Operations Specialist (3rd Shift)

West Point, PA, US
March 05 2018
Organization Type
Requisition ID: MAN004974

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 125-year legacy. 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.

The incumbent will:
  • Support the managers in 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 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 are properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
  • Participate in design and implementation of training and development programs.
  • 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 may require occasional weekend work due to the nature of biological processes

  • Bachelor’s Degree with emphasis in Science or Engineering
  • Minimum 2 years’ working experience in cGMP or equivalent environment (military, pharmaceutical, quality assurance, large manufacturing)Willing and able to work off-shift or weekends
  • Computer literacy in MS Office, Word, Outlook, Excel
  • Ability to identify and implement solutions for continuous improvement initiatives
  • Two or more years’ cGMP experience in a sterile, bulk, or finished pharmaceutical environment
  • Manufacturing plant experience in operational capacity
  • Experience working within a Union environment 
  • Experience with working in SAP or other Enterprise software
  • Technical writing experience 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 staffingaadar@merck.com.

 Search Firm Representatives Please Read Carefully: 

Merck 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

Job: Manuf./Operations Generic
Other Locations:
Employee Status: Regular
Travel: No
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck

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