Merck & Co, Inc

Senior Specialist, Quality Control

Merck & Co, Inc • $106K — $167K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemistry, Biology, or Engineering
  • 4+ years in a pharmaceutical laboratory setting
  • Proficient in Empower chromatography software, ideally in a coordinator role
  • Experience with CMMS systems, preferably SAP or EAM
  • Knowledge of GMP and government regulations
  • Familiarity with analytical instrumentation (HPLC, GC, etc.)

Responsibilities

  • Prepare and maintain documentation for maintenance jobs
  • Coordinate calibration programs and maintenance planning
  • Analyze equipment and preventive maintenance effectiveness
  • Serve as Empower CDS coordinator for site data management
  • Lead problem-solving initiatives to enhance equipment reliability
  • Manage vendor relations and support service reviews
  • Participate in quality investigations and audits

Benefits

  • Medical, dental, and vision healthcare for employees and families
  • Retirement benefits including 401(k)
  • Paid holidays and vacation days
  • Compassionate and sick leave
  • Comprehensive benefits package available
Full Job Description

Job Description

The Technical Support Senior Specialist is responsible for advanced preparation of maintenance jobs; responsible for maintaining instrumentation, equipment, and associated data, preventive maintenance data and calibration data; processes change control for equipment and preventive maintenance documentation, coordinates calibration program, coordinates maintenance planning operations within the laboratory for consistency, plans and schedules maintenance work orders, schedules PM's, maintains equipment histories, analyzes equipment & preventive maintenance effectiveness, and tracks maintenance metrics. 

 

They demonstrate mastery of analytical and maintenance management programs (SAP, EAM, GLIMS, Empower, eShopFloor, LabX, etc.).  Maintain positive vendor relations and support review/completion of vendor services.  Assures compliance with FDA & GMP regulations.  Is a recognized resource to others and demonstrates the ability to influence a team in the efforts to manage routine and project-based work. Provides input in the management of equipment related budget planning. Implements cost saving initiatives. Uses vast experience in analytical equipment and programs for troubleshooting and implementation of process improvement ideas.

 

A core function for this role will be to serve as the site's Empower CDS coordinator. This entails validation and maintenance of site mater data including custom fields, reports, instrument methods, sample sets and method sets in accordance with global procedures and applicable pharmacopeia. The Empower coordinator is expected to collaborate with DLR and GLIMS teams on creation and management of digital methods.

 

This position is being posted with an expected start date of January 2027.

 

Key Functions

 

Development

Work Independently and as a Team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect | Inclusion

Participate in development of objectives and ensures alignment with site goals

Laboratory Support

  • Initiating/leading problem solving to identify short-term and long-term actions to prevent problem reoccurrence, reduce laboratory downtime and increase equipment reliability
  • Following standard work for escalation as it related to safety, quality and downtime events
  • Timely approval of qualification, change control, procedures and other documents
  • Providing operational Subject Matter Expert support/direction for the installation of new equipment and/or modifications to existing processes and/or equipment
  • Demonstrates a deep understanding of customer needs, requirements, and expectations.
  • Pays close attention equipment use/maintenance and proactively steps in to help as needed.
  • Maintains equipment preventative maintenance/calibration programs
  • Independently manages equipment procurement, validation and qualification
  • Manage and participate in analytical Method Transfer activities

Information Transfer

  • Attends departmental and team meetings focused on equipment/process improvement
  • Serves as liaison between NASU teams, Leadership, Global network, and External Vendors
  • Ability to interpret company Quality Policies and Guidelines for daily application.
  • Participates and/or directs Tier meetings
  • Promotes teamwork and open discussion of issues.

Compliance

  • Uses Root Cause Analysis tools to identify true root cause for quality and safety events
  • Authors, reviews, approves and/or participates in quality investigations
  • Familiarity of compendial requirements and their application to laboratory testing and equipment
  • Participates in internal and external audits and inspections
  • Identifies equipment-related trends and facilitates implementation of corrective actions
  • Creates/Revises Standard Operating Procedures, Forms and other equipment-related documents
  • Understands and applies regulatory / compliance requirements, including GMP, NDA, and related regulations, and can interpret those regulations for implementation in the workplace.
  • Acts as a QMS Topic Owner and/or supports QMS updates
  • Manage and perform periodic review for access and orphan data in systems such as LabX, Empower, eShopFloor
  • Authors, owns, approves SOPs, Change Requests and other technical documents
  • Manage and perform equipment periodic review to verify performance of instrumentation and equipment 

 

Minimum Education Requirements

  • Bachelor of Science degree, preferably in Chemistry, Biology, or Engineering

 

Required Experience and Skills

  • ≥ 4 years in a pharmaceutical laboratory setting
  • High level of proficiency with Empower chromatography software, preferably with experience in a coordinator role
  • Knowledge and experience of CMMS systems is essential, ideally SAP or EAM
  • Experience managing vendors and contractors
  • Working knowledge of cycle time and inventory management, GMP's, Government regulations
  • Experience with analytical instrumentation (HPLC, GC, Dissolution, KF, etc.)

Required Skills:

Adaptability, Adaptability, Analytical Instrumentation, Analytical Method Development, Analytical Thinking, Calibration Procedures, Change Controls, Decision Making, Detail-Oriented, Equipment Calibrations, Equipment Implementation, Equipment Maintenance, Equipment Management, Equipment Monitoring, Equipment Qualification, Forensic Chemistry, Goal Setting, Good Manufacturing Practices (GMP), Government Regulation, Laboratory Information Management System (LIMS), Laboratory Operations, Management Review, Procedure Reviews, Quality Standards, Regulatory Audits {+ 8 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

The salary range for this role is

$106,200.00 - $167,200.00

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.

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.

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:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

NA

Job Posting End Date:

10/13/2026

*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.

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

Merck & Co, Inc Careers

Join the visionary team at Merck & Co, Inc, a global leader in healthcare dedicated to advancing the world of medicine. As part of our professional community, you'll find dynamic job opportunities that foster innovation and leadership across various fields. Merck & Co, Inc is not just a company; it's a place where you can make a difference.

Work You’ll Do

At Merck & Co, Inc, we are committed to improving global health through groundbreaking research and innovative healthcare solutions. Our team is at the forefront of developing new therapies and vaccines that significantly impact public health worldwide. By joining us, you will collaborate with some of the brightest minds in the industry, using your skills to contribute to projects that save and improve lives around the globe.

Explore Career Paths

Whether you're seeking an internship, a graduate opportunity, or a professional position, Merck & Co, Inc offers a range of career paths in environments that promote rapid professional growth and development. Explore job opportunities in research, digital transformation, manufacturing, and more, all while benefiting from a culture that supports diversity and inclusion.

Innovate and Lead

Merck & Co, Inc is an ideal environment for those who lead with curiosity and the drive to innovate. Our leadership is committed to fostering a culture where inventive thinking and collaboration are encouraged, making it a perfect place for professionals who seek to make an impact through their work.

Develop Your Skills

With Merck & Co, Inc, you are not just getting a job; you're gaining access to unparalleled career development opportunities. Enhance your skills through diverse training programs, workshops, and continuous learning courses designed to help you grow at every stage of your career.

Benefits and Culture

We understand that our employees are our greatest asset, which is why we offer competitive benefits designed to support the health and well-being of you and your family. From comprehensive health care coverage and retirement plans to flexible working conditions and wellness programs, our benefits package is designed to meet the diverse needs of our team members.

Join Our Team

Ready to advance your career at Merck & Co, Inc? Search open positions that match your skills and interests. We are continuously hiring and looking for passionate, creative, and solution-driven team players. Prepare your resume, sharpen your interview skills, and become part of a company that's dedicated to making a difference.

Stay Connected

Keep up to date with career tips, insider perspectives, and industry-leading insights you can put to use today—all from the people who work here. Engage with us through our careers blog and by participating in networking events and employment fairs. Subscribe to receive personalized job alerts and the latest news tailored to your preferences. Discover the exciting and rewarding opportunities that await at Merck & Co, Inc. Join us in our mission to improve health and wellness around the world.
Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ

Similar Jobs

More Jobs at Merck & Co, Inc

More Pharmaceuticals & Biotech Jobs

Find similar Senior Specialist, Quality Control jobs: