Job description


Quality Supervisor (0872)

Group Company:
  • Mitsubishi Chemical Performance Polymers

Mitsubishi Chemical Performance Polymers, Inc. (MCPP) a subsidiary of Mitsubishi Chemical is wholly owned, MCC and its twenty group companies provide products and services to customers in North and South America providing a broad range of businesses including chemical, petrochemical, composite materials, pharmaceuticals, electronics, and other businesses.

MCPP has doubled in size over the past 5 years due to the organic growth with our customers as well as numerous positive acquisitions. This has allowed us to expand our product portfolio, global reach and create an exceptional team of 1000+ dedicated employees. MCPP operates a global network of 24 sites in 15 nations. In the Americas, MCPP has locations in Michigan, Ohio, South Carolina and Brazil.

MCPP's goal to our associates is to create an environment that motivates people, creates teamwork and encourages close collaboration with our customer and suppliers. We maintain a strong investment in our associates and encourage an entrepreneurial spirit and growth. We offer our associates a competitive salary, benefits, vacation and incentive package. We encourage learning and development and offer our associates opportunity for advancement. 

Job Purpose

Mitsubishi Chemical Performance Polymers (MCPP) Quality Supervisor will manage daily activities including quality release of commercial product, batch record sign off, nonconformance investigations, audits, CAPA, validations, training, safety, release of raw materials, management representative

Principal Accountabilities


The functions below are not all inclusive of the duties for this position.  Other responsibilities may be assigned as deemed necessary.

  1. Develop and maintain quality systems including internal and external audits, change control, material control, facilities and equipment, investigations, management of the CAPA program and QC policies.
  2. Write, review, approve and implement product quality related policies and SOP’s as required.
  3. Responsibilities also include performing documentation review of batch manufacturing and QC test records for compliance and release of final product, auditing, reviewing and approving    process documents and technical reports.
  4. Designing and implementing training programs for employees.
  5. ISO Representative
Knowledge / Skills / Experience


  1. Four year degree in engineering or a technical related discipline or equivalent in work experience (ten years).
  2. In lieu of the above, a four year degree in life sciences a plus but not necessary.


  1. 10+ years experience in the medical device, pharmaceutical or biotechnology industry is preferred.
  2. Experience with third party audits and FDA inspections as well as a strong understanding of qualification and validation requirements
  3. Strong knowledge of FDA guidelines and regulations regarding cGMP’s - Outstanding written and verbal skills as well as problem solving skills.
  4. Demonstrated team player with experience contributing to multi-disciplinary project teams and ability to work with minimal supervision.
  5. Strong initiative and ability to assume significant project management skills. - Ability to work in a fast-paced and dynamic environment. 


EEO Statement

Mitsubishi Chemical Corporation values diversity in the workplace, is committed to a policy of equal employment opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or any other legally recognized protected basis under applicable law.
Applicants with disabilities may be entitled to a reasonable accommodation under the Americans with Disabilities Act and/or other applicable laws. If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition.

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