Onsite
Job Description
The role is on-site, based in Rahway, NJ and will support our second shift operations which operate from 3:00 PM EST to 11PM EST.
Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
In the role of Associate Principal Scientist, you will be a key member of the Analytical Research and Development Microbiology team, supporting a rapidly expanding pipeline through close collaboration with cross‑functional stakeholders. This role is responsible for generating and delivering critical microbiology data within a GMP laboratory setting, including finished product testing, utilities monitoring, and environmental monitoring.
Working within a fast‑paced, integrated, and multidisciplinary environment, the Associate Principal Scientist is expected to demonstrate strong proficiency in GMP microbiology laboratory practices, including microbiological data review, quality procedures, and compliance expectations.
In this role, you will be accountable for building and sustaining a scientifically sound, risk‑based, and inspection‑ready microbiology program by integrating Environmental Monitoring and Product Testing into a comprehensive contamination control strategy.
Primary Responsibilities
Lead the execution of microbiology finished product testing, utilities, and environmental monitoring in GMP environment
Leverage QC microbiology expertise as a subject matter expert in support of sterile operations within the quality control department including isolator qualifications, sterility testing, biological indicator challenge tests, and method suitability, endotoxin, microbial enumeration, media / reagent quality control testing, mycoplasma.
Directly contribute to experimental design of special studies in support of aseptic operations, execution, authoring and trend analysis of environmental monitoring and utilities trend reports.
Deep knowledge of risk-based assessment, Environmental Monitoring Performance Qualification (EMPQ), Clean Utilities Monitoring and contamination control strategies is essential. These skills ensure robust identification and mitigation of potential risks, as well as the implementation of comprehensive monitoring and preventive measures to maintain product integrity and regulatory compliance.
Experience with testing in clean room environments and Aseptic process validation preferred
Drive experimental design, execution, and data interpretation of microbiology data.
Oversee the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA and data integrity principle.
Execute test method suitability studies and implement microbiology methods to support release and stability testing of small molecule, biologic, and vaccines finished drug products.
Troubleshoot and lead any investigations associated with GMP testing through active collaboration with cross-functional project teams and/or Quality stakeholders. Identify appropriate corrective and preventative actions.
Partner with internal stakeholders and partners including Quality, Pipeline, and Operations.
Supervise microbiology testing, data entry, data review, equipment, lab inventory and author /approve reports and data summaries.
Conduct project management and/or scientific oversight of studies performed at Contract Laboratories
Contribute expertise and creativity to the collective knowledge and aid in solving complex problems.
Participate in internal and external compliance audit activities.
Perform additional duties as assigned.
Education Minimum Requirements
Minimum 4 years of pharmaceutical industry experience for applicants with a PhD degree; 10 years of experience with a MS degree, or 12 years of experience with a BS in Microbiology or related Biological Sciences, or equivalent with microbiological testing experience.
Required Experience and Skills
A proven record of strong technical problem solving and laboratory experience. Excellent written and oral communication skills, as well as interpersonal skills, are necessary to qualify for this role.
Extensive knowledge and experience of microbiology testing in context of, environmental monitoring program leadership – own and continuously improve the site EM program in alignment with EU GMP Annex 1and internal standards
Design and justify risk- based EM strategies ( locations, Frequencies, methods) and ensure integration of EM into the Contamination Control Strategy (CCS)
Oversee EM lifecycle activities, including EMPQ, requalification and periodic review
Lead EM data trending and statistical evaluation( e.g. MODA or equivalent systems
Identify emerging risk, low- level trends, and adverse patterns
Extensive knowledge and experience of microbiology testing in aseptic manufacturing, and finished product testing in a GMP environment
Translate microbiological data into proactive risk mitigation actions
Expertise in nonsterile and aseptic manufacturing and associated GMP product testing
Experience in leading and supporting quality investigations in the microbiology discipline
Experience with internal / external audit process and authoring responses to observations
Knowledge of current microbiology industry guidelines and compendia
Experience with MODA, SAP, Veeva, LIMS is a plus.
Leadership
Demonstrated ability to mentor, guide, and develop laboratory staff, fostering a collaborative and high-performance work environment.
Proven experience in managing cross-functional teams and coordinating microbiology projects to meet deadlines and quality standards and ensuring teams meet timelines / deliverables.
Strong decision-making skills and the capacity to lead by example, ensuring compliance with regulatory requirements and company policies.
This role is responsible for building and sustaining a scientifically robust, risk based, and inspection ready microbiology program, integrating Environmental Monitoring and Product Testing into a comprehensive contamination control strategy.
Required Skills:
Adaptability, Biological Sciences, Environmental Monitoring, GMP Compliance, Good Manufacturing Practices (GMP), Laboratory Information Management System (LIMS), Laboratory Techniques, Scientific leadership, Microbiological Tests, Aseptic techniques, Standard Operating Procedure (SOP). Interpersonal Relationship, Self-Motivation, Problem Solving, Communications, and Team Player.
#AR&D
Required Skills:
Adaptability, Adaptability, Analytical Method Development, Assay Development, Biological Assay Development, Biological Sciences, Biomedical Sciences, Cell-Based Assays, Chromatographic Techniques, Contamination Control, Cross-Functional Teamwork, Environmental Monitoring, External Collaboration, GMP Compliance, Good Manufacturing Practices (GMP), High Resolution Mass Spectrometry (HRMS), Laboratory Information Management System (LIMS), Laboratory Techniques, Liquid Chromatography-Mass Spectrometry (LC-MS), Manufacturing Compliance, Mass Spectrometry Analysis, Microbiological Test, Optimism, Problem Solving, Process Analytical Technology (PAT) {+ 2 more}Preferred Skills:
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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.
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U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
The salary range for this role is
$142,400.00 - $224,100.00This 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:
RegularRelocation:
DomesticVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
Not ApplicableShift:
2nd - EveningValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
05/29/2026*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.
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