Pharmaceutical Development Technician, CSO, Integrated Supply Chain & Regional Logistics

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.

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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.  Inquires for further information should be directed to the hiring manager.

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Temporary Position (6-month term) – Pharmaceutical Development Technician, Clinical Supply Logistics, Integrated Supply Chain & Regional Logistics – 25 – CSO

Shift: 7 AM - 3:30 PM EST      

Site: NBR

Bldg #109 (excluded)

Rate: $39.62 /hour

JOB FUNCTION:

PHARMACEUTICAL DEVELOPMENT TECHNICIAN – CLINICAL SUPPLY OPERATIONS – INTEGRATED SUPPLY CHAIN & 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.

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
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