Specialist, Quality Control Execution Support (2nd Shift)

MSD Malaysia; West Point (PA); On-site; USD 87,000 - 137,000; Full time

Job summary

Merck seeks a Quality Control Execution Support Specialist to manage analytical method lifecycle, from transfer to validation and updates in QC operations.

You will support method qualification, investigations, and cross-functional reviews, while guiding site scientists and authoring regulatory documentation. This on-site role emphasizes collaboration and continuous improvement.

Qualifications

• Bachelor's or Master's in Chemistry, Biology, Microbiology or related field.
• 1+ year experience in analytical method introduction in biopharma/pharma.
• Experience with analytical methods (HPLC, cGE, ELISA, PCR, microbial methods).

Responsibilities

• Support new method introduction and tech transfer receiving lab support.
• Assess and implement changes for existing methods and equipment.
• Troubleshoot methods with cross-functional teams.
• Provide regulatory submission support and audits.
• Develop and own change controls for updates to analytical methods.
• Monitor lifecycle management of analytical methods.

Skills

Analytical Instrumentation

Analytical Method

GMP Compliance

Project Management

Communication Skills

Regulatory Submissions

Change Management

Education

Bachelor's degree in Chemistry/Biology/Microbiology

Master's degree in related field

Tools

HPLC

cGE

ELISA

PCR

Bioassays

Microbial Methods

Compendial Methods

Job description

Purpose of Role

The Quality Control Execution Support Specialist role (2nd shift) is responsible for supporting Analytical Procedure Life Cycle through end-to-end method lifecycle management including introduction of new analytical methods, act as the receiving unit for analytical transfers, SME assessment for all analytical method & equipment performance qualification, investigations, product testing and technical rationale. This work will support pipeline and commercial products by utilizing expertise in the analytical areas of separations, biochemistry, and microbiology.

Activities Within Role

Technical expertise to support:

• New method introduction (Direct to QC Validations /Tech Transfer Receiving Lab Support).
• New technology introduction.
• Assessment and implementation of changes for existing methods and equipment: Change in technical element of method e.g. Parameter change Change in equipment element of method e.g., column/reagent change.
• Method troubleshooting where cross-functional investigation is required.
• Technical SME for regulatory questions, audit support, reagent changes / supply issues to provided justification / rationale for analytical methods and equipment.
• Technical review of impact on Analytical methods and equipment as part of cross-functional team assessment of new/revised Global Test method / Compendia changes or updates.
• Analytical equipment troubleshooting.
• Initial training of end users in QC and Manufacturing and training of site analytical sciences personnel on lab systems, processes and methods where agreed.
• Investigation support for lab investigations.
• Authoring technical documentation in support of investigation and regulatory responses.
• Analytical impact assessors on all QC Lab OPS change controls.
• Technical Impact Assessment of proposed and finalized compendial changes.
• Development and ownership of change control for updates to analytical methods.
• Routine Assay Monitoring and lifecycle management of analytical methods.
• Supporting digital method development.

Continuous Improvements

Responsible for driving a culture of Continuous Improvement by deploying our Company Six Sigma tools Coaching and Training: The Analytical Sciences Team Lead will provide support, guidance, and expertise to ensure the success of the Analytical Sciences group; will model our Company Leadership behaviors and understand the MPS principles to drive a culture of continuous improvement building a High-Performance Organization.

Reports to

West Point Site Analytical Sciences, Quality Control Execution Lead

Behaviors, Job Experience and Qualifications

Key Behaviors

• Win as one team.
• Focus on what matters.
• Act with urgency.
• Experiment, learn and adapt.
• Embrace varied perspectives and inclusion.
• Speak Up and be open-minded

Required Education

• Bachelor's degree (1-3 years related work experience) or Master's degree (0 years related work experience) – in Chemistry, Biology, Microbiology or related field.

Required Experience & Skills

• 1+ years working on analytical method introduction and qualification within the biopharmaceutical and/or pharmaceutical industry.
• Experience with analytical methods (HPLC, cGE, ELISA, Bioassays, PCR, compendial methods, Microbial methods, cell-based assays)
• Flexible, self-motivated & ability to manage multiple priorities.
• Strong project management and stakeholder management skills required with demonstrated ability to influence across internal and external stakeholders.
• Proven ability to work as part of an interdependent team but also on own initiative to ensure progression of priorities.
• Experience in problem solving (facilitation & application of tools), risk management, decision making & trouble shooting skills.
• Excellent communication skills – verbal, written, presentations.
• Ability to coach and support development of AS&T Scientists and QC technicians within AS&T and QC teams.
• Provide leadership and expertise for preparation of regulatory submissions, inspection readiness, and support health authority inspections – including but not limited to interaction with inspectors, responding to observations and monitoring of commitments.

This role will require 5 day a week on site support for 2nd shift QC Laboratory Operations.

Required Skills

• Adaptability, Adaptability, Analytical Instrumentation, Analytical Method, Analytical Method Development, Analytical Thinking, Change Controls, Change Management, Coaching, Competency Development, Data Analysis, Decision Making, Dissolution Testing, Driving Continuous Improvement, ELISA Test, Equipment Implementation, GMP Compliance, Influencing Skills, Karl Fischer Titrations, Laboratory Documentation, Laboratory Reports, Laboratory Safety, Laboratory Testing, Method Improvement, Microbiological Analysis {+ 12 more}

Equal Employment Opportunity Employer

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

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

Salary Range

The salary range for this role is $87,300.00 - $137,400.00 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.

Location-based notices

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

Employee Status

Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Not Applicable Shift: 2nd - Evening Valid Driving License: No Hazardous Material(s): N/A

Job Posting End Date

10/7/2026

*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.

Company Overview

Our company 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 we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.