Scientist 3, Microbiology

Merck Group
Bedford, MA
Work Location: Bedford, Massachusetts
Shift:
Department: LS-PS-RVMM Microbiology
Hiring Manager: Alex Chalmers

This information is for internals only. Please do not share outside of the organization.

Your Role:

As a Scientist III in the Microbiological Sciences group, you will leverage your scientific and engineering expertise to develop, validate, and advance microbiological test systems that support product development and manufacturing within Process Solutions R&D. You will lead the design and implementation of robust bacterial ingress and retention testing methods, contribute to system automation initiatives, and collaborate cross-functionally to ensure scientific rigor, regulatory compliance, and product reliability. Your work will directly enable innovation in sterile filtration, contamination control, and microbial risk assessment-driving excellence in product quality, supply, and scientific leadership.
  • Develop and execute bacterial ingress and retention studies for filtration and single-use systems.
  • Design challenge models to evaluate system integrity and microbial barrier performance.
  • Author study protocols, analyze data, and prepare technical reports.
  • Collaborate with engineering and digitalization teams to automate bacterial retention testing systems.
  • Lead system integration projects to modernize microbial testing platforms across R&D and manufacturing labs.
  • Contribute to new equipment and test methods development aligned with regulatory standards (e.g., Annex 1, ASTM F838).
  • Plan and execute method development and validation studies for microbiological assays.
  • Support microbiological expertise in product/process changes, raw material qualification, and contamination control strategies.
Who You Are:

Minimum Qualifications:
  • Bachelor's degree in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline.
  • 5+ years of experience in microbiological method development, bacterial retention/ingress testing, or bioprocess system validation.
OR
  • Master's Degree in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline.
  • 3+ years of experience in microbiological method development, bacterial retention/ingress testing, or bioprocess system validation.
OR
  • PhD in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline.
Preferred Qualifications:
  • Experience in designing method development, bacterial retention/ingress testing, or bioprocess system validation.
  • Strong understanding of sterile filtration, contamination control, and regulatory standards (Annex 1, ASTM, PDA TRs, etc.).
  • Proficiency in data analysis, risk assessment, and technical documentation.
  • Excellent collaboration, communication, and problem-solving skills.
  • Experience with automated retention stands or development of custom bioprocess test rigs.
  • Familiarity with cleanroom practices, BSL-2 testing environments, and digital data acquisition systems.
  • Experience translating complex microbiological data into actionable design and process insights.
  • Hands-on experience with microbial challenge testing and aseptic system design.
Pay Range for this position: $110,000 to $135,000.

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here .

RSREMD

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
Posted 2026-01-17

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