Pharmaceutical Development Technician, Cso - New Brunswick, United States - Bristol-Myers Squibb

Bristol-Myers Squibb

Verified Company

New Brunswick, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

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.
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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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Permanent Position - Pharmaceutical Development Technician, Integrated Supply Chain and Regional Logistics CSO

Shift:7 AM - 3:30 PM EST

Site:
New Brunswick, NJ

Bldg #109 (excluded)

Rate:
$38.47 / hour

JOB FUNCTION:

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 putaway 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 relabeling 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.

Company Union
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 wil