Specialist, Analytical Instrument Validation (On-site)

Merck; Rahway (NJ); On-site; USD 96,000 - 151,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement

Paid holidays

Vacation

Sick days

Job summary

Merck & Co., Inc., Rahway, NJ, USA, is seeking an Analytical Instrument Validation Specialist to join the ECVC department in the Rahway research facilities. This role supports validation of novel computerized instrumentation in GMP environments across multiple sites, driving quality, compliance, and SDLC standardization.

The successful candidate will collaborate across DSCS, contribute to SOPs, investigations, and change management, and participate in digital innovation initiatives to improve

Qualifications

• Bachelor’s degree in analytical chemistry or related field with ≥3 years industry experience.
• Ability to work independently and cross-functionally within GMP environments.
• Excellent verbal and written communication and problem-solving skills.

Responsibilities

• Partner with scientific teams across DSCS to drive compliance.
• Validate novel instrumentation in GMP environments to 21CFR11.
• Support SDLC standardization across the network.
• Assist audits and maintain inspection readiness.
• Draft and contribute to SOPs.
• Own Investigations and Change Management records.
• Contribute to digital innovations for efficiency and compliance.

Skills

Team collaboration

Instrument validation

GMP knowledge

Communication skills

Education

Bachelor'sdegree in analytical chemistry or related field

Tools

Power Apps

Computerized systems

Job description

Job Description

The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our company Research Laboratories Division is seeking applicants for a Validation Specialist position available at either the Rahway, New Jersey research facilities.

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 environment for multiple sites (Pennsylvania, New Jersey, and Schachen, CH).

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.

Education Minimum Requirements (standard For Each Level)

Bachelor’s degree, or higher, in analytical chemistry 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
• 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

Preferred Experience And Skills

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
• Experience in Instrument commissioning, qualification, and validation (CQV)

AR&D

Adaptability, Adaptability, Analytical Chemistry, Analytical Instrumentation, Analytical Laboratory Equipment, Change Management, Code of Federal Regulations Title 21, Computer System Validation (CSV), Data Analysis, Diversity and Inclusion (D&I), Equipment Maintenance, Experimentation, GMP Compliance, GMP Environments, Inspection Readiness, Inventory Management, Metrology, Operational Excellence, Personal Initiative, Pharmaceutical Compliance, Regulatory Audits, Regulatory Compliance, Reviewing Literature, Standard Operating Procedure (SOP) Writing, Systems Development Lifecycle (SDLC) {+ 3 more}

Preferred Skills

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.

Requirements

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:

EEOC Know Your Rights

EEOC GINA Supplement

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

Salary Range

$96,200.00 - $151,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this 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.

Benefits

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.

Application Deadline

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

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

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.

Employee Status

Regular

Relocation

No relocation

VISA Sponsorship

No

Travel Requirements

25%

Flexible Work Arrangements

Not Applicable

Shift

1st - Day

Valid Driving License

No

Hazardous Material(s)

n/a

Job Posting End Date

09/5/2026

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.

Requisition ID

R395322