Jobs with Alkermes, Inc.
(Found 128 Jobs)
Temp-Visual Inspector
Alkermes, Inc.
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....
Sep 18, 2024
Wilmington, OH
Senior Systems Analyst (R&D)
Alkermes, Inc.
Position: Senior Systems Analyst
Company Overview:
Alkermes plc is a fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS...
Sep 17, 2024
Waltham, MA
Director, Clinical Quality Assurance, Pharmacovigilance
Alkermes, Inc.
The Director of CQA-PV is the supervisor of the Clinical Quality Assurance Department with responsibilities for quality oversight of the Post Marketing Good Pharmacovigilance Practices (GPvP) and Comm...
Sep 4, 2024
Waltham, MA
Territory Business Manager Psychiatry – Western MA
Alkermes, Inc.
Territory Business Manager (TBM) is responsible for selling Alkermes products in the Western MA territory and supporting promotional efforts. Ideal candidates should be proven sales achievers and live...
Aug 25, 2024
Springfield, MA
Temp-Manufacturing Associate-Bulk-2nd Shift
Alkermes, Inc.
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, a...
Aug 25, 2024
Wilmington, OH
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
