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Senior Technical Analyst Lab System Validation

West Point, PA

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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
As a Lab System Validation Senior Technical Analyst, you will ensure instrumentation critical to our regulatory compliance processes can be properly released for use in priority research workflows. You be joining a growing team of staff dedicated to pursuit of excellence in pharmaceutical research within Global Lab Computing supporting research projects.
 You will:
Promote strong partnership with scientists and local support teams
Ensure a high touch IT support (focused on engagement and outcome) to enhance research workflows and capabilities
collaborate with Quality Assurrance, IT and business areas ensure SDLC compliance
partner with core IT functions to enable consistent high quality support for all IT activities
contribute to the continuous improvement of SDLC processes and documentation Best Practices
manage outsourced Technical Writers in support of GxP documentation required for regulated laboratories
Education Minimum Requirement:
Bachelor’s degree (preferable disciplines: Pharmaceutical Sciences development related, Information Technology)
Required Experience and Skills:
Minimum 5 years of experience in Pharmaceutical/Biotechnology industry
Knowledge and experience in System Development Lifecycle (SDLC)
Knowledge and technical expertise in GMP and GLP requirements
Experience in technical writing and review of GMP/GLP documentation
Competency in leading development and change management initiatives in a matrix environment
Ability to work with service vendors and other IT groups to address business needs through innovative solutions
Managed operational aspects for IT team including budget, third party vendors
Detail oriented, thorough, well organized and effectively manage time
Strong communication and interpersonal skills
Preferred Experience and Skills:
Advanced level of knowledge relative to technical expertise and GMP/GLP requirements as it relates to Merck SDLC
Ability to leverage global functions to drive resolution of broad and technical issues
Led efforts to streamline and improve existing services
Design, construction, configuration and installation of IT solutions
Demonstrated success with business adoption and value realization
Independently prioritizes activities in support of multiple projects
Effective project planning ability to own and lead all technical deliverables working in collaboration with a Program/Project Manager
Excellent business acumen for managing & prioritizing demand, and demonstrated delivery of business value
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 assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to
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.
Visa sponsorship is not available for this position.
For more information about personal rights under Equal Employment Opportunity, visit:
            EEOC Poster
            EEOC GINA Supplement
Service Delivery/Management
Other Locations:
Kenilworth, NJ, US
Employee Status:
Yes, 10 % of the Time
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name:
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