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Ms&T Pharma Jobs (NOW HIRING)

Unicon Pharma Inc.

Supply Chain Specialist I

Edison, NJ · On-site

$42 - $50/hr

This includes New Product Introduction, R&D, and MS&T requirements, along with all Inline ... Experience in pharma industry with manufacturing and packaging, especially Oral Solid Dosage forms ...

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How much do ms&t pharma jobs pay per year?

As of Aug 9, 2026, the average yearly pay for ms&t pharma in the United States is $393,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $400,000.00 and $400,000.00 per year, depending on experience, location, and employer.

What are MS&T roles in the pharmaceutical industry?

MS&T stands for Manufacturing Science and Technology, a department in the pharmaceutical industry responsible for supporting the transfer, scale-up, validation, and optimization of manufacturing processes. MS&T professionals bridge the gap between research and commercial production by ensuring that products are made consistently, safely, and in compliance with regulatory standards. Their work includes troubleshooting manufacturing issues, implementing process improvements, and supporting technology transfers to production sites. MS&T teams play a critical role in ensuring product quality and regulatory compliance throughout a drug's lifecycle.

What is the difference between Ms&T Pharma vs Pharmaceutical Sales Representative?

AspectMs&T PharmaPharmaceutical Sales Representative
Required CredentialsDegree in pharmacy, life sciences, or related field; certifications in pharmaceutical salesHigh school diploma or bachelor's; often requires sales or healthcare knowledge
Work EnvironmentPharmaceutical companies, labs, or manufacturing facilitiesHospitals, clinics, pharmacies, and healthcare settings
Employer & Industry UsagePrimarily in pharmaceutical manufacturing and research companiesIn pharmaceutical companies, focusing on product promotion and sales

Ms&T Pharma roles typically involve research, development, and manufacturing within pharmaceutical companies, requiring scientific credentials. In contrast, Pharmaceutical Sales Representatives focus on promoting and selling products to healthcare providers, often working in sales environments. Both roles are integral to the pharmaceutical industry but differ in responsibilities and work settings.

How does an MS&T professional in pharma typically collaborate with cross-functional teams during process transfers or scale-ups?

MS&T professionals in the pharmaceutical industry play a key role in bridging the gap between process development, manufacturing, and quality teams, especially during process transfers or scale-ups. They work closely with R&D scientists, production engineers, quality assurance, and regulatory affairs to ensure smooth technology transfer, troubleshoot issues, and maintain compliance with GMP standards. Effective communication and project management skills are essential, as MS&T professionals often coordinate meetings, prepare technical documentation, and lead investigations to optimize processes. This collaborative environment offers valuable exposure to multiple departments and can open pathways to broader leadership or technical roles.

What are the key skills and qualifications needed to thrive as an MS&T professional in the pharmaceutical industry, and why are they important?

To thrive as an MS&T Pharma professional, you need a strong background in pharmaceutical sciences, engineering, or a related field, with expertise in process development and validation. Familiarity with technical tools such as process analytical technology (PAT), statistical analysis software, and knowledge of regulatory systems like GMP and FDA guidelines is crucial. Excellent problem-solving abilities, communication, and cross-functional teamwork set candidates apart in this role. These skills ensure robust process optimization, regulatory compliance, and successful technology transfer, all of which are vital for efficient and safe pharmaceutical manufacturing.
What job categories do people searching Ms&T Pharma jobs look for? The top searched job categories for Ms&T Pharma jobs are:
Ms T Pharma jobs near you
Infographic showing various Ms&T Pharma job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $393,215 per year, or $189 per hour.

Deviation Writer

Stark Pharma Solutions Inc

Bloomington, IN • On-site

Contractor

Re-posted 29 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Deviation Writer

Location: Indiana (Onsite)

Duration: 6-Month Contract

Position Overview:

We are seeking an experienced Deviation Writer to support Manufacturing Engineering and Quality Operations within a GMP-regulated pharmaceutical or biotechnology environment. This role will be responsible for authoring high-quality deviation investigations, performing root cause analysis, and collaborating with cross-functional teams to ensure timely and compliant resolution of quality events.

The ideal candidate will have strong technical writing skills, experience in deviation management, and the ability to translate complex manufacturing and engineering issues into clear, data-driven investigations.

Key Responsibilities

  • Author, review, and manage deviation investigations within a GMP-regulated environment.
  • Collaborate with Manufacturing, Production Engineering, MS&T, Supply Chain, Quality, and other stakeholders to gather facts and technical information.
  • Conduct and document root cause investigations using structured problem-solving methodologies.
  • Develop robust corrective and preventive action (CAPA) plans based on investigation outcomes.
  • Analyze manufacturing and quality data to support investigation conclusions.
  • Ensure investigations are completed accurately, thoroughly, and within required timelines.
  • Support continuous improvement initiatives related to quality systems and manufacturing processes.
  • Maintain compliance with GMP regulations, internal procedures, and quality standards.
  • Simplify complex technical events into clear, concise, and audit-ready documentation.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Chemistry, Biotechnology, or a related technical discipline.
  • Minimum 3 years of experience in technical writing within a regulated GMP environment.
  • Experience authoring deviation investigations in pharmaceutical, biopharmaceutical, or biotechnology manufacturing.

Strong knowledge of:

  • Root Cause Analysis
  • CAPA Development
  • Deviation Management
  • GMP Regulations
  • Experience using investigation tools such as:
  • Fishbone Analysis
  • 5 Whys
  • Failure Analysis Techniques
  • Familiarity with Electronic Quality Management Systems (eQMS).
  • Strong Microsoft Word and Excel skills.
  • Excellent communication, documentation, and cross-functional collaboration abilities.