Clinical Manufacturing Associate

Bristol Myers Squibb; New Jersey; On-site; USD 41,851 - 53,161; Full time

Job summary

A leading biopharmaceutical company in New Jersey seeks a Clinical Manufacturing Associate to produce blood component lots through various processes, including cell culture and cryopreservation. The role demands adherence to production schedules and recording of production data. Ideal candidates have a Bachelor's in a relevant science and experience in a cGMP/FDA-regulated industry. Competitive hourly pay is offered.

Qualifications

• Understanding of cell culture, cryopreservation, purification, and aseptic processing.
• Able to perform tasks in a cleanroom environment as per FDA regulations.

Responsibilities

• Produce blood component lots through various processes.
• Develop technical knowledge of assigned projects.
• Record production data clearly and concisely.

Skills

Basic understanding of cell culture

Experience within cGMP/FDA-regulated industry

Basic mathematical skills

Technical writing capability

Proficient in MS Office applications

Education

Bachelor’s degree in an applicable science

2 years relevant experience

Job description

Clinical Manufacturing Associate at Bristol Myers Squibb

Location: Warren, NJ (This role is 100% Onsite)

Pay: $30.38 - $38.59/hr on W2

Work Schedule: Friday- Tuesday, 8:30 AM-5 PM

Job Description

• Production of blood component lots through cell culture, harvest, and cryopreservation.
• Become fully trained and qualified in all aspects of assigned processes.
• Develop a high level of technical knowledge of project(s).
• Weigh and measure in-process materials to ensure proper quantities are added/removed.
• Adhere to the production schedule ensuring on-time internal production logistics.
• Record production data and information in a clear, concise format according to proper GDPs.
• Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
• Assist tech transfers in and out of the clinical facility.
• Motivated, team-conscious individuals are needed to fulfill job requirements.
• No direct reports will be assigned to this job role.
• Perform other tasks as assigned.

Desired Experience

• Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.
• Experience within cGMP/FDA-regulated industry.
• Basic mathematical skills.
• Technical writing capability.
• Proficient in MS Office applications.
• Background includes an understanding and application within industry of biology, chemistry, medical or clinical practices.

Ideal Candidates Would Also Have

• Advanced understanding of cell culture.

Other Qualifications

• Bachelor’s degree in an applicable science or 2 years relevant experience.

The starting hourly compensation for this assignment is within the range of $30.38 to $38.59/hr. Please note that the final individual compensation and any applicable benefits will be determined by your employer of record (and not the client). Factors influencing this decision may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location of the job. Compensation details are subject to change.