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Supervisor, Manufacturing - Night Shift - Chelsea Massachusetts
Company: Disability Solutions Location: Chelsea, Massachusetts
Posted On: 04/18/2024
We're hiring for a night shift Maintenance Supervisor to provide operational leadership for our manufacturing operations team in the Boston area!Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.--The Maintenance Supervisor is responsible for leading a team of four operators in the execution of routine and complex operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines.-- This individual is responsible for the hands-on execution of production activities and task assignments to direct reports as they relate to spray drying operations of manufactured products. This is a full-time, salaried position and is 100% site based. The schedule is a rotating night shift with hours of 6:00PM - 6:00AM, with every other weekend off. --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. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America.Catalent is committed to a Patient First culture through excellence in quality and--compliance, and to the safety of every patient, consumer, and Catalent employee.--The Role - Performs Clean-In-Place, Clean-Out-of-Place, and equipment sanitization.
- Operates and monitors manufacturing equipment to produce clinical and commercial pharmaceutical products and directs team members in to perform tasks necessary to meet the manufacturing schedule.
- Executes routine and complex production processes.
- Troubleshoots manufacturing equipment in conjunction with supporting functional groups to resolve issues and optimize process.
- Performs inspection of equipment and documents.
- Receives and distributes supplies in the manufacturing area.
- 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).
- Trains team members on the execution of Standard Operating Procedure.
- All other duties as assigned.The Candidate
- High school diploma or equivalent, combined with 5-8 years of experience.
- Biotechnology certificate or associate degree in science-related field, combined with 3-5 years of experience.
- Bachelor's degree in life sciences or engineering field, combined with 1-3 years of experience.
- Prior leadership experience highly preferred.
- Extensive familiarity with executing Standard Operating Procedures (SOPs), Good Documentation (GDP) and current Good Manufacturing Practices (cGMP), in a manufacturing or assembling environment, preferably in the pharmaceutical industry.
- Demonstrated ability to perform product and/or process investigations preferred. Why you should join Catalent
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