Qc Specialist, Laboratory Analyst

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 .

Position:QC Specialist, Laboratory Analyst

Location: Manatí PR

** Second shift 2:00-10:30 pm Sunday -Thursday or Tuesday to Saturday **

Key Responsibilities

1.Performs testing for raw materials, packaging components, intermediate products, finished products, and ILQ's as per currentmonograph/testing methods, USP, NF, proposed monograph or validation protocols (where applicable).
2.Processes and reports analyticaldata utilizing computer systems (e.g., Empower system, SAP, LIMS, etc.) and verifies data generated by otherpeers.
3.Evaluates and analyzes data to identify and understand quality performance trends.
4.Ensures the reliability of the analytical equipment and the integrity of the physical localities through the proper maintenance and housekeepingof the testing areas.
5.Performs laboratory equipmentdailycalibrations, verifications, qualification, validation, and troubleshooting.
6.Maintains accurate records of allwork performed and document testing results as per Good Documentation Practices and of alllaboratorynotebooks and worksheets as per QC SOP's.
7.Participates in process validation, laboratory equipmentqualification, and analytical method transfers.8.Recommends change to SOP's, protocols, monographs, etc.
9.Provides supporting the investigations of non-conforming results and resolution of investigations.
10.Assists in new laboratory personnel in training when required.
11.Follows laboratory SOPs for sample handlingand the proper management of data generated.
12.Participates in Company projects and programs, such as safety and environmental training, GMP's, SOP's and others as required.
13.Purchases and maintains inventory of required supplies (e.g., standards, reagents, etc.).
14.Conducts internal audits (e.g.,laboratory facilities,reference standard, reagents and product logbook audits, etc.).
15.Ensures thatuseapproved validated methods and specifications, to perform required testing when is involved in testing of finishedproducts,API's, biological drug substances, raw materials, intermediates / components and ensures all necessary testing is carried out.
16.Ensures that the Equipment that will use and that he/she are formally qualified before release testing of products/materials is performed.
17.Ensures that stability studiestestingfollow specific protocols and procedures.
18.Verifiesthat Laboratory procedures and specifications areconsistency with other site procedures and/or specifications and that are incompliance with BMS Policies and Guidelines.
19.Completes all required testing on time dictated by SAP and area cycle time requirements in compliance with company and regulatoryrequirements.

Qualifications & Experience
B.S. degree in Science with a major in Chemistry, Biochemistry,IndustrialChemistry, Biology or Medical Technology.
One (1) year of experience in a pharmaceutical environment.
Working knowledge of computer and appropriate software packages. (e.g., word processing, spreadsheets, Empower, communications like e-mail, LIMS, etc).
Knowledge on analytical data collection and documentation or other information (e.g. significant figures, rounding off rules, degradation products reporting, etc.)
Knowledge of laboratory equipment, such as: UV-Visible, FTIR, HPLC, GC, CE, Scanners, micro plate readers
Ability to perform basic troubleshooting, PM and/or calibration of laboratory equipment (column care and use, tools, in-line filters, etc.)
Ability to conduct a variety of analytical techniques-Knowledge of site safety, security, and environmental requirements (e.g. MSDS, safety inspection checklists, waste disposal, etc.)
In-depth knowledge in the use and interpretation of USP/NF
Basic knowledge and experience with QC SOP's, cGMP's, federal and other countries regulatory requirements, documentation procedures and company policies/procedures
Working knowledge of statistical techniques.
Ability to work in a teamwork environment.
Ability to plan work schedules and set priorities with urgency and meet deadlines within a complex, rapidly changing environment-Proficiency in oral and written communication skills in both, English and Spanish.
Willing to work irregular hours, rotation shifts, weekends and holidays, when necessary.

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.
#LI-Onsite
BMSBL

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 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 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 workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries ******. Visitcareers.bms.com/eeo-accessibilityto 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.