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Temp-Manufacturing-Inspection-2nd Shfit

Alkermes · Wilmington, OH, United States

Imported listingtemporaryabout 1 month ago

About The Role

This is a temporary position.

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

KEY DUTIES

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

SKILLS/ABILITIES

  • Organization and interpersonal Skills (Oral, Written, etc.)
  • Good Computer and Database Skills
  • Comprehensive training focused on current Good Manufacturing Practices (cGMP) in the pharmaceutical industry.

PERSONAL ATTRIBUTES

  • Good math skills
  • Self-motivated
  • Good visual acuity
  • Team Oriented
  • Effective organization skills and attention to detail
  • Ability to work with minimal supervision
  • Ability to work flexible hours
  • Ability to work hands-on

PHYSICAL REQUIREMENTS

  • Prolonged periods of sitting or standing.
  • Periods of repetitive motion
  • Walking, squatting, lifting, pushing and pulling carts, reaching, climbing, and bending may all be required.
  • Steel-toe shoes, scrubs, and other PPE equipment must be worn based on the job being performed.
  • Employee must be able to pass a vision exam before employment and annually.

Qualifications

Basic Requirements

  • High School diploma or equivalent.

Preferred Requirements

  • 0-1 year experience in a sterile pharmaceutical operation preferred.
  • Associate degree or higher in a science/technical discipline

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