Job Description
Job Title: Purification Manufacturing Consultant
Location: Pennington, NJ (100% Onsite)
Shifts: Must be flexible for either 8am–4:30pm or 3pm–11pm EST
Overview:
Seeking a hands-on Purification Manufacturing Consultant to support both facility start-up activities and cGMP biopharmaceutical manufacturing operations. This role plays a key part in launching and sustaining a high-performing production site.
Key Responsibilities:
- Support facility commissioning, equipment selection, protocol development, and technical training
- Execute cGMP operations including buffer prep, CIP/SIP, filtration, and chromatography
- Follow automated batch records and ensure strict compliance with SOPs and quality standards
- Troubleshoot processes and equipment, identify deviations, and contribute to continuous improvement
- Develop and optimize cGMP procedures and documentation
Requirements:
- High school diploma or GED required; AS/BS in a science-related field preferred
- Strong communication skills and ability to work in fast-paced, team-driven environments
- Physically capable of lifting up to 40 lbs, standing for long periods, and working with hazardous materials
- Willing to work onsite and flexible with shift assignments and potential overtime
Ideal Candidate:
- Detail-oriented with a passion for continuous improvement
- Comfortable with complex systems and eager to grow in a dynamic manufacturing setting
- Prior experience in purification or biopharmaceutical environments is a strong plus
Job Tags
Flexible hours, Shift work,