Production Supervisor - Swing shift
ExternalMANAGERSupply ChainNeurologyMasters
$70K - $110K/yr(estimated)
Description
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 *.
• Work Order Management: Ensure work orders are processed in a timely manner, proactively identifying and addressing any delays*.
• Collaborate with Planning on delayed work orders to determine mitigation actions and prevent backorders*.
• Maintain an environment of continuous improvement, lean manufacturing and efficiency through lean principles, employee coaching, kaizen events and KPI monitoring*.
• Meeting Engagement – Attend and participate in the master schedule meetings and drive team to meet the daily, weekly, and monthly goals without compromising quality.
• Address and escalate line issues as needed*.
• Process Ownership – Supervisors must maintain a strong presence on their lines, understand, own, and clearly communicate their processes to stakeholders while collaborating with engineering on technical issues*.
• 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 *
• Adherence to all local, state and federal laws which include but not limited to wage and hour
• 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, Required
• 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
Position Qualifications, Preferred
• 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.
Annual Base Salary Range: $70,304 - $110,000 plus differential
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
MEDICAL DEVICES
Vascular / Surgical Devices
LocationALAMEDA, CA
Open Jobs71
Cardiovascular
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