Operations Manager:
Merck

MAN004804-en_US
Merck
West Point Pennsylvania
Pharmaceutical
Description
Requisition ID: MAN004804

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:
  • 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 rotate shifts based on Operational needs and will run 6:00 am to 6:00 pm.
Qualifications

Education:
  • Bachelor’s Degree or higher in Science or Engineering discipline
Required:
  • Minimum two (2) years’ working experience in cGMP or equivalent environment
  • Willingness to work off-shift or weekends
  • Computer literacy in MS Office, Word, Outlook, Excel
  • Ability to identify and implement solutions for continuous improvement initiatives
Preferred:
  • 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 operational capacity
  • Experience working within a Union environment Experience with working in SAP or other Enterprise software
  • Technical writing experience related to investigations in to manufacturing process variation

Your role at Merckis integral to helping the world meet new breakthroughs that affect generationsto come, and we’re counting on your skills and inventiveness to help makemeaningful contributions to global medical advancement. At Merck, we’reinventing for life.

 

If you need anaccommodation for the application process please email us at staffingaadar@merck.com.

 

Search Firm Representatives Please ReadCarefully: 

Merckis not accepting unsolicited assistance from search firms for this employmentopportunity.  Please, no phone calls oremails.  All resumes submitted by searchfirms to any employee at Merck via email, the Internet or in any form and/ormethod without a valid written search agreement in place for this position willbe deemed the sole property of Merck.  Nofee will be paid in the event the candidate is hired by Merck as a result ofthe referral or through other means.

 
Visa sponsorship is not available for this position.
 

For more information about personal rights under Equal EmploymentOpportunity, visit:



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