Process Engineer - A Shift

Job description

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. 

 

Your Role:

The Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly, and material handling. The successful candidate will be an enthusiastic team player with high energy and strong engineering skills.

 

·  Maintains efficiency and upkeep of critical manufacturing equipment through effective troubleshooting techniques.
·  Identifies and improves yield loss and scrap opportunities.
·  Develops and recommends new testing processes and technologies to achieve cost effectiveness and improved product quality.
·  Establishes operating equipment specifications and improves manufacturing techniques. Inspects performance of machinery, equipment and tools to verify their efficiency and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
·  Develops manufacturing processes that demonstrate levels of statistical control. Validates new equipment and process changes.
·  Develops and/or implements systems improvement projects and supports maintenance and production groups in resolving technical and engineering issues.
·  Provides process on assigned Corrective Action Preventive Action (CAPA). Trains departmental technicians and operators to ensure sufficient expertise exists within the manufacturing work centers.
·  Reviews capital equipment fabrication activities to ensure manufacturing, construction, installation, and operational testing conform to functional specifications, regulatory safety standards, and user requirements.
·  Investigates and develops new processes required to improve manufacturing operations and processes.
·  Develops cost estimates, obtains quotes, and generates capital requests to support new processes and capital equipment purchase.
·  Leads and participates in Equipment and Process Validations activities per Current Good Manufacturing Practices (cGMP) regulations for Medical Device manufacturing.
·  Ensures that product quality features meet product specifications and comply with process validation requirements.
·  Generates, reviews and approves engineering, manufacturing and quality procedures necessary to support equipment validation/revalidation, launch, and normal production schedules.
·  Facilitates training for individuals involved with the operation and maintenance of processes and equipment introduced to the manufacturing department.
·  Generates engineering procedures and reviews and approves manufacturing standard operating procedures.
·  Develops validation protocols and reports in support of cGMP requirements. Initiate, reviews/approves change requests, and develops implementation solutions to support operational needs.
·  A Shift: Monday - Friday 8:00AM - 4:30PM

 

Who you are:

Minimum Qualifications:

·  Bachelor of Science Degree in Electrical, Mechanical or Chemical Engineering
·  1+ years' of experience in an FDA regulated medical device manufacturing facility or pharmaceutical facility 

OR

·  Associate Degree in a technical field and 2+ year' work experience in an FDA regulated medical device manufacturing facility or pharmaceutical facility

 

Preferred Qualifications:

·  Instrumentation and PLC / code knowledge
·  Lean 6 Sigma experience
·  Green or Black belt 

 

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.

Job Requisition ID:  256626

Location:  Jaffrey

Career Level:  C - Professional (1-3 years)

Working time model:  full-time .buttontext1722e80f7dc3f6d2 a{ border: 1px solid transparent; } .buttontext1722e80f7dc3f6d2 a:focus{ border: 1px dashed #eb3c96 !important; outline: none !important; }

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, 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.

Notice on Fraudulent Job Offers
Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information .

Nearest Major Market: Bellows Falls
Nearest Secondary Market: Keene
Job Segment: Pharmaceutical, Six Sigma Black Belt, Medical Device, Lean Six Sigma, Developer, Science, Management, Healthcare, Technology