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Production Supervisor

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.


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CEO of Penumbra
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Adam Elsesser
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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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Full-time, on-site
DATE POSTED
October 20, 2024

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