Job Information
Bristol Myers Squibb Mechanic, Inspection and Packaging Operations in Manati, Puerto Rico
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: Mechanic, OSD Operations Non Sterile
Location : Manati - PR
Saturday 6:00AM to 6:30PM and Sunday 6:00PM to 6:30AM plus 3 days weekdays 2:00PM to 10:30PM
OR Saturday 6:00PM to 6:30AM and Sunday 6:00AM to 6:30PM plus 3 days weekdays 2:00PM to 10:30PM
Key Responsibilities
Performs and documents preventive/predictive and corrective maintenance work orders according to schedule using current procedures for documentation to comply with cGMP's.
Performs Equipment Conditioned Based Monitoring, monitors critical process parameters and utilizes predictive technologies to proactively take the necessary action to prevent process deviation and/or product losses. Interacts with computer-controlled equipment and processes.
Complies with federal and local regulatory agencies (e.g., OSHA, EPA, FDA, DEA, etc.).
Works and operates hand tools, power tools, pneumatic tools, and accessories necessary to do general maintenance in an industrial manufacturing environment.
Keeps Microbiology, Inspection and Packaging equipment spare parts system up to date.
Supports the Microbiology, Inspection and Packaging technicians in the diagnostic troubleshooting of abnormal equipment operation.
Develops the maintenance plan (proactive, predictive, preventive, etc.) for existing and new operations equipment.
Recommends equipment upgrades to increase productivity in existing equipment and
Ensures equipment downtime is kept at a minimum level.
Assists in the FMEAs, RCAs (root cause analysis) and validation of equipment, as required.
Attends to all mandatory training meetings for cGMP's, EHS and Company Policies.
Revise, improve and develop new Job Plans based on observations, experience, and technical data. Complete work orders documentation legible, error free and on time following good documentation practices.
Participates in special projects and during audits and regulatory inspections as required
Qualifications & Experience
Associate Degree in Mechanical, Instrumentation, Electronics, Electricity or a Technical Degree in Instrumentation, Electronic, Electricity or Mechanic.
Five (5) years in a manufacturing pharmaceutical environment.
Basic writing skills when completing area documentation.
Ability to troubleshoot equipment problems and provide resolutions using the 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 Operations Department Qualification Curriculum.
Knowledge of all critical process parameters and their impact in product quality.
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.
Excellent leadership characteristics, accountability and commitment.
Ability to read, write, comprehend detailed technical information and directions.
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.
Ability to read procedures and documents in English/Spanish Text (e.g. SOPs, Batch Records, etc.)
Skill in basic mathematical applications.
Shifts
Saturday 6:00AM to 6:30PM and Sunday 6:00PM to 6:30AM plus 3 days weekdays 2:00PM to 10:30PM
OR Saturday 6:00PM to 6:30AM and Sunday 6:00AM to 6:30PM plus 3 days weekdays 2:00PM to 10:30PM
#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 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/ 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.
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: R1583284
Updated: 2024-07-18 05:08:18.203 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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