Manufacturing Associate II/III/Sr.-2nd Shift

Alkermes • Wilmington, OH

173d

About The Position

The position involves inspecting GMP (Good Manufacturing Practices) vials, including both product and glass vials, for defects. The role also includes performing label and packaging activities for the finished product. The candidate will be responsible for ensuring compliance with standard operating procedures (SOPs) and current good manufacturing practices (cGMP).

Requirements

• High School Diploma or equivalent
• 1-3 years of pharmaceutical manufacturing or equivalent experience

Nice To Haves

• 1+ year experience in a sterile pharmaceutical operation
• Associates degree or higher in a science/technical discipline
• Vial or general inspection experience preferred
• 4-5 years experience in pharmaceutical Manufacturing
• 2-3 years experience in a sterile pharmaceutical operation
• Training experience

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 the area’s process documents
• Operate equipment in compliance with SOPs
• Assure compliance with cGMP requirements
• Work non-routine hours as required to maintain production schedule
• Perform label and packaging activities for the 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

What This Job Offers

• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 1,001-5,000 employees