Pharmaceutical Development Technician - CSO CSPO

Bristol-Myers Squibb Company

New Brunswick (NJ)

On-site

USD 48,000 - 68,000

Full time

10 days ago

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Benefits offered by this job

Medical insurance
Wellbeing program
401(k)

Job summary

Bristol Myers Squibb in New Brunswick is seeking a permanent Pharmaceutical Development Technician to support clinical supply planning and operations within the regional logistics team. The role emphasizes adherence to cGLP/cGMP, data integrity, and safe handling of hazardous materials.

This union position offers a daytime shift and a site-based workplace. Applicants should have a two-year associate degree related to pharmaceutical development or operations, and be proficient with computer

Qualifications

  • Two year Associate Degree in Science related to Pharmaceutical Development or Business related to Operations/Supply Chain/Logistics or equivalent.
  • Proficiency in the use of computer programs/systems is essential.

Responsibilities

  • Weigh, dispense and label bulk drug substances, ingredients and packaging components for clinical programs.
  • Withdraw samples and transfer materials between buildings by hand trucks or fork lifts.
  • Set up, clean and operate areas and equipment in weighing/dispensing processes.
  • Record data per cGLP/cGMP regulations in paper and electronic formats.
  • Maintain warehouses and dispensaries in neat and safe conditions.
  • Pack and ship domestic and international shipments, including temperature-controlled items.

Skills

Attention to detail

Education

Associate Degree in Science related to Pharmaceutical Development/Operations/Supply Chain/Logistics

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.

Permanent Union Position - Pharmaceutical Development Technician - 25

Shift: 7:00 am-3:30 pm

Site: New Brunswick

Bldg: B105

Rate: $42.04

PHARMACEUTICAL DEVELOPMENT TECHNICIAN - CLINICAL SUPPLY PLANNING & OPERATIONS - REGIONAL LOGISTICS

The goal of Pharmaceutical Development within Research & Development (R&D) 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 performed in both laboratory and process scale-up facilities. Scientific rigor, timeliness and compliance with all cGLP/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 technician and the demands of the process. Priorities will be set based on the needs of the R&D 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 cGLP/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 Associate Degree in Science related to Pharmaceutical Development or Business related to Operations/Supply Chain/Logistics or equivalent. Proficiency in the use of computer programs/systems is essential. Technicians must maintain their skills and knowledge current with 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 PDT employees receive relevant training to facilitate the performance of their job responsibilities. Testing after training specific to an area will be an ongoing requirement. Interactive training modules will be used for training on specific competencies. If testing is not passed, the interactive learning and testing will be repeated. A pass/repeat summary of all testing on each module will be kept to assess the performance of the module.

WORKING CONDITIONS:

The position will require the employee to work with chemical, radiological and biological agents that may be hazardous to health if mishandled (including agents which may potentially affect development of the fetus). Assignments will be executed in laboratory, warehouse and process scale-up facilities interchangeably. The employee will be required to follow all safety procedures and use personal protective clothing/equipment as provided by the company where specified. Disagreeable conditions including odors, heat, noise etc. may be experienced.

JOB FUNCTION - CLINICAL SUPPLY OPERATIONS INTEGRATED SUPPLY CHAIN

Assignments within Integrated Supply Chain include, but are not limited to the following:

  • Weigh, dispense and accurately label bulk drug substances, ingredients, dosage forms, packaging components, and all materials needed to support clinical programs and product development
  • Withdraw samples from material containers, transfer materials between buildings and within buildings by means of hand trucks or fork lifts
  • Setup, clean and operate all areas and equipment required in the weighing and dispensing process
  • Record data as per cGLP and cGMP regulations in both paper and computer formats, per established procedures
  • Maintain the warehouse, dispensaries and other operations areas in neat and tidy conditions
  • Perform the receipt, reconciliation and put-away of inbound materials
  • Pack and ship both regular and temperature controlled, domestic as well as international shipments
JOB FUNCTION - CLINICAL SUPPLY OPERATIONS REGIONAL LOGISTICS

Assignments within Regional Logistics include, but are not limited to the following:

  • Perform the physical and system pick of finished clinical supplies for domestic and international shipments, ensuring the accuracy of the items picked to the container level
  • Pack finished clinical supplies for domestic and international shipments
  • Pack temperature controlled shipments to maintain temperature range specified for the product, according to the provided cold chain packing guidelines
  • Perform inventory/cycle counts of finished supplies within New Brunswick
  • Perform drug re-labeling activities and domestic and international shipment labeling
Compensation Overview:

The pay range for this position at commencement of employment is expected to be $42.04 per hour. The Pharmaceutical Development Technician - CSO CSPO 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 well-being 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 adastaffingsupport@bms.com. 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/

For roles based in Washington state only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

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.

R1607072 : Pharmaceutical Development Technician - CSO CSPO

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