Clinical Packaging Operator Technician

Bristol-Myers Squibb; New Brunswick (NJ); On-site; USD 48,000 - 68,000; Full time

Job summary

Bristol Myers Squibb is seeking a Clinical Packaging Operator Technician for the New Brunswick site. This hourly union-backed role involves packaging clinical supplies, labeling, capping, and preparing vials and containers for studies under GMP conditions.

The position requires an associates degree or equivalent, or four years CGMP‑regulated experience in lieu of the degree, and proficiency with SAP. Work is conducted in a collaborative, safety‑driven environment with strict quality controls.

Qualifications

• Two year Associates degree or equivalent.
• In lieu of a two‑year degree, a minimum four years applicable experience within a CGMP regulated industry will meet requirements.
• Proficiency in the use of computer programs/systems is essential.

Responsibilities

• In accordance with specific instructions, performs a variety of functions involved in the preparation of packaged clinical supplies, including filling, labeling, capping, and sealing containers.
• Uses equipment to assemble products/devices for use in clinical studies.
• Performs in‑process sampling and records data obtained during operations.
• Inspects labels against proofs and documentation for count, text, and cosmetic defects.
• Completes documentation and interfaces with SAP and data collection systems; ensures label/accountability calculations are accurate.

Skills

Attention to detail

Computer literacy

Education

Two year Associates degree or equivalent

Four years CGMP experience in lieu of degree

Tools

SAP

Job description

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.

HOURLY UNION POSITION — This position is represented by the United Steelworkers (USW) Local #4-438

Permanent Position – Clinical Packaging Technician – 25 Shift: 7:00 am - 3:30 pm Site: New Brunswick Bldg: 107 Rate: $42.04

Non-Excluded Classification Description The goal of Product Development within Global Product Supply (GPS) is to develop new drug candidates and the processes to manufacture them into commercial realities. This is achieved by designing and conducting a variety of experimental studies using the latest scientific methods and state of the art equipment and instrumentation. The development process is very dynamic, with performance in both laboratory and process scale-up facilities. Scientific rigor, timeliness, and compliance with all GMP and federal/state/local regulations are a necessity. In order for the development process to be successful, there must be excellent collaboration between the professional and union staffs. Often, the professional staff will need to take a hands‑on approach during the course of an experiment as necessary, based on sound scientific judgment. Involvement of the union staff in the various experimental studies and other processes is determined by the professional staff on a case‑by‑case basis, because of the non‑routine, dynamic nature of the development process. Daily assignments will be based on demonstrated technical competence of the individual operator and the demands of the process. Priorities will be set based on the needs of the business. Both written procedures and verbal instructions by a supervisor will be executed with strict attention to safety and quality. Accurate and timely execution and documentation of activities and results are a requirement. Strict adherence to GMP, federal, state, and local regulations is required. Collaborative work with other employees is a necessity to achieve departmental and company goals.

Education Requirements

• Two year Associates degree or equivalent.
• In lieu of a two‑year degree, a minimum four years applicable experience within a CGMP regulated industry will meet requirements.
• Proficiency in the use of computer programs/systems is essential.

Technicians must maintain their skills and knowledge current with the advances in the field of Pharmaceutical Development. Incumbents may attend internal or external training courses as approved by management. Training will be implemented to ensure operators receive relevant training to facilitate the performance of their job responsibilities. Assessment after training specific to a task will be an ongoing requirement. Interactive training modules may be used for training on specific competencies. If testing is not passed, the interactive learning and testing will be repeated.

Working Conditions

Works under direction of supervision and follows established practices in performing all duties. Makes a decision when general instructions, established methods, or clearly defined precedents indicate action to be taken, but refers unusual problems to supervisors. Department requires zero error rate and employs multiple redundant checks to achieve this objective. Undetected errors may have serious implications and may result in costly withdrawals or the termination of a clinical study. Work is routine and repetitive, requiring application of judgement within limitations established by CGMP regulations, defined SOP's, and processing instructions. Required to document operations in exacting fashion without error. Requires interface with computer‑based documents and instructions such as but not limited to SAP. As required, handling of potent compounds requires annual gown/respirator training and medical respirator clearance. Work environment may be subject to odors and fumes, dust, powders, oil, grease, and noise. Significant physical effort is required. It is essential that incumbents be involved in stooping, lifting, and bending, sometimes in awkward positions. Employees must have annual eye exams and be able to qualify as required to perform Visual Inspection of Parenteral Products (i.e., liquid filled and lyophilized vials and syringes). This requires individuals to pass biennial re‑qualification.

Job Function — Clinical Supply Operations Packaging and Labeling

In accordance with specific instructions, performs a variety of functions involved in the preparation of packaged clinical supplies, including: Filling, labeling, capping, and sealing a variety of vials, bottles, unit dose blister cards, pouches, or other containers prepared for use in clinical studies, clinical stability, or product registration use. Using equipment, assembles combination products/devices to be used in clinical studies. Performs in‑process sampling during operations and records data obtained. Weighs and/or hand counts dosage forms and records data obtained within the appropriate documents. Inspects labels (manually and with use of electromechanical equipment) against label proofs and other supporting documentation for confirmation of, but not limited to, the following characteristics: count, variable text, character verification, and cosmetic defects. Label inspection must be accurate with no room for deviations. Completes all documentation supporting the preparation of clinical supplies and label inspection through interface with software‑based processing instructions and data collection systems, and use of equipment PLC's. Performs product inspection of supplies using SAP interface or other electromechanical equipment for verifying contents. Through interface with SAP, performs calculations of label and product accountabilities. Alerts supervision of any irregularities in procedures or equipment operations. Makes up carriers and shippers and prepares finished supplies for shipment. Assists in the (re)qualification and (re)validation of processing equipment. As necessary, cleans and wipes ceilings, floors, and walls in the prescribed manner. Performs, as required, Visual Inspection of Parenteral Products (i.e., liquid filled and lyophilized vials and syringes). This requires the operation of the semi‑automated vial inspection machine or the use of manual inspection booths. Individuals must pass inspection qualification and biennial re‑qualification, including annual eye exams. Completes all documentation supporting the inspection of parenteral supplies through interface with software‑based processing instructions. Performs other duties of equal or lesser nature as required, such as but not limited to: movement of material between work locations, organizing CSO warehouse, and general housekeeping. Follows Current Good Manufacturing Practices, departmental SOP's, good housekeeping principles, and all safety rules. Interfaces with computer‑based applications for self‑paced online training of both company and departmental policies and procedures. Follows Current Good Manufacturing Practices, all safety rules and good housekeeping principles.

Compensation Overview

The pay range for this position at commencement of employment is expected to be $42.04 per hour. The Clinical Packaging Operator Technician position will be covered by the collective bargaining agreement between Bristol Myers Squibb and the United Steel, Paper and Forestry, Rubber, Manufacturing, Energy, Allied Industrial and Service Workers International Union (USW) and its Local 4-438. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial wellbeing resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.

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. For roles based in Los Angeles County only: 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/

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] with 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.

R1606005 : Clinical Packaging Operator Technician Data Privacy Link

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.