Merck & Co, Inc

Senior Scientist, Reagent Technical Development and Operations (On-site)

Merck & Co, Inc$117K — $184K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in analytical chemistry, molecular biology, cell biology, virology, or related field; or M.S. with 3 years of experience; or bachelor’s with 7 years of experience.
  • Demonstrated project management skills for large molecule portfolio projects.
  • Experience in monitoring reagent/assay performance and handling analytical bridging studies.
  • Proficient in independently collaborating in a team-centered environment.
  • Excellent verbal and written communication skills.

Responsibilities

  • Define, develop, and implement large molecule critical reagent strategies.
  • Oversee reagent qualification testing, documentation, and lifecycle management.
  • Manage both internal and external reagent development for the large molecule pipeline.
  • Collaborate with multidisciplinary teams to support biologics development.
  • Maintain detailed laboratory records.
  • Contribute to regulatory submissions and technical reports.

Benefits

  • Comprehensive medical, dental, vision healthcare and insurance benefits for employees and families.
  • Retirement benefits including 401(k).
  • Paid holidays, vacation, and sick days.
  • Flexible work arrangements where feasible.
Full Job Description

Job Description

The Large Molecule Analytical (LMA) Cell-Based Sciences Department is seeking a highly motivated Senior Scientist to join the Reagent Technical Development and Operations team in Cell-Based Sciences department in West Point, PA.  The qualified candidate will be responsible for developing critical reagent strategies for large molecules products across the biologics and vaccines pipeline. This senior scientist role will partner with cross-functional analytical development teams, regulatory and quality to deliver related Biological Critical Reagent strategies through the development lifecycle of a program.

The successful candidate is expected to provide scientific leadership, expertise, and creativity to solve complex project problems across the large molecule portfolio in developing critical reagents strategies.

 

Applicants must have effective organizational skills that enable support of multiple programs, have demonstrated excellent scientific expertise in analytical development, and have superior written and oral communications skills. The candidate will be expected to effectively communicate with stakeholders in partner organizations and with management and governance teams.

 

In this role, the Senior Scientist will:

  • Define, develop and implement large molecule critical reagent strategies.

  • Oversee and analyze reagent qualification testing, documentation, and lifecycle management.

  • Oversee both internally and externally sourced reagent development, production, and implementation to support the large molecule pipeline.

  • Collaborate with cross-functional teams to support biologics development.

  • Maintain accurate and detailed laboratory records.

  • Contribute to the preparation of regulatory submissions and technical reports.

Primary Responsibilities:

  • Develop Critical Reagent strategies for program specific reagents to support our Company's Research Laboratories Large Molecule Development portfolio.

  • Represent or provide technical oversight of team members on analytical and product development working groups. Collaborate effectively in a multidisciplinary team environment and provide technical input to enable team decisions.

  • Author and review critical reagent documents including reagent development reports, technical summaries, and reagent qualification protocols.

Education Requirements:

  • Ph.D. in analytical chemistry, molecular biology, cell biology, virology, or related field.

  • OR M.S. with a minimum of 3 years of relevant experience in Biopharmaceutical Industry.

  • OR bachelor’s with a minimum of 7 years of relevant experience in Biopharmaceutical Industry.

Required Skills and Experience:

  • Demonstrated project management skillset to oversee, prioritize, and deliver on critical reagents large molecule portfolio of projects.

  • Experience with monitoring reagent/ assay performance and control for drifts in key quality attributes between and within reference standards, and analytical bridging studies.

  • Demonstrated ability to work independently and collaborate effectively with cross-functionally in a team-based environment, partnering and influencing in a professional and effective manner.

  • Excellent verbal and written communications skills.

Please note that this lab-based role is not eligible for our hybrid work model, but we are committed to promoting work-life balance and offer other flexible arrangements where feasible.

#AR&D

EligibleforERP

Required Skills:

Analytical Chemistry, Analytical Method Development, Assay Development, Biochemical Assays, Biopharmaceutical Industry, Biopharmaceuticals, Cell-Based Assays, Immunoassays, Innovative Thinking, Molecular Microbiology, Project Management, Scientific Leadership, Stakeholder Communications, Strategic Thinking, Teamwork, Technical Writing

Preferred Skills:

Bioanalytical Analysis, Chromatographic Techniques, GMP Operations

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

The salary range for this role is

$117,000.00 - $184,200.00

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:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

08/18/2026

*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.

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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

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