Senior Parenteral Manufacturing Technician

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Responsible for different parenteral manufacturing operations in addition to the mechanical, electronic diagnosis and troubleshooting involving highly sensitive pharmaceutical/biologics products equipment. This will include traditional aseptic process and/or Isolator Technology process. This position must comply with all Security Guidelines, Environmental Health and Safety regulations, SOP'S and the current Good Manufacturing Practices.


Perform mechanical evaluation and troubleshooting



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



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.



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



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


KNOWLEDGE/ EDUCATION/ EXPERIENCE:


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


CONCENTRATION AND VISUAL EFFORT:

The incumbent requires a special concentration in several operations activities such as : Working with Isolators, testing activities , weighing activities, equipment set up , troubleshooting, process calculations , gowning and aseptic techniques on aseptic environment, Lyophilization process, Formulation Process, etc. Demonstrates the attention of each process step on the whole operation. Understand and can explain process flow, sequence and his role and impact within the product manufacturing cycle.

INITIATIVE AND INGENUITY:

Plan and/or follows work schedules, set priorities with a sense of urgency and meet deadlines in a rapidly changing environment. Solve day-to-day situations that arise, generates alternatives and evaluates risk vs. benefits aligning personal, team and/or departmental activities with organizational goals and business strategies.

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 the resources to pursue their goals, both at work and in their personal lives.

Company: Bristol-Myers Squibb

Req Number: R1520951_EN

Updated: 2020-01-29 00:00:00.000 UTC

Location: Manati, PR

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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