Production Supervisor - Swing shift

Penumbra • Roseville, CA

1d • Onsite

About The Position

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.

Requirements

• 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

Nice To Haves

• Knowledge and understanding of FDA QSRs and ISO standards preferred

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.

Benefits

• A collaborative teamwork environment where learning is constant, and performance is rewarded.
• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
• A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Education Level: High school or GED