Manufacturing Associate Role at Catalent
Catalent Pharma Solutions is seeking a Manufacturing Associate to support their GMP pharmaceutical production operations in Chelsea, Massachusetts. This full-time night shift role at Catalent Careers involves hands-on execution of spray drying, equipment operation, sanitation, and process troubleshooting within a state-of-the-art Center of Excellence for Dry Powder Inhaler (DPI) manufacturing. Apply for the Life Science Jobs in USA.
Job Details:
- Position: Manufacturing Associate (Night Shift)
- Location: Chelsea, Massachusetts, 02150, USA
- Job ID: 0091001
- Work Type: Full-time, On-site
- Overtime & Holiday Pay: Included
- Salary Range: $60,445 โ $89,280 annually (based on experience, education, and location)
Shift Details for the Manufacturing Associate Role:
- 7-day rotating (Pitman Schedule), 12-hour shifts (6:00 p.m.โ6:00 a.m.)
- Week 1: 48 hours (4 days)
- Week 2: 36 hours (3 days)
About the Company:
Catalent, Inc. is a global CDMO dedicated to developing, manufacturing, and supplying high-quality pharmaceutical, biotech, and consumer health products. With over 40 global sites and thousands of skilled scientists and technicians, Catalent is a leader in spray drying, DPI manufacturing, and multi-modality production. The company focuses on innovation, patient-first values, compliance, and supporting the life cycle of hundreds of products each year.
Educational Requirements for the Manufacturing Associate Role:
Candidates must meet one of the following criteria:
- High school diploma/equivalent + 5 years of experience
- Biotechnology Certificate or Associateโs Degree + 3 years of experience
Additional expectations:
- Experience operating automated manufacturing control systems (preferred)
- Familiarity with parts washers, autoclaves, documentation, and GMP compliance
- Proficiency with Microsoft Office Suite
- Ability to lift up to 50 lbs and perform physical tasks
Key Responsibilities of the Manufacturing Associate Role:
- Perform Clean-In-Place (CIP), Clean-Out-of-Place (COP), and equipment sanitization
- Operate and monitor manufacturing equipment for GMP pharmaceutical production
- Execute routine and complex spray drying processes
- Troubleshoot manufacturing equipment to resolve process issues
- Receive, verify, and distribute supplies within manufacturing
- Provide feedback on procedural and process improvements
- Support SOP revisions and continuous improvement initiatives
- Complete equipment inspection, documentation, and compliance tasks
- Perform other duties as assigned
Skills Required for the Manufacturing Associate Role:
- Strong understanding of cGMP and Good Documentation Practices
- Ability to follow and execute complex SOPs
- Experience with automated systems, parts washers, and autoclaves
- Process troubleshooting skills
- Ability to work night shifts in a fast-paced environment
- Strong technical, communication, and problem-solving skills
- Physical capability to lift 50 lbs and perform routine motion-based tasks
How to Apply?
Candidates interested for the Life Science Jobs can apply through the official Catalent Careers website. Applicants may also sign up for job alerts, create a profile, and track applications through the portal.
