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Msat In Pharma Jobs (NOW HIRING)

Fujifilm

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

Cross-Functional Collaboration - partners with Manufacturing and MSAT/Engineering on facility ... in cGMP pharma/biotech or sterile medical device manufacturing, including environmental/utility ...

Cellares

Senior Process Engineer

Bridgewater, NJ

$90K - $210K/yr

Work as the MSAT representative on client projects * Lead activities to transfer processes to ... Experience in the Pharma/Biotech industry in technology transfer * Must know and follow job safety ...

Cellares

Process Engineer

South San Francisco, CA

$90K - $210K/yr

Work as the MSAT Process Engineer on internal or client projects * Responsible for technology ... Experience in the Pharma/Biotech industry in technology transfer * Must know and follow job safety ...

Cellares

Senior Process Engineer

South San Francisco, CA

$90K - $210K/yr

Work as the Senior MSAT Process Engineer on client projects * Responsible for technology transfer ... Experience in the Pharma/Biotech industry in technology transfer * Must know and follow job safety ...

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$125K - $161K/yr

Work as the Senior MSAT Process Engineer on client projects * Responsible for technology transfer ... Experience in the Pharma/Biotech industry in technology transfer * Must know and follow job safety ...

Cellares

Process Engineer

South San Francisco, CA

Work as the MSAT Process Engineer on internal or client projects * Responsible for technology ... Experience in the Pharma/Biotech industry in technology transfer * Must know and follow job safety ...

FUJIFILM Biotechnologies

$22 - $29/hr

... MSAT/Engineering, QA/QC, EHS) to maintain product quality and patient safety. This role exists to ... in cGMP pharma/biotech or sterile medical device manufacturing, including environmental/utility ...

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How much do msat in pharma jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for msat in pharma in the United States is $71.16, according to ZipRecruiter salary data. Most workers in this role earn between $53.12 and $79.09 per hour, depending on experience, location, and employer.

What is the difference between Msat In Pharma vs Clinical Research Associate?

AspectMsat In PharmaClinical Research Associate
Required CredentialsBachelor's degree, often with certifications in clinical trials or pharmaceutical sciencesBachelor's degree, often with certifications in clinical research or Good Clinical Practice (GCP)
Work EnvironmentPharmaceutical companies, biotech firms, or contract research organizations (CROs)Clinical trial sites, hospitals, or research organizations
Employer & Industry UsagePrimarily in pharmaceutical and biotech industriesIn clinical trial management and monitoring

Msat In Pharma and Clinical Research Associate roles share similar educational backgrounds and certifications, often working within the pharmaceutical industry. While Msat In Pharma focuses on supporting clinical trial processes within pharmaceutical companies, Clinical Research Associates primarily monitor and manage clinical trial sites. Both roles are essential in drug development, but their work environments and specific responsibilities differ slightly.

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Msat In Pharma jobs near you
Infographic showing various Msat In Pharma job openings in the United States as of August 2026, with employment types broken down into 69% Full Time, 5% Part Time, 21% Contract, and 5% Nights. Highlights an 100% In-person job distribution, with an average salary of $148,012 per year, or $71.2 per hour.

Senior QC Microbiologist

Fujifilm

Holly Springs, NC • On-site

$22 - $29/hr

Other

Re-posted 18 days ago

Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 68 frontline employees who took The Breakroom Quiz

50th of 540 rated manufacturers

Job description

Position Overview
The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial contamination across facilities, utilities, processes, and products. The roleapplies microbiology principles to validate sterilization, aseptic processing, and cleaning/sanitization; executes environmental and utility monitoring; and ensures compliance with FDA, EU, and global regulatory requirements. This position leads complex testing and data analysis, investigates contamination events and deviations, and partners cross-functionally (Manufacturing, MSAT/Engineering, QA/QC, EHS) to maintain product quality and patient safety. This role exists to ensure microbiological control, robust validation, and data-driven decision-making throughout the product lifecycle.
Company Overview
FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.
We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers
Job Description
  • Monitoring and trending - trend monitoring of cleanrooms (air, surfaces, personnel), utilities (WFI/PW, clean steam, compressed gases), and materials for microbial contamination using compendial and rapid methods; ensure timely data review and alert/action response. This includes authoring trending reports and organisms' evaluation.
  • Process support - authors/executes protocols and reports for sterilization (SIP/terminal), aseptic process simulations (media fills), cleaning and sanitization validation, and disinfectant efficacy studies; align with Annex 1 and applicable standards.
  • Investigations and CAPA - leads or supports investigations for deviations, OOS/OOT, EM excursions, and contamination events; perform root cause analysis (e.g., fishbone, 5-Whys, FMEA); define and implement effective CAPAs and effectiveness checks.
  • Data, Metrics, and Reporting - performs statistical analysis and trending; maintain LIMS/QMS records; generate dashboards (EM performance, utilities, sterility assurance KPIs), and present to site governance for data-driven decisions.
  • Method Development/Validation - implements and validates compendial and rapid microbiological methods (e.g., bioburden, endotoxin/LAL, sterility, microbial ID via MALDI-TOF/16S, qPCR, ATP bioluminescence); perform change controls and tech transfers.
  • Training and Coaching - develops and delivers training for operators and site staff on aseptic technique, gowning, EM practices, and contamination control behaviors; perform qualification and requalification assessments
  • Cross-Functional Collaboration - partners with Manufacturing and MSAT/Engineering on facility design and improvements; support GEMBAs and change management.'
  • Audit/Inspection Readiness - supports internal audits and regulatory inspections; remediate findings; maintain inspection-ready documentation and areas.
  • Performs and Exercises independent judgment to respond to EM excursions, water alerts, and in-process contamination signals; escalates per SOP and CCS.
  • Interprets regulations and standards to recommend controls and CAPAs; selects appropriate test methods and sampling strategies within approved procedures.
  • Decisions typically involve moderate to complex issues with significant quality impact; consults with QA and site leadership for batch-impacting decisions.
  • Perform other duties as assigned.

Minimum Requirements:
  • Bachelor's degree in chemistry, Biochemistry, Microbiology or other relevant scientific discipline with 8+ years' experience OR
  • Master's degree in chemistry, Biochemistry, Microbiology or other relevant scientific discipline with 6+ years' experience OR
  • PhD with 4+ years of applicable industry experience; 8 years of relevant microbiology experience in cGMP pharma/biotech or sterile medical device manufacturing, including environmental/utility monitoring, aseptic processing, and contamination control.
  • Hands-on experience with compendial methods (USP/EP/JP), endotoxin testing (LAL), bioburden, sterility testing, EM, and microbial identification.
  • Experience supporting or executing validation for sterilization, aseptic processing (media fills), and cleaning/sanitization.

Preferred Requirements:
  • Experience with rapid microbiological methods (e.g., PCR/qPCR,ATP), LIMS and eQMS systems, and statistical tools (e.g.,Minitab/JMP).

EEO Information
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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About Fujifilm

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With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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