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: Senior Parenteral Manufacturing Technician

Location: Manati

1. Perform mechanical evaluation and troubleshooting

• Performs initial evaluation and minor troubleshooting diagnosis of manufacturing equipment failures
• Supports maintenance personnel in major troubleshooting diagnosis activities.

2. Performs complex and highly technical manufacturing operations of aseptic processing and/or isolator technology such as Diafiltration and Concentration of Proteins, Formulation of Proteins, Filling of Proteins in syringes and Vials within Isolators / Barrier Systems or in aseptic area process, Lyophilization process with Automatic Loading within Isolators / Barrier Systems or loading Lyophilizers on aseptic environment, Clean in Place (CIP) and Steam in Place (SIP) process in different systems, Decontamination of Isolator/ Barrier System with Vapor Hydrogen Peroxide (VHP), Sterilization cycles with Steam Autoclaves and Dry Heat Ovens and Tunnels, Isolators and gloves leak test.

• Operates in an efficient manner of the manufacturing processes to maximize product yield of products.
• Monitors critical process parameters and proactively takes necessary action to prevent process deviation and/or product losses.
• Maintains housekeeping within controls and aseptic environments, according to procedures.
• Handle Hazardous and Non hazardous waste according to EHS procedures.
• Receives, verifies and maintains all production records and transaction documents error free and in compliance with established procedures including computer generate transactions.
• Receives, handle, verifies and weights excipients, drug substances, and/or active ingredients.
• Performs systems integrity test such as isolators, ultra filtration skid, distribution systems, filters and gloves as required.
• Verify calibration status of critical instruments before process operation.
• Complete production documentation legible, error free and on time following good documentation practices.

3. Performs other duties to support other functional areas such as:

• Assist manufacturing activities in other areas within operations as required.
• Initiates, participates, and assists in resolution of quality investigations.
• Audits batch records and documentation, as required.
• Revises and improves procedures and develops new SOPs based on observations and experiences.
• Participates in special projects, during audits and regulatory inspections as required.
• Participates and assists in area validation and qualification activities.
• Supports the Annual Requalification Program by assuring plan execution on established timeframe

4. Attends to all mandatory training meetings for cGMP’s, EHS and Company Policies.

• Associate degree in a technical field with seven (7) years of experience in the pharmaceutical field or, Bachelor Degree with five (5) years experience in a Parenteral Manufacturing /Finishing in the Pharmaceutical Industry or Isolation technology.
• Basic writing skills when completing area documentation.
• Ability to troubleshoot equipment problems and provide resolutions using appropriate problem solving methodology.
• Basic knowledge on Computerized, PLC control equipment, procedures and new scientific processes and how to troubleshoot them.
• Ability to work with minimum supervision.
• Ability to provide job training, theoretical and/or On the Job, for new employees following the Parenteral Operations Department Qualification Curriculum.
• Knowledge on critical process parameters and their impact in product quality.
• Knowledge in steam sterilization, depyrogenation, filtration sterilization, lyophilization and isolators technology.
• Understanding of Process Equipment set-up and able to perform it repeatedly and according to SOPs.
• Ability to apply critical thinking to resolve complex issues and day-to-day situations.
• Excellent leadership characteristics, accountability and commitment.
• Ability to read, write, comprehend detailed technical information and directions and read procedures and documents in English/Spanish Text (e.g. SOPs, Batch Records, etc.)
• Team player and collaborating skills.
• Knowledgeable in cGMP’s, process area, documentation, safety, EHS and hygiene practices.
• Functional and basic technical knowledge of complex and automated equipment (computer, or PLC control) for set-up, operation and troubleshoot using the interface systems.
• Skill in performing detailed tasks and documenting information.
• Ability to enter data into a computer and perform complex process transactions.
• Skill in accurate visual inspection (e.g. product and components defects)
• Skill in basic mathematical applications.
• Skill in navigating through and performing transactions in mfg computer systems (HMI, hand held computers).
• Ability to relate and convert from metric (S.I.) to/from English units.
• Ability to plan and/or follows work schedules, set priorities
• Strong organizational skills
• Able to wear sterile gowns, mask, and full face respirators and able to use Full Face Mask, Latex/Nitrile Gloves, and disposable uniforms on a daily basis.
• Willing to work irregular hours, rotative shifts, weekends and holidays when necessary
• Ability to operate pallet jacks

BMSBL

#LI-Remote

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
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.

COVID-19 Information
To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

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

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.