Pharmaceutical Development Technician, Clinical Supply Planning & Operations at Bristol-Myers Squibb

New Brunswick, New Jersey, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

Ability to work with chemical, radiological, or biological agents that may be hazardous to health if mishandled (including agents that may potentially affect reproduction or the fetus)
Follow all safety procedures and use personal protective clothing/equipment where specified
Demonstrated technical competence for daily assignments
Strict adherence to cGLP/GMP, federal, state, and local regulations
Accurate and timely execution and documentation of activities and results
Ability to follow both written procedures and verbal instructions from a supervisor with strict attention to safety and quality
Collaborative work with other employees to achieve departmental and company goals
Availability for 7 AM - 3:30 PM EST shift at NBR Bldg #105/109

Responsibilities

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 forklifts
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, dispensing areas, and related equipment
Design and conduct experimental studies using scientific methods and state-of-the-art equipment in laboratory and process scale-up facilities
Execute daily assignments based on process demands, with scientific rigor and timeliness

Skills

Pharmaceutical Development

Clinical Supply Planning

Supply Chain Operations

Laboratory Techniques

Safety Procedures

PPE

Chemical Handling

Biological Agents

Experimental Studies

Scientific Methods

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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