Laboratory Manager, Quality Control:
Merck

QUA006810-en_US
Merck
West Point Pennsylvania
Pharmaceutical
Description
Requisition ID: QUA006810

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. 


Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
Under the direction of the Associate Director, the Laboratory Operations Manager is responsible for enabling efficient execution of material testing for Merck’s Manufacturing Division in a safe and compliant manner, thereby contributing to the Merck’s ability to supply product to patients. 


The manager will take ownership of several analytical assays, including communication with laboratory technicians, product stakeholders and support groups. Specific duties may include the following:

  • Responsible for the activities involved in conducting testing of validation, raw material, process intermediates and finished product samples, and is knowledgeable in the analytical techniques for the laboratory(s) they support. 
  • Responsible for the supervision of hourly employees performing testing. Includes scheduling of work assignments based on priorities, being knowledgeable of cGMP, administration of local bargaining agreement, company personnel policies, OSHA requirements and company safety procedures. Promotes teamwork and open communication.
  • Act as a resource and liaison between technicians and support groups to represent the needs of the laboratory
  • Responsible for performing lab work accurately and in a timely fashion. Responsible for critically evaluating data generated and recommending acceptance or rejection of samples. 
  • Responsible for updating SOPs, Process Specific Training Modules, Test Methods, etc. 
  • Required to facilitate relationship with Quality Assurance group
  • Initiate and follow-up on equipment repairs and follow-up on facility work orders for laboratory modifications
  • Represent the laboratory in various Safety and Compliance initiatives, including safety inspections 
  • Maintain records, develop productivity improvement plans, maintain adequate inventory of supplies, training records, tracking functions such as corrective actions, special projects, etc.
  • Supports deviation investigations, out-of-trend results, and test failures associated with product manufacture, release testing, and stability testing.
  • Responsible to improve laboratory quality and/or efficiency of assays, support regulatory inspections and train other Laboratory Operations managers and/or technicians.

Qualifications

Education:

  • B.S/B.A. or M.S in Microbiology 

Required:
  • Minimum of (3) years’ post-degree laboratory, manufacturing, or quality control experience. 
  • Working knowledge of cGMPs
  • Deep familiarity of laboratory methods and common instrument requirements for a laboratory 
  • Must possess strong communication, project management and problem-solving skills
  • Demonstrated ability or aptitude for continuous learning and analytical problem solving. 

Preferred:
  • Customer service mentality and process improvement experience
  • MS in a science-related discipline

Note: Training may be required on 1st shift prior to transitioning to 2nd shift.

Your role at Merck isintegral to helping the world meet new breakthroughs that affect generations tocome, 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 FirmRepresentatives Please Read Carefully: 

Merck & Co., Inc. isnot accepting unsolicited assistance from search firms for this employmentopportunity.  Please, no phone calls or emails.  All resumessubmitted by search firms to any employee at Merck via email, the Internet orin any form and/or method without a valid written search agreement in place forthis position will be deemed the sole property of Merck.  No fee will bepaid in the event the candidate is hired by Merck as a result of the referralor through other means.

 

Visa sponsorship is notavailable for this position.

 

For more informationabout personal rights under Equal Employment Opportunity, visit:

 
            EEOC Poster

            EEOC GINASupplement 





Job: Quality Lab Related
Other Locations:
Employee Status: Regular
Travel:
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck
Basic Qualifications
Requirement