Production Supervisor
Penumbra
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.
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.
Confirm your E-mail: Send Email
All Jobs from Penumbra