Manufacturing AssociateCatalent • Chelsea, MA, US
Manufacturing Associate
Catalent • Chelsea, MA, US
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job_description.job_card.job_descriptionA high school diploma or equivalent combined with five (5) years of experience, OR a Biotechnology Certificate or Associate's Degree in science related field combined with three (3) years of experience is required. Experience with operating automated manufacturing control systems is preferred Experience utilizing parts washers and autoclaves for the preparation of manufacturing and / or laboratory equipment Critical understanding of the importance of documentation and data traceability Extensive familiarity with executing Standard Operating Procedures in a manufacturing or assembling environment, preferably in the pharmaceutical industry Must have experience with Microsoft Office Suite. Strong working knowledge of Good Documentation and current Good Manufacturing Practices Defined career path and annual performance review and feedback process Diverse, inclusive culture Positive working environment focusing on continually improving processes to remain innovative Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 152 Hours + 8 paid holidays Generous 401K match Medical, dental and vision benefits effective day one of employment
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply.
The Boston-area facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging.
Job Summary
Catalent Pharma Solutions in Boston is hiring a Manufacturing Associate. The Manufacturing Associate performs routine and complex operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines.
This is a full-time, on-site, hourly role. Work schedule will be a 7-day rotating 12-hour schedule from 6 : 00 p.m. to 6 : 00 a.m. Overtime and Holiday pay will be included.
Responsibilities
- Performs Clean-In-Place, Clean-Out-of-Place, and equipment sanitization
- Operates and monitors manufacturing equipment for the production of clinical and commercial pharmaceutical products under minimal supervision
- Executes routine and complex production processes
- Troubleshoots manufacturing equipment in conjunction with supporting functional groups to resolve issues and optimize process
- Provides feedback to manager on recommendations for procedural and process improvements
- Utilizes process knowledge to influence positive change during the review and revision of Standard Operating Procedures (SOPs)
- Participates in continuous improvement activities and projects as needed
Requirements
What We Offer
Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to DisabilityAccommodations@catalent.com.
J-18808-Ljbffr
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