Job Description
Job Description
The Analytical Research and Development Microbiology group has an opening for a Scientist - Microbiologist. 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 your role as Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data in a good manufacturing practices (GMP) microbiology laboratory, including finished products testing, utilities, and environmental monitoring. While working within a fast-paced, integrated, multidisciplinary team environment, the candidate is expected to have a strong working knowledge of microbiology laboratory practices and procedures in a GMP environment including microbiology data review and quality procedures. Prior Environmental Monitoring experience is a plus This position is based at the Rahway, New Jersey site.
**This position is a 2nd Shift schedule. **
Primary Responsibilities
- Perform routine viable and non‑viable Environmental Monitoring of classified cleanroom areas (Grad A-D), including surfaces, air, and equipment.
- Conduct active air, passive air (settle plates), surface sampling, in accordance with site EM programs and GMP requirements.
- Operate and maintain EM instruments (e.g., viable air samplers, particle counters, RODAC plates, isolator/BSC environmental sampling tools).
- Execute aseptic sampling techniques to ensure data integrity and contamination‑free sample collection.
- Perform utility sampling/testing (WFI, purified water, clean steam) and support routine water system monitoring.
- Perform microbiology laboratory testing associated with EM samples, including bioburden, microbial identification, and endotoxin testing.
- Trend, analyze, and interpret EM data; escalate atypical or out‑of‑trend (OOT) results and support investigations.
- Participate in deviation investigations, root cause assessments, and CAPA development related to environmental or microbiological events.
- Maintain accurate documentation of sampling activities in compliance with ALCOA and data‑integrity principles.
- Conduct microbiology finished goods testing and biological indicator (BIs) testing
- Support of sterile operations within the quality control department including utilizing isolator for sterility testing, conduct method suitability testing, endotoxin, microbial enumeration, media / reagent quality control testing, Experience with testing in clean room environments preferred
- Conduct the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA and data integrity principles
- Partner with internal stakeholders and partners, including Quality, Pipeline, and Operations.
- Perform second scientist review microbiology experiments in line with GMP expectations
- Support internal and external compliance audit activities.
- Conduct other job duties as per management assignments/business requirement.
- Be flexible weekday work hours and weekend support as needed
Education Minimum Requirements:
- BS Degree with 3+ years of pharmaceutical industry experience, with direct microbiological testing GMP experience.
- MS Degree with 2+ years of pharmaceutical industry experience, with direct microbiological testing GMP experience.
- Degree in Microbiology or related Biological Sciences, or equivalent.
Required Experience and Skills
- A proven record of microbiology laboratory experience.
- Excellent written and oral communication skills,
- Interpersonal skills, are necessary to qualify for this role.
- Knowledge and experience of microbiology testing in context of, environmental monitoring, aseptic manufacturing, and utilities testing in a GMP environment.
- Knowledge of current microbiology industry guidelines and compendiance.
Preferred Experience
- Knowledge in nonsterile and aseptic manufacturing.
- Associated GMP product testing.
- Experience in supporting quality investigations in the microbiology discipline.
- Experience with MODA, SAP, Veeva, LIMS is a plus.
#AR&D
**Required Skills: **
Adaptability, Data Integrity, Environmental Monitoring, Fast-Paced Environments, GMP Compliance, Laboratory Techniques, Microbiological Test, Standard Operating Procedure (SOP) Writing
**Preferred Skills: **
Adaptive Mindset, Interpersonal Relationships, OOS Investigations
Current Employees apply HERE
Current Contingent Workers apply HERE
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:
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
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
$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.
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:
No relocation
VISA Sponsorship:
No
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Not Applicable
Shift:
2nd - Evening
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
05/8/2026
***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. **