Upstream Processing Manufacturing Associate

Pharma Universe; Piscataway Township (NJ); On-site; USD 60,000 - 100,000; Full time

Job summary

An innovative company in the biopharmaceutical sector is seeking talented Upstream Processing Manufacturing Associates to join their dynamic team. This role is essential as they transition from pilot manufacturing to full-scale commercial production in their new facility. Candidates will work with cutting-edge technology in mammalian cell culture and bioreactor operations, ensuring compliance with stringent GMP standards. If you have a passion for biomanufacturing and a desire to contribute to the production of life-saving biologics, this opportunity is perfect for you.

Qualifications

• 1-2 years of experience in cell culture and bioreactor operations.
• Proficiency in GMP and aseptic manufacturing practices.

Responsibilities

• Execute mammalian cell culture processes for recombinant protein production.
• Operate bioreactors and improve manufacturing techniques.
• Review and document manufacturing records for GMP compliance.

Skills

Mammalian Cell Culture

Bioreactor Operations

Aseptic Manufacturing

GMP Compliance

Single-Use Manufacturing Consumables

Education

Bachelor's Degree in Life Sciences

Relevant Certifications

Job description

Upstream Processing Manufacturing Associate

We are hiring seven Upstream Manufacturing Scientists/Associates at various experience levels to support our growth as we scale from pilot manufacturing to full-scale commercial production at our new NJ facility.

Positions Available:

• Manufacturing Scientist I - III - from 1 year of experience+

Responsibilities:

• Execute mammalian cell culture processes to produce recombinant proteins for biologics, managing cell culture batches up to 2000L.
• Operate bioreactors, establish equipment specifications, and improve manufacturing techniques.
• Collaborate with manufacturing associates and engineers, providing guidance.
• Initiate batch records, protocols, and oversee investigations in a cGMP environment.
• Review and document manufacturing and packaging batch records, ensuring safety and GMP compliance.

Qualifications:

• At least 1-2 years of experience in cell culture and bioreactor operations, including GMP and aseptic manufacturing.
• Proficiency with single-use manufacturing consumables and experience in scale-up manufacturing.

Additional Details:

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