About this opportunity
Planet Pharma lists this Upstream Manufacturing Associate I opportunity in pennington, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
CONTRACT : 6 month contract to start with the potential to extend and convert to full-time
For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.
Shifts available :
2nd shift: 2pm-10pm
3rd shift: 10pm-6am
MUST HAVES:
Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or a related discipline with 0-2 years of relevant experience
Position Overview
The Upstream Manufacturing Associate I provides support for upstream manufacturing activities within a cGMP environment.
Key Responsibilities
Upstream Processing
Perform cell culture activities including vial thaw, seed train expansion, fed-batch and perfusion bioreactor operations.
Oversee harvest and filtration operations.
Monitor critical process parameters and implement corrective actions when required.
Troubleshoot process and equipment issues to ensure uninterrupted operations.
In-Process Testing
Perform and review manufacturing support testing utilizing:
Cedex Cell Analyzer
Blood Gas Analyzer (BGA)
Osmometer
Other process monitoring equipment
Documentation & Compliance
Assist with preparation and revision of: Standard Operating Procedures (SOPs), Master Batch Records (MBRs), and Manufacturing forms/templates
Support deviation investigations, CAPAs, and change controls.
Ensure ongoing inspection readiness and GMP compliance.
Participate directly in regulatory and client audits.
Cross-Functional Coordination
Coordinate activities between Manufacturing, QA, QC, MSAT, Warehouse, Facilities, and Supply Chain teams.
Support process validation, technology transfer, and commercial manufacturing initiatives.
Drive continuous improvement and operational excellence projects.
Qualifications
Education & Experience
Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or a related discipline with 0-2 years of relevant experience.
High School Diploma/GED with 4+ years of relevant biopharmaceutical manufacturing experience may be considered.
Required Skills
Basic understanding of biological manufacturing and cell culture processes.
Ability to follow detailed instructions and procedures.
Strong attention to detail and documentation practices.
Effective communication and teamwork skills.
Knowledge of cGMP requirements is preferred.
Preferred Skills
Experience with:
Cell culture operations
Shake flask cultivation
Bioreactor systems
Buffer and media preparation
Single-use technologies
Aseptic processing
Physical Requirements
Ability to stand for extended periods. xzgxqkn
Ability to bend, reach, and lift up to 50 pounds.
Ability to work in cleanroom environments while wearing required PPE.
Worksite address
pennington, NJ, 08534, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.