Manufacturing Engineer II

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POST DATE 8/16/2016
END DATE 10/12/2016

MilliporeSigma Danvers, MA

Company
MilliporeSigma
Job Classification
Full Time
Company Ref #
150784
AJE Ref #
575891039
Location
Danvers, MA
Experience
Mid-Career (2 - 15 years)
Job Type
Regular
Education
Bachelors Degree

JOB DESCRIPTION

APPLY
MilliporeSigma plays an integral part in the life science community, harnessing our passion and innovation to help researchers and drug producers around the world. As science advances, we advance with it, offering new insight and cutting-edge technologies helping our customers solve the world's most challenging human health issues. Our promise to our customers is that we'll be there every step of the way. MilliporeSigma is a division of Merck KGaA, Darmstadt, Germany. Merck KGaA, Darmstadt, Germany is a global pharmaceutical and chemical company with a history that began in 1668, and a future shaped by around 40,000 employees in 64 countries.

The Mobius Operations organization in Danvers, MA is seeking an experienced Manufacturing Engineer to join our Mobius Manufacturing Engineering team in Danvers, MA.

This position will be primarily responsible to develop and maintain innovative mechanical and automated solutions to continuously improve the Mobius operation.



Duties and Responsibilities

Develop, evaluate, improve and document manufacturing processes.

Develop and implement process control techniques and procedures into manufacturing environments.

Analyze manufacturing process flows continually for the enhancements of quality, cost reduction, and throughput. Support and also lead Process Excellence initiatives.

Collaborate with designers and engineering regarding product tooling and design to ensure effectual production methods.

Collaborate with designers and engineering to ensure assemblies and components can be manufactured effectively.

Develop and write IQ/OQ/PQ protocols for appropriate equipment and systems within the guidelines of cGMP, internal policies and procedures.

Perform and/or supervise the execution of protocols.

Review executed protocols and write final reports.

Work closely with operations to develop, coordinate, and implement technical training for employees.

Create standard operating procedures (SOPs) for various validation related use.

Provide engineering support in operations to trouble shoot and resolve technical problems.

Support company policies and procedures, goals and objectives, all regulatory and GMP requirements.

QUALIFICATIONS

Manufacturing Engineer II

3-7 years experience in similar roles.

B.S. in Engineering (e.g. Manufacturing, Industrial, Mechanical) from an accredited college or university.

Prior experience in medical, biotechnology or similar field preferred.

Knowledge of manufacturing concepts and GMP.

Ability to grasp modern technology quickly.

Must be a strong communicator.

Ability to prioritize multiple projects.

Enthusiastic, cooperative, and positive behavior.

Lean Six Sigma experience - Green Belt preferred.





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, 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 his/her Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because he/she made a good faith report of discrimination.