PARENTERAL MANUFACTURING TECHNICIAN

Bristol Myers Squibb; Puerto Rico; Presencial; USD 23.000 - 28.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Time Off

11 paid holidays

Global Shutdown

Descripción de la vacante

Bristol Myers Squibb is seeking a Parenteral Manufacturing Technician to join our Manati, PR site. You will perform setup, cleaning, sterile processing, and line clearance according to approved SOPs, maintaining data integrity and supporting GMP compliance.

The role involves operation of filling equipment, CIP/SIP cycles, and in-process sampling within a fast-paced manufacturing environment. Responsibilities include inventory accuracy, batch record review, and collaboration with cross-functional

Formación

• Experience in aseptic manufacturing environments.
• Ability to follow SOPs and GDP.
• Strong attention to detail in repetitive tasks.

Responsabilidades

• Sets up, changes over, cleans, and performs line clearance per SOPs and safety procedures.
• Operates formulation, preparation, and filling equipment; performs basic troubleshooting.
• Cleans and sterilizes manufacturing areas and equipment per aseptic standards.
• Performs CIP and SIP operations for tanks and systems; conducts in-process sampling.

Conocimientos

Good Documentation Practices

Data integrity

Equipment operation

Descripción del empleo

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Schedule-5pm-5am- rotating days- dias rotativos

Execute Parenteral Manufacturing Operations

• Conducts equipment setup, changeover, cleaning, and line clearance following approved SOPs and safety procedures.
• Operates formulation, preparation, and filling equipment; performs basic troubleshooting and escalates abnormalities.
• Cleans, sanitizes, and sterilizes classified manufacturing areas and equipment in compliance with aseptic and contamination‑control standards.
• Operates autoclaves and executes sterilization cycles for manufacturing components and equipment.
• Performs Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) operations for tanks and systems.
• Executes pre‑ and post‑use filter integrity testing.
• Receives, verifies, handles, and weighs excipients and drug substances/active ingredients for formulation steps.
• Executes formulation processes per batch record instructions, including pH adjustment, yield calculations, mixing parameters, in‑process controls, and volume adjustments.
• Collects required in‑process samples following aseptic sampling techniques.
• Interacts with automated and computer‑controlled equipment, ensuring adherence to data integrity principles.

Documentation, Compliance, and Process Control

• Maintains accurate inventory of components and materials; submits timely requests to support uninterrupted operations.
• Completes all production records and system transactions accurately, legibly, and in real‑time following Good Documentation Practices (GDP).
• Verifies accuracy and completeness of manufacturing documentation, including computer‑generated transactions.
• Performs batch record audits, as required.
• Ensures assigned equipment is cleaned, labeled, calibrated, and qualified before use.
• Identifies opportunities to improve procedures and contributes to the development or revision of SOPs.

Execute Parenteral Manufacturing Operations

• Conducts equipment setup, changeover, cleaning, and line clearance following approved SOPs and safety procedures.
• Operates formulation, preparation, and filling equipment; performs basic troubleshooting and escalates abnormalities.
• Cleans, sanitizes, and sterilizes classified manufacturing areas and equipment in compliance with aseptic and contamination‑control standards.
• Operates autoclaves and executes sterilization cycles for manufacturing components and equipment.
• Performs Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) operations for tanks and systems.
• Executes pre‑ and post‑use filter integrity testing.
• Receives, verifies, handles, and weighs excipients and drug substances/active ingredients for formulation steps.
• Executes formulation processes per batch record instructions, including pH adjustment, yield calculations, mixing parameters, in‑process controls, and volume adjustments.
• Collects required in‑process samples following aseptic sampling techniques.
• Interacts with automated and computer‑controlled equipment, ensuring adherence to data integrity principles.

Documentation, Compliance, and Process Control

• Maintains accurate inventory of components and materials; submits timely requests to support uninterrupted operations.
• Completes all production records and system transactions accurately, legibly, and in real‑time following Good Documentation Practices (GDP).
• Verifies accuracy and completeness of manufacturing documentation, including computer‑generated transactions.
• Performs batch record audits, as required.
• Ensures assigned equipment is cleaned, labeled, calibrated, and qualified before use.
• Identifies opportunities to improve procedures and contributes to the development or revision of SOPs.

Support Manufacturing and Cross‑Functional Activities

• Initiates and participates in quality investigations, providing technical input and timely documentation.
• Supports onboarding and “on‑the‑job” training of new employees.
• Participates in internal, external, and regulatory inspections.
• Supports validation and qualification activities within the manufacturing area.
• Ensures timely execution of Environmental Monitoring sampling responsibilities.
• Supports annual requalification programs and area readiness activities.
• Provides assistance to other manufacturing areas as operational needs arise.
• Communicates status of documentation, activities, and pending actions to supervision and partner departments.

Ensure Safety, Environmental, and GMP Compliance

• Maintains housekeeping and aseptic conditions within controlled environments in alignment with contamination‑control practices.
• Handles hazardous and non‑hazardous waste according to Environmental, Health & Safety (EHS) procedures.
• Completes required training for cGMP, EHS, aseptic practices, and company policies.
• Actively identifies and reports safety risks, participating in initiatives to promote a safe and compliant work environment.
• Requires steady attention to detail during routine manufacturing tasks such as equipment setup, monitoring processes, and completing documentation.
• Must maintain awareness of process conditions, noticing alarms, unusual readings, or equipment irregularities and escalating them promptly.
• Requires regular use of digital systems and control screens, needing accurate visual checks and basic interpretation of displayed information.
• Must stay focused during repetitive tasks and when working inside controlled areas or around production equipment.
• Requires the ability to remain calm and attentive when unexpected situations arise, such as abnormal process conditions or minor deviations.
• Identify and promptly report inconsistencies, atypical conditions, or potential violations of company procedures, quality requirements, or safety policies to supervision.
• Plans and organize work activities with a sense of urgency, adjusting priorities to meet operational deadlines in a dynamic and rapidly changing manufacturing environment.
• Applies sound judgment to resolve routine operational issues, escalating when appropriate to ensure safe and compliant operations.
• Proposes alternatives and evaluates risks and benefits when supporting process decisions, aligning personal and team activities with departmental objectives, business priorities, and BMS values.

#BMSBL

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview

Manati - PR - US: $16.70 - $20.24per hour

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits

• Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).
• U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.
• Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.
• Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
• Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Years Day.
• U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People With Disabilities

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 [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1606231 : PARENTERAL MANUFACTURING TECHNICIAN