Vendor Quality, Associate Director Job

Employer
Merck
Location
Gwynedd, PA, US
Posted
October 12 2017
Discipline
Other
Organization Type
Pharma
Requisition ID: QUA006346

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 is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 


With guidance from the vendor quality lead, contributes to the development of the vendor audit plan pertaining to quality oversight of clinical trial based vendor services. Communicates the overall quality strategy to research business areas including the identification and assessment of risk as it pertains to ongoing vendor compliance to operational standards and regulatory requirements. Formal risk assessment criteria is employed to aid in the selection of vendors for the annual audit plan and requires frequent consultation with the various research business areas as well as assimilating data on the vendor’s history of issues, current performance, and criticality of support provided to clinical trials. In addition, pro-active quality support is required through engagement on issues as part of vendor governance operational activities, serious quality issues investigations, and other venues where trends may be identified.  Suggestions for improved quality are communicated to both the research business and the supporting vendors.  Collaborates on quality issues information sharing and tasks with other research business quality functions to enable achievement of quality goals at the clinical trial protocol level. A detailed understanding of applicable regulations/guidances is required along with the ability to rapidly assess a vendor’s policies/procedures during audits and assessments. Vendor oversight methods and processes are employed in order to minimize and mitigate both operational and regulatory risks.  


Primary activities include but are not limited to :

  • Under the guidance of the vendor quality lead, provide support in the development of the MRL QA vendor audit plan pertaining to vendor services using formal risk assessment criteria aligned with MRL standards and regulatory requirements.  Engage with the research business areas to obtain appropriate input to the plan and ensure that research business areas understand the strategy. 
  • Independently implement the audit plan through execution of audit processes including audit scoping, audit conduct at vendor sites, and reporting of audit issues to MRL QA management and appropriate research business areas.  
  • Engage in follow up activities related to audit outcomes including additional audit reviews/assessments, meetings with the research business areas and/or vendors, and identification of audit outcome metrics to be reported to the MRL vendor management function.
  • Requires subject matter expertise (SME) in the application of GCPs to vendors providing functional and/or centralized services in the clinical trials.  Vendors may include functional service providers (FSP) for various clinical trial services (e.g. site monitoring, data management, biostatistics), laboratories, diagnostic testing (imaging, ECGs, polysomnography), and electronic clinical outcome assessments (eCOA).
  • Involves engagement with research business areas as part of formal operational governance forums, input on vendor quality agreements, consultation on vendor qualification processes and other ad hoc issues related to quality, and investigative interactions with other quality organizations in the research business areas.
  • Ability to evaluate vendor services for quality management systems, end-to-end operational data flow including data acquisition, data management, analysis, reporting, data transfers, and data reconciliation activities.
  • Build effective working relationships with key research business areas and vendor quality representatives. 
  • Engages with business quality groups to assimilate protocol level events and activities impacted by vendor performance as part of serious quality investigations, quality trending, and quality oversight. 
  • Conducts appropriate work in accordance with applicable and established Standard Operating Procedures (SOPs), applicable regulations, safety guidelines and company policies and procedures.
  • Contribute to the ongoing development of MRL QA operating standards, work instructions, and training materials to further develop competencies within the MRL QA Vendor group and any other MRL QA areas assisting in support of the vendor quality program.


Qualifications

Education:  

  • BS/BA in relevant area 

Required:  

  • A minimum of 10 years of experience in the pharmaceutical industry
  • A substantial work history in clinical trial activities/GCPs, QA oversight activities.


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 & 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.


For more information about personal rights under Equal Employment Opportunity, visit:

 

            EEOC Poster

            EEOC GINA Supplement 



Job: Quality Assurance
Other Locations:
Employee Status: Regular
Travel: Yes, 25 % of the Time
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck

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