Job Description

Pharmaceutical Development Technician, Clinical Supply Planning & Operations Join to apply for the Pharmaceutical Development Technician, Clinical Supply Planning & Operations role at Bristol Myers Squibb . This is a 6‑month temporary, full‑time position based in New Brunswick, New Jersey (NBR). The rate is $40.81 per hour. 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 have the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. 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 at careers.bms.com/working-with-us . The following positions will require the employees to work with chemical, radiological, or biological agents that may be hazardous to health if mishandled (including agents which may potentially affect reproduction or the fetus). Employees will be required to follow all safety procedures and use personal protective clothing/equipment where specified. Inquiries for further information should be directed to the hiring manager. Job Function 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. Job Function – Clinical Supply Operations Integrated Supply Chain 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. Set up, 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 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. 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. Compensation & Benefits The pay range for this position at commencement of employment is expected to be $40.81 per hour, however, pay offered may vary depending on multiple individualized factors, including the employee’s work schedule, market location, job‑related knowledge, skills, and experience, as well as the terms of any applicable collective bargaining agreement. The position will be covered by the collective bargaining agreement between Bristol Myers Squibb and the Allied Industrial & Service Workers International Union. 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. Seniority Level Entry level Employment Type Full‑time Job Function Management and Manufacturing Industry Pharmaceutical Manufacturing Location South Brunswick, NJ We encourage you to apply even if your resume does not match all qualifications. You could be one step away from work that will transform your life and career. #J-18808-Ljbffr Bristol Myers Squibb

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