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Director Quality

Requisition ID: QUA008427
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 Director will fill a key role in our manufacturing network and the selected candidate will be accountable for leading the quality organizations at two of the sites; providing strategic direction, coaching and support; driving results to meet the objectives of the sites and the company to ensure compliant supplies at competitive cost.
Additional responsibilities may include, but are not limited to:
Ensuring quality and compliance at the sites
Sponsor implementation of quality and compliance excellence
Supporting continuous improvement and efficiency improvements
Building talent and developing colleagues throughout the organization
Qualifications
Required Experience and Skills:
Bachelors in (Bio) Chemistry, Biologics or similar
Minimum 8 years' experience working in biological or pharmaceutical industry
Minimum 3 years' experience managing/leading a Quality/Manufacturing team/unit
Demonstrated continuous improvement skills
Ability to lead change, drive behavioral change and building talent/developing people
Strong analytical skills and the ability to think creatively.
Excellent leadership skills, along with the ability and willingness to work across organization.
Preferred Experience and Skills:
Master level degree in a Science/Business field
Experience working in a regulated environment (i.e. USDA, GMP)
Knowledgable in Lean concepts
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 assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to 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
OFCCP EEO Supplement
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of it's manifestations.
Job: Quality Operations
Other Locations: Omaha, NE, US
Employee Status: Regular
Travel: Yes, 5 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Hazardous Materials: common laboratory chemicals on rare occassions
Company Trade Name: Merck
Nearest Major Market: Omaha
Nearest Secondary Market: Council Bluffs


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