The Production Supervisor will supervise all day or swing shift production activities and ensure that processes are performed according to current standard operating procedures.
This is an in-person role, requiring on-site presence five days a week.
Specific Duties and Responsibilities
• Supervises production and pilot lines and coordinates the scheduling of people, materials, and equipment.
• Select, manage, train, and develop staff. Establish objectives and assignments and provide ongoing feedback through performance reviews and development plans.
• Interacts with production, quality control, and process engineering departments to coordinate and resolve production related issues.
• Prepares production reports and reviews log history reports.
• Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.
• Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company.
• Ensure other members of the department follow the QMS, regulations, standards, and procedures.
• Performs other work-related duties as assigned.
Position Qualifications
• High school with 2+ years of supervisory experience in manufacturing, preferably in the medical device industry, or an equivalent combination of education and experience
• Solid problem solving, decision-making, and leadership skills required
• Strong oral, written and interpersonal communication skills
• Proficiency with MS Word, Excel, Access, and Power Point
• Knowledge and understanding of FDA QSRs and ISO standards preferred
Working Conditions
• General office, laboratory, and cleanroom environments.
• Production lab/ Controlled Environment Room (CER)
• May have business travel from 0% - 10%
• Potential exposure to blood-borne pathogens
• Requires some lifting and moving of up to 25 pounds
• Must be able to move between building and floors.
• Must be able to remain stationary and use a microscope, cleanroom or laboratory equipment, or other standard office equipment, for an extensive period of time each day.
• Will need to use a computer for email, trainings, procedures, etc.
• Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.
Starting Base Salary is $50,731/year - $84,930/year.
We offer a competitive compensation package plus a benefits and equity program, when applicable.
Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.
Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures and markets novel products and has a broad portfolio that addresses challenging medical ...
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