Specialist, Engineering Deviation Management Job

Specialist, Engineering Deviation Management-CHE005155

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Specialist, Engineering is responsible for investigation support of formulation and filling of lyophilized products.

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Leads and/or works as a team member on manufacturing investigations and/or process improvement projects.

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Has ability to examine an issue from diverse perspectives (safety, compliance, automation, equipment, process, and people) in order to best understand and resolve the root cause.

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Assures consistent application of standardized work, engineering and process tools.

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Provides technical support to manufacturing shop floor for problems and issues.

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Conducts and designs experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale.

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Authors and updates technical and manufacturing documents necessary for investigations, process design/definition, engineering studies, process demonstrations, change control and validation

Qualifications

Education:

- B.S. degree in Engineering or Sciences. 　

Required Experience:

- Three (3) years post-bachelor’s degree experience in GMP manufacturing and/or technical support of GMP manufacturing operations (or M.S. degree plus 1 years; PhD degree plus 1 years).

- Highly developed communication, leadership and teamwork skills.　

- Strong Problem Solving Skillset

Preferred Experience:

- Vaccine formulation and filling

- Lyophilization 　

- Participation in Regulatory Inspections 　

- Sterile Processing

- Experience authoring investigations

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Chemical Engineering

Job Title:Spclst, Engineering

Primary Location: NA-US-PA-West Point

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: The responsibilities of this position require the employee to enter core sterile manufacturing areas.

Company Trade Name:Merck