New · posted Oct 16
Merck · Pharmaceuticals
Specialist, Global Analytical Instrument Validation
- West Point, PA
- On-site
- Full-time
- Associate & Specialist
Closes Oct 29, 2026 · 14 days left
The role
Specialist, Global Analytical Instrument Validation Specialist, Pharmaceutical Analysis & Digital Technologies
The Pharmaceutical Analysis & Digital Technologies (PADT) Analytical Capabilities and Operations (ACO) department of our Research & Development Division is seeking applicants for a Validation Specialist position available at the West Point research facility.
The Analytical Instrument Validation Specialist will work as part of the integrated Validation and Compliance team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The Analytical Instrument Validation Specialist role oversees and/or supports the validation of novel computerized analytical instrumentation within the GMP laboratory environment for multiple sites (Pennsylvania, New Jersey, and Schachen, CH).
What you need
Education Minimum Requirements
- Bachelor’s degree, or higher, in analytical science, information technology or related field with 3+ years post-degree relevant industry experience.
Required Experience and Skills
- A strong team player with the ability to work both independently and cross-functionally to deliver on complex objectives.
- Proven track record of strong technical and innovative problem solving.
- Desire and ability to learn new concepts outside of core expertise and training, including applications of/for Artificial Intelligence (AI).
- Excellent verbal and written communication skills, demonstrated creativity, and strong interpersonal skills.
- Related industry experience with computerized equipment or instrument validation.
- Experience working within a GMP environment.
- Understanding of GMP policies and procedures.
While not required, experience in one or more of the following areas is beneficial
- Demonstrated commitment to diversity and inclusion.
- Experience with IT, computerized systems, software and applications, including Secure Desktop.
- Experience with developing tools (e.g., Power Apps) or utilizing AI. Experience leading a team for a common goal.
- Experience in Auditing and Compliance within pharmaceutical industry, including change management and deviation management.
- Experience supporting internal and external quality audits.
- Experience in instrument computer system validation.
EligibleforERP
Required Skills
Analytical Instrumentation, Analytical Laboratory Equipment, Computer System Validation (CSV), Data Analysis, Equipment Maintenance, Experimentation, GMP Environments, GMP Laboratory, Inventory Management, Regulatory Compliance, Standard Operating Procedure (SOP) Writing, Technical Writing
Travel Requirements
25%
What you'll do
The key responsibilities of this role will include
- Partner with scientific teams across DSCS to drive compliance and operational excellence.
- Validate novel and time-sensitive instrumentation in GMP environments to 21CFR11 compliance.
- Support standardization activities for System Development Life Cycle globally.
- Support internal quality and external regulatory audits and maintain laboratory state of permanent inspection readiness within the scope of SDLC.
- Contribute to Standard Operating Procedures (SOP) drafting.
- Originate and own Investigations and Change Management records.
- Contribute to digital innovation activities supporting operational excellence for improved consistency, compliance, and efficiency.
The successful candidate must function both independently and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. Strong communications skills and eagerness to adapt and learn are essential attributes. As a member of our team, you will be joining scientific and technical problem solvers who are dedicated to creating the life-changing medicines of tomorrow.
Pay and benefits
$96,000 – $151,000 a year
Employer providedAdditional location(s) Compensation Information
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
Medical, dental and vision insurance
401(k) retirement benefits
Paid holidays
Vacation
Sick days
Annual bonus and long-term incentive
Where you'll work
West Point, PAOn-siteOpen in Maps (opens in a new tab)
More jobs in West Point, PAWorking conditions
1st - Day
Hazardous Material(s)
n/a
Employee Status
Regular
Relocation
No relocation
VISA Sponsorship
No
Flexible Work Arrangements
Not Applicable
Job Posting End Date
10/29/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Equal opportunity, accessibility and legal noticesMerck's statements, word for word
US and Puerto Rico Residents Only
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
The primary location for this posting is:
USA - Pennsylvania - West Point
Where required by law, the compensation range for this role is provided below.
The salary range for the primary location of this role is:
$96,200.00 - $151,400.00
This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Job intelligence
The context around this role
Live data · October 16, 2026
Salary intelligence
How the pay compares
This role's midpoint is 60% above the US median for Validation & CQV roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US21 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $96,000 | — | $151,000 |
| All US (middle half) | $77,000 | $77,000 | $92,000 |
This role: Merck's own published range. Comparisons: the base pay employers published on open Validation & CQV roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Validation & CQV
The general path across 117 open Validation & CQV roles on Regulatory Jobs, with the titles they carry most. Not Merck's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance10
- Lab testing and methods9
- Validation and qualification7
- Collaboration and leadership7
- Documentation and SOPs5
- Data and digital systems5
- Investigations and CAPA2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Merck on Regulatory Jobs
- 20
- Open roles
- 20
- Distinct roles
- 5
- Locations
By discipline
- Regulatory11 55%
- Quality8 40%
- Compliance & Safety1 5%
By level
- Director8 40%
- Senior & Principal6 30%
- Associate & Specialist6 30%
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Specialist, Global Analytical Instrument Validation at Merck
Applications close October 29. $96K–$151K a year, employer provided.