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Biomanufacturing Supervisor

4 weeks ago


Madison, Wisconsin, United States Catalent Pharma Solutions Full time

The **Biomanufacturing Supervisor** oversees the processes, procedures, and personnel performing a variety of duties, including work order management, inventory management, material handling, and providing support to Materials Management and Biomanufacturing teams.

Catalent is a global, high-growth company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your skills, expertise, and passion are essential to our mission: to help people live better, healthier lives.

**Shift:** Monday-Friday 2pm-10pm

**Key Responsibilities:**

* Ensure work order staging schedules are adhered to and work orders are staged in-full, correctly, and in a timely manner.

* Support Biomanufacturing staff by fulfilling material requests and staging materials appropriately.

* Support Materials Management staff with participation in Cycle Count activities, as well as removing expired materials from manufacturing spaces and material storage spaces.

* Display ownership of work order management, including pulling materials and maintaining a report of work order staging status.

* Hire, train, motivate, lead, develop, and evaluate staff. Take corrective action as necessary on a timely basis and in accordance with company policy.

* Provide team with training of daily activities and approve training forms.

* Develop, implement, and enforce training materials specific to your team and/or department.

**Requirements:**

* Bachelor's Degree or Associate's Degree in a related field with a minimum of 2 years of relevant experience, including demonstrated career progression and leadership responsibilities, OR

* High school diploma with a minimum of 5 years of relevant experience.

* Individuals with prior cold storage material handling experience, operating hand scanner experience, prior pharmaceutical or food manufacturing/processing experience, and prior cGMP and Good Documentation Practices (GDP) experience are preferred.

**Why Catalent:**

* Competitive medical benefits and 401K

* 152 hours PTO + 8 Paid Holidays

* Dynamic, fast-paced work environment

* Opportunity to work on Continuous Improvement Processes

**Catalent offers rewarding opportunities to further your career**. Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma, and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.