Quality Engineering Supervisor - A Shift

Posté 02 nov. 2022

Jaffrey, New Hampshire - United States

Demander un identifiant 257962

 

A career with MilliporeSigma is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

 

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.


Your Role:

 

We are seeking a motivated Quality Engineering Supervisor to support device manufacturing at the Jaffrey Manufacturing site. This position will manage a small team of Quality Engineers and Quality Technicians and oversee three rapidly growing manufacturing work centers, partnering with Operations, Engineering, Product Management (Marketing) and EHS. The candidate’s ability to apply fundamental engineering techniques and lean/six sigma principles to improve product performance is crucial to this role. The Supervisor will provide guidance and mentorship to their growing team of quality engineers and quality technicians.

In addition to the supervisory requirements, the candidate will also be responsible for providing day-to-day Quality Engineering support for a fast-paced device manufacturing operation, including:

  • Evaluation of out-of-specification conditions and providing mentorship for the disposition of non-conforming product and raw materials
  • Leading quality investigations (RCA and CAPA management)
  • Perform statistical analysis and trending to assess and monitor product/process performance
  • Working with multi-functional teams to set the requirements to support product and process modifications; ensuring that Change Control requirements are met based on internal company procedures and applicable industry standards and regulations
  • Lead and participate in the creation of risk assessments (product and process- FMEA)
  • Participate in product validation and equipment qualifications by establishing acceptance criteria, statistical sampling plans, data analysis, and write validation protocols and reports
  • Build / revise Standard Operating Procedures, Test Methods, and other documents 
  • A Shift: Monday - Friday 8AM - 4PM

 

Who You Are:

Minimum Qualifications:

  • Bachelor's of Science Degree in a Scientific, Engineering, or Technical discipline
  • 2+ years' of Quality Engineering experience 

 

Preferred Qualifications:

  • Leadership experience in an FDA regulated environment (pharmaceutical, biotechnology, or medical device)
  • Understanding or experience with ISO & FDA regulations (such as 21 CFR 820, 210 & 211)
  • Demonstrated ability to conduct quality investigations including root cause analysis and determining corrective / preventative actions
  • Strong communication skills with the ability to collaborate with Customers and at all levels and functions of the organization
  • Pragmatic risk-based decision maker with strong problem-solving ability 
  • Collaborative and motivated team player. Always looking to share and advance best practices
  • Experience with relevant data analysis software (i.e., Minitab)
  • Working knowledge of Electronic Quality Systems (CAPA, Change Control, Documentation Management)
  • Black Belt or Green Belt 
  • ASQ or CQE 

 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences.
We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

If you are a resident of Colorado or New York City, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

As an employee of the Company, you will be required to comply with all of the Company’s COVID-19 safety protocols and policies. The organization has currently suspended enforcement of its COVID-19 Vaccination Policy, but that policy may be reinstated by the Company in its discretion.

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