Temp Vial QC Inspector – 2nd Shift

Alkermes; Wilmington (DE); On-site; USD 25,000 - 30,000; Full time

Job summary

Alkermes in Wilmington, Delaware is hiring a temporary vial inspector to support inspection of GMP vials and label/packaging of finished product. You will examine vialed product and empty glass for defects and perform daily process activities per SOPs.

Ideal candidates have a High School diploma (Associate degree preferred) and 0–1 year in a sterile pharmaceutical operation; strong organizational, computer and data skills, and ability to work flexible hours. Training on cGMP provided.

Qualifications

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

Responsibilities

• 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

Organization skills

Computer skills

cGMP training

Education

High School diploma

Associate degree or higher in science/technical

Job description

Alkermes in Wilmington, Delaware is hiring a temporary vial inspector to support inspection of GMP vials and label/packaging of finished product. You will examine vialed product and empty glass for defects and perform daily process activities per SOPs.

Ideal candidates have a High School diploma (Associate degree preferred) and 0–1 year in a sterile pharmaceutical operation; strong organizational, computer and data skills, and ability to work flexible hours. Training on cGMP provided.