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Msat In Pharma Jobs (NOW HIRING)

... Pharma manufacturing systems. * Provide both technical and project management support as needed for CMC and packaging projects in the perimeter of MSAT in support of late stage NCE development, Life ...

Process Engineer 2

Redmond, WA ยท On-site

$80 - $100/hr

... MSAT Manufacturing Technology & Science on global/site objectives. * - Support non-conformance ... in pharma/biotech/life sciences, or an MS degree. * - Working knowledge of cGMP and regulatory ...

Sr. MSAT Development Engineer

Hygiene, CO ยท On-site

$100 - $125/hr

SUMMARY The Sr. MSAT Development Engineer provides technical leadership and documentation support ... In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in ...

MSAT Engineer I

Milford, MA ยท On-site

$60 - $80/hr

Select how often (in days) to receive an alert: Create Alert The role of the MSAT Engineer is to provide technical expertise of transfer of development processes into GMP manufacture. Working with ...

New

Pharma Senior Project Manager

Washington, VT ยท On-site

$196K - $224K/yr

STV currently has opening fora Pharma Senior Project Manager in the Construction Management group ... record in project management techniques, concepts, principles, and standardsfor MSAT, CQV ...

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Msat In Pharma information

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$41

$71

$120

How much do msat in pharma jobs pay per hour?

As of Sep 8, 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.

What does Msat in pharma do?

Msat in pharma typically refers to a Medical Science Associate, a role responsible for supporting medical and scientific communication, conducting clinical research, and ensuring compliance with industry regulations. They often collaborate with healthcare professionals, provide product information, and may assist in training or educational activities within pharmaceutical companies.
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Infographic showing various Msat In Pharma job openings in the United States as of September 2026, with employment types broken down into 5% Internship, 4% As Needed, 83% Full Time, 3% Part Time, 4% Contract, and 1% Nights. Highlights an 78% Physical, 3% Hybrid, and 19% Remote job distribution, with an average salary of $148,012 per year, or $71.2 per hour.

Process Engineer

Morristown, NJ โ€ข On-site

Contractor

Re-posted 24 days ago


Job description

Prefer Local

Responsibilities -

  • Support activities within MSAT-US regarding technical documentation, SOP's, and internal systems.
  • Development of technical positions regarding packaging and Pharma process, equipment, material and component performance and Regulatory compliance for *** packaging process practices. This includes investigating and recommending new packaging and Pharma processes, technologies, systems, and materials, for potential integration into *** packaging and Pharma manufacturing systems.
  • Provide both technical and project management support as needed for CMC and packaging projects in the perimeter of MSAT in support of late stage NCE development, Life Cycle Management Programs (LCM) and Commercial Products.
  • Support multi-functional teams to formulate plans and strategy that meets the defined objectives.
  • Collaborate with R&D Drug Development, iCMC, IA packaging sites, component, material and equipment suppliers, Regional Marketing, Regulatory, Supply Chain, and QA in the development of project strategies and objectives.
  • Lead or support the qualification (IOQ/PPQ) of process and packaging and primary and secondary equipment
  • Lead or support the qualification of transport systems for bulk / intermediates and finished products to established.

Qualifications

Bachelor's Degree/Undergraduate Degree or Advanced Degree in Process/Package engineering

If you are interested or have any references please share resume at mukul@brightmindsol.com.