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Integrated Process Teams QA Support Millsboro, DE)


Millsboro, DE
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Job Details

Job Title: Integrated Process Teams QA Support Millsboro, DE)  - QUA006206


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. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. 



The quality IPT Support (Integrated Process Teams) lead will provide quality support to ensure manufacturing activities are in compliance with cGMP, regulatory, and legal requirements. This position reports to the Associate Director of Quality. Responsibilities include but are not limited to:

  • Collaborates with Manufacturing, Regulatory Affairs, EHS (Safety), R&D, BTS (Bioprocess Technology Support) and ATS (Analytical Technology Support) to ensure activities are within scope and ensure usage and implementation of quality knowledge, procedures, and guidelines.
  • Collaborates with site leadership on quality standards and best practices to ensure that all manufacturing processes are in compliance.
  •  Interacts with other Merck sites for best practice sharing.

Education Minimum Requirement:

Bachelor of Science degree in related science or engineering degree

Required Experience and Skills:
  • A minimum of 5 years industry experience in a biologics setting
  • Working knowledge of regulatory requirements in accordance with USDA manufacturing operations (9 CFR 113)
  • Proven project management skills
  • Excellent communication skills: able to communicate quality requirements as well as company and site strategies
  • Proficiency in computer systems and applications including but not limited to: Microsoft Office (Word, Excel and Outlook).
  • Ability to work independently and effectively with peers: display strong interpersonal and organizational skills

Preferred Experience and Skills:
  • cGMP experience



Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 


If you need an accommodation for the application process please email us at


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:




Job Quality GMP Related

Primary Location NA-US-DE-Millsboro

Other Locations 

Employee Status Regular

Number Of Openings 1

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