office software and capability of handling more complex lab software (e.g., Empower, LIMS).
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science,” 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 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.
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.
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