Manufacturing Associate I-Inspection-2nd Shift

To inspect GMP (Good Manufacturing Practices) vials (product and glass vials) for defects and perform label and packaging activities for finished product.

Responsibilities:
- Inspect vialed product and empty glass for defects
- Perform daily process activities per standard operating procedures (SOPs)
- Prepare process-specific and ancillary equipment (e.g., glassware, apparatus)
- Assist in writing and implementing area process documents
- Operate equipment per SOPs
- Assure compliance with cGMP (current good manufacturing practices)
- Work non-routine hours as required to maintain the production schedule
- Perform label and packaging activities for finished product
- Complete and review production records and daily trending
- Train new inspectors per vial inspector certification procedures
- Assist other manufacturing functions (Formulation, Fill, Materials) as required

Skills/Abilities:
- Organization and interpersonal skills (oral, written)
- Good computer and database skills
- Comprehensive cGMP-focused training in the pharmaceutical industry

Qualifications:
- High school diploma or equivalent
- Preferred: 0–1 year experience in a sterile pharmaceutical operation
- Preferred: Associate degree or higher in a science/technical discipline

Personal attributes (relevant to role):
- Good math skills; self-motivated; good visual acuity; team-oriented
- Attention to detail; ability to work with minimal supervision
- Ability to work flexible hours; hands-on

Physical requirements:
- Prolonged sitting/standing; repetitive motion; walking/squatting/lifting/pushing/pulling/reaching/climbing/bending
- Wear steel-toe shoes, scrubs, and required PPE; pass vision exam before employment and annually