Supervisor, Manufacturing Quality Assurance

Not Interested
Bookmark
Report This Job

profile Job Location:

Walker, MN - USA

profile Monthly Salary: Not Disclosed
Posted on: 12 hours ago
Vacancies: 1 Vacancy

Job Summary

This is an onsite position requiring the team member to be onsite 5 days a week.

At West were a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily Wests indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future

Theres no better place to join an inclusive community of professionals with opportunities for lifelong learning growth and development. Supported by benefit programs we empower the physical mental emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

As the Supervisor Manufacturing Quality Assurance you willmonitor and control the daily activities of quality inspection testing documentation review and calibration in support of Operations and product release.

Essential Duties and Responsibilities

  • Provides direct supervision resolves personnel issues conducts performance evaluations and performs supervisory discipline as necessary.
  • Exhibit a strong quality first mentality and ensure that product and process quality are held to the highest standard.
  • Ensures compliance with quality system documents cGMPs ISO standards and FDA regulations.
  • Schedule and prioritize quality inspection testing documentation review and calibration to support Operations and release of product.
  • Identifies and develops opportunities to improve existing processes and procedures.
  • Support quality assurance improvement activities by evaluating products processes or materials in order to develop control or improvement strategies intended to improve the customers experience.
  • Work with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence.
  • Assist in and manage the verbal communications and visual checks of work activity to ensure quality requirements are met. Ensure proper corrective actions discrepancy reports and follow up activities are accomplished. Advise on equipment condition test method etc. to aid in the course of action when components do not meet specifications. Responsible for quality inspection and verification.
  • Reviews documentation and records for accuracy. Determines if product is impacted can be released or if NonConformance Report is required.
  • Assist in developing documentation and procedures during the qualification of new equipment/inspection methods.
  • Performs other duties as assigned based on business needs.
  • Conforms with and abides by all regulations policies work procedures instruction and all safety rules.
  • Exhibits regular reliable punctual and predictable attendance.

Education

  • Education or Equivalent Experience: Associates Degree in Technical or Engineering

Work Experience

  • Experience: 5-8 years of experience in the manufacturing industry
  • 3 years of Quality supervisory experience in the manufacturing industry

Preferred Knowledge Skills and Abilities

  • Medical Device experience preferred
  • Metrology Equipment experience
  • Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
  • Support and contribute in Lean Sigma programs and activities towards delivery of the set target
  • Able to comply with the companys safety policy at all times
  • Able to comply with the companys quality policy at all times #LI-JJ1

Travel Requirements

Must be able to travel up to a minimal amount of the time.

Physical Requirements

Must be able to work assigned shift(s) with overtime as required to complete assignments if necessary. Sitting and/or standing for extended periods may occur as well as getting to and from offices and building sites. If necessitated by customer requirements must be able to see with or without corrective lenses and distinguish color differences for product and safety issues. Hearing ability should be sufficient to hear and react to audible alarms from distances up to 150 feet. The ability to be able to lift and carry various items up to 50 pounds for manufacturing positions or 30 pounds for administrative positions is required.

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race religion color national origin gender sex gender identity sexual orientation age marital status veteran status or disability status. If you have a special need that requires accommodation in orderto apply to West please send an email to . Where permitted by law an offer of employment with West Pharmaceutical Services or any of its subsidiary or affiliate companies is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.


Required Experience:

Manager

This is an onsite position requiring the team member to be onsite 5 days a week.At West were a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplyin...
View more view more

Key Skills

  • Food Safety
  • IT
  • Corporate Risk Management
  • FX
  • Airlines
  • Building Electrician

About Company

Company Logo

West Pharmaceutical Services, Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products.

View Profile View Profile