Hands-On Upstream Manufacturing Associate

Pharma Universe; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Hands-On Upstream Manufacturing Associate to support cell culture operations in a cGMP environment. The ideal candidate will have extensive experience in upstream biologics manufacturing and a strong understanding of bioreactor operations. This full-time position offers relocation support for US citizens and is located onsite in New Jersey.

Benefits

Relocation support offered for US Citizens

Qualifications

• Minimum 3 years' experience in upstream biologics manufacturing in a cGMP environment.
• Proficiency in aseptic technique and working with single-use technologies.

Responsibilities

• Execute upstream manufacturing activities including cell culture and bioreactor operations.
• Support the production of engineering and clinical batches in compliance with cGMP standards.

Skills

Aseptic Technique

Attention to Detail

Documentation Skills

Education

Bachelor's or Master's degree in Biochemistry

Bachelor's or Master's degree in Chemical Engineering

Bachelor's or Master's degree in Biology

Tools

Bioreactor Operations

Single-Use Technologies

GMP Documentation

Job description

Hands-On Upstream Manufacturing Associate

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Upstream Manufacturing Associate - Biologics - cGMP Environment (Full-Time, Onsite - New Jersey, USA)

• Relocation support offered for US Citizens*

This role involves supporting cell culture operations in a fast-paced, cGMP biopharmaceutical environment focused on mammalian-based biosimilar production. Responsibilities include executing upstream processes for engineering and clinical-scale batches ranging from 50 L to 1000 L.

Key Responsibilities:

• Execute upstream manufacturing activities including cell culture and bioreactor operations at various scales
• Support the production of engineering and clinical batches in compliance with cGMP standards
• Operate and troubleshoot bioreactors, single-use systems, and associated upstream equipment
• Collaborate with cross-functional teams including engineering and quality to ensure batch readiness and execution
• Document batch execution, deviations, and investigations accurately
• Review executed batch records and supporting documentation
• Follow all safety procedures and maintain compliance with environmental, health, and safety policies
• Contribute to continuous improvement initiatives in manufacturing processes and equipment operation

Requirements:

• Bachelor's or Master's degree in Biochemistry, Chemical Engineering, Biology, or related field
• Minimum 3 years' experience in upstream biologics manufacturing in a cGMP environment
• Proficiency in aseptic technique and working with single-use technologies (bags, tubing, manifolds, etc.)
• Strong understanding of cell culture processes and bioreactor operations
• Experience initiating and executing GMP documentation including batch records and protocols
• Ability to work independently with minimal supervision and contribute to a team
• Strong attention to detail, good documentation skills, and basic computer proficiency (Word, Excel, etc.)

This position is ideal for candidates with hands-on bioprocessing experience who are confident operating in clinical and GMP-regulated settings.

Additional Details

• Seniority level: Associate
• Employment type: Full-time
• Job function: Manufacturing