Manager, Operations (3rd Shift) Job

West Point, PA, US
September 08 2017
Organization Type
Manager, Operations (3rd Shift)-MAN004445


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.

This high impact role in Merck Manufacturing assures that products manufactured comply with cGMPs, operating procedures, and other applicable regulations.

Responsibilities include but are not limited to:

- Manage the direct processing of materials and the associated hourly workforce to ensure attainment of business results.
- Effectively collaborate with and manage a work team with specific responsibility for motivating others, ensuring performance, schedule execution, task coordination, equipment and area preparation and effective administration of personnel policies and procedures.
- Manage conflict and effect resolution to technical and personnel challenges is key as is openness to change and the ability to effect positive change.
- Because our business is dynamic and advances in science and technology require new methods of production we are looking for individuals who can do the following:
- Collaborate with team members in the identification and implementation of continuous improvement initiatives and action plans.
- Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence and lean practices.
- Demonstrate integrity, credibility and flexibility in their daily performance so as to motivate others to do the same.
- Assure compliance with safety and environmental practices, cGMPs and SOPs in the work area.
- Participate in external and internal audits and inspections.
- Initiate the investigation when a quality or safety event occurs during the shift.
- Work with members from Quality and Technical Services to properly handle unplanned events.
- Ensure that corrective actions are implemented.
- Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
- Participate in design and implementation of training and development programs.
- Perform performance management and disciplinary process.
- Ensure materials receiving and verification in the work area, equipment cleaning, set-up and area cleaning and verification are completed according to procedures.
- Assure that materials are properly handled and equipment is properly operated according to SOPs, guidelines, and regulations.
- Maintain control of processes and product quality by ensuring compliance with cGMPs, safety and environmental regulations.
- Monitor the manufacturing processes during the shift
- This position will be for the 3rd shift and may require weekends as well.



- Bachelor's Degree or higher in Science, Engineering or Business

- Minimum of two (2) years’ experience in cGMP or equivalent environment
- Willing and able to work off-shift or weekends
- Experience with Microsoft Office (Word, Outlook and Excel)
- Willing and able to focus on and obtain results
- Willing and able to effectively collaborate and manage a work team
- Willing and able to enact conflict resolution
- Willing and able to effectively respond to change
- Willing and able to identify and implement solutions for continuous improvement initiatives
- Leadership and interpersonal skills to motivate direct reports and peers toward the achievement of production goals.

- Two (2) years’ cGMP experience in a sterile, bulk, or finished pharmaceutical environment
- Two (2) years’ supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical)
- Manufacturing plant experience in an operational capacity
- Experience working within a Union environment
- Experience working in SAP or other Enterprise software
- Experience with technical writing related to investigations into manufacturing process variation

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

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opportunity. Please, no phone calls or
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method without a valid written search agreement in place for this position will
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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: Manuf./Operations Generic

Job Title:Mgr, Operations

Primary Location: NA-US-PA-West Point

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): 3rd

Company Trade Name:Merck

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