We are seeking a Bioprocessing Associate II to join our Manufacturing Downstream team. This role supports the production of biological products in a cGMP-compliant environment. If you have experience in production within Biologics, Biotech, or Life Sciences, and transferrable skills in Blending, Aseptic, and Compounding, will thrive in this position.
Schedule: Wednesday - Saturday, 6:00am-4:30pm OR Sunday- Wednesday, 6:00am-4:30pm
Pay: $25-$30/hr can go higher with experience
Location: Cranbury, NJ
Key Responsibilities:
Maintain a safety-oriented, cGMP-compliant work environment.
Assist with facility and equipment start-up activities as needed.
Support production teams to achieve output targets and maintain quality standards.
Prepare shift duties, including checking buffer and material/consumable requirements.
Perform production operations according to SOPs and Manufacturing Batch Records.
Contribute to Continuous Improvement initiatives using Lean/Six Sigma tools.
Report deviations from SOPs or standard production processes immediately.
Maintain facility housekeeping standards.
Complete all required training and ensure ongoing compliance.
Adhere to all safety policies, procedures, and regulations.
Perform duties in accordance with GMP requirements and controlled documents.
Take on additional tasks as assigned by the Manufacturing Supervisor.
Qualifications:
Certificate, Diploma, Degree, or equivalent experience in Science, Engineering, or a related field.
0–2 years of experience in biopharmaceutical cGMP manufacturing.
Experience in clinical phase or biopharmaceutical manufacturing is a plus.
Knowledge of GMP and biotech manufacturing processes.
Basic understanding of bioprocessing/biotechnology and relevant equipment (bioreactors, centrifuges, autoclaves, media/buffer systems, purification systems).
Ability to work with complex electronic systems, such as process automation, SAP, and Trackwise.
Behavioral Competencies:
Strong communication, interpersonal, and presentation skills.
Collaborative, inclusive, and flexible team player.
Problem-solving and troubleshooting abilities.
Self-starter with initiative and autonomy.
High ethical standards and commitment to regulatory compliance and quality.
