Job Details

Job Responsibilities

• Review production/mfg. plans, docs, etc.
• Support other depts. & other shifts as needed
• Provide management with status updates of projects to ensure efficiency
• Support R&D projects
• Ensure all working areas are clean & organized for efficiency
• Manage & review final product & packages
• Review & update BOMs
• Review & update QMR
• Perform other duties as necessary

Job Requirements

• 5+ years of relevant bench experience – Experience with biopharma downstream processing
• Familiarity with cGMP & ISO requirements
• Experience with protein purification techniques, cell-culture/mAB/hybridoma production/purification
• Ability to lift up to 50 lbs.
• Willing to work in/travel to various company locations here locally
• Willing to travel to trade shows & client sites
• Excellent written & verbal communication skills
• Strong problem-solving & critical thinking skills