| Job Description | Description
The Sr. Supervisor/Manufacturing Manager reports to the Manufacturing Director and has oversight responsibility for any of the manufacturing operations in either the SVP or Allergenics manufacturing departments. The Primary responsibility of the Sr. Supervisor/Manufacturing Manager will be to manage the personnel and processes involved in the production of liquid parenterals in the SVP and/or Allergenics manufacturing operations. Technical knowledge of aseptic processing, cGMP’s, FDA regulations, and organizational, and managerial, leadership skills will be used to effectively manage the department. This position has functional responsibility for Packaging and SVP Lines 1 & 2. Essential responsibilities are to:
Manage all manufacturing activities occurring on all shifts. This includes, but is not limited to the following areas: Mycology, Raw Materials/Extractions, Supply Preparation, Sterile Filtration, Sterile Filling, Finishing, SVP production, SVP packaging, and all cleanroom sanitization activities.
Ensure a safe workplace and that all job activities are performed in a safe manner.
Administer disciplinary action, and provide coaching and counseling to improve the performance and morale of the Manufacturing department.
Maintain knowledge of state of the art parenteral manufacturing concepts, practices, and processes, including cGMP’s, and Aseptic Processing Guidelines.
Ensure that documented training, attendance, and performance records are maintained.
Conduct performance reviews and set objectives for manufacturing supervisors. Review and approve performance reviews and objectives for non-exempt employees.
Interview and hire employees. Ensure documented training of all employees.
Ensure that all production schedules are met. Communicate and coordinate priorities with Production Planning. Communicate with the Maintenance department regarding repair or preventative maintenance of machinery as required.
Review and challenge existing methods of production with the goal of increasing efficiencies and improving quality.
Order or approve purchase requests for production supplies and non-capital operating equipment. Recommend and provide guidance relating to the purchase of capital equipment.
Complete annual expense and capital budgets.
Ensure that all production activities are accurately described in written procedures, and that these procedures meet with cGMP requirements.
Qualifications:
Bachelor of Science in Biology, Chemistry or other hard science. 2 years of closely related experience can be used in lieu of degree in hard sciences for Senior Supervisor level, as long as the applicant has a Bachelor's degree. 3 years of closely related experience can be used in lieu of degree in hard sciences, as long as the applicant has a Bachelor’s degree.
A minimum of 5 years pharmaceutical and supervisory experience is required. Managerial experience is desired.
Proficiency is required in Microsoft Word, Excel and PowerPoint.
Physical Requirements: 20/20 corrected vision, working in aseptic areas, and exposure to allergens. Some travel.
SALARY $59,350 Min to $92,775 Mid DOQ |
| | Company | | Jubilant HollisterStier Contract Manufacturing & Services | Job Code | | State or Province | | Washington | | |
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