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

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