Penumbra, Inc.
Production Manager
Penumbra, Inc., Alameda, California, United States, 94501
Manage all production activities and ensure that processes are performed according to current standard operating procedures.Drive continuous improvement in the areas of yield, throughput, cycle time, and efficiency.The Production Manager plays a key role in both production planning, and the control and supervision of production.This position has the following work schedule: Monday through Friday, 3 pm to 11:30 pm.Specific Duties and Responsibilities
Oversee the production process and schedule.Ensure that production is cost effective by estimating production costs.Ensure timeliness of finished products by monitoring production processes and maintaining schedules.Determine human and material resource requirements.Establish and maintain quality standards; implement quality control programs.Liaise among different departments, e.g., purchasing, engineering, etc., working with managers to implement the company's policies and goals.Ensure that health and safety guidelines are followed.Participate in the selection, training, mentoring, and evaluation of Production Supervisors and Training Coordinators.Identify training needs.Select, manage, train, and develop staff. Establish objectives and assignments and provide ongoing feedback through performance reviews and development plans.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.Perform other work-related duties as assigned.Position Qualifications
Bachelor’s degree with 5+ years of supervisory experience in the medical device or related industry, or an equivalent combination of education and experience.Strong verbal, written and interpersonal skills are required.Demonstrated ability to motivate and develop team members and to address performance issues effectively.Experience with MRP and lean manufacturing highly desired.Ability to work Monday through Friday, 7 am to 3:30 pm.Working Conditions
General office, laboratory, and cleanroom environments.Willingness and ability to work on site. 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 buildings 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
$110,000/year - $175,000/year plus differential. Individual compensation will vary over time based on factors such as performance, skill level, competencies, work location, and shift.
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Oversee the production process and schedule.Ensure that production is cost effective by estimating production costs.Ensure timeliness of finished products by monitoring production processes and maintaining schedules.Determine human and material resource requirements.Establish and maintain quality standards; implement quality control programs.Liaise among different departments, e.g., purchasing, engineering, etc., working with managers to implement the company's policies and goals.Ensure that health and safety guidelines are followed.Participate in the selection, training, mentoring, and evaluation of Production Supervisors and Training Coordinators.Identify training needs.Select, manage, train, and develop staff. Establish objectives and assignments and provide ongoing feedback through performance reviews and development plans.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.Perform other work-related duties as assigned.Position Qualifications
Bachelor’s degree with 5+ years of supervisory experience in the medical device or related industry, or an equivalent combination of education and experience.Strong verbal, written and interpersonal skills are required.Demonstrated ability to motivate and develop team members and to address performance issues effectively.Experience with MRP and lean manufacturing highly desired.Ability to work Monday through Friday, 7 am to 3:30 pm.Working Conditions
General office, laboratory, and cleanroom environments.Willingness and ability to work on site. 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 buildings 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
$110,000/year - $175,000/year plus differential. Individual compensation will vary over time based on factors such as performance, skill level, competencies, work location, and shift.
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