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Msat Associate Director Jobs (NOW HIRING)

Sana Biotechnology

MSAT Engineer

Cambridge, MA

$120K - $150K/yr

As an MSAT Engineer, you will report to the Executive Director of MSAT and support manufacturing of Sana's stem cell-derived pancreatic islet cell program for persons with type 1 diabetes (SC451)

Sana Biotechnology

MSAT Engineer

Cambridge, MA · On-site

$120K - $150K/yr

As an MSAT Engineer, you will report to the Executive Director of MSAT and support manufacturing of Sana's stem cell-derived pancreatic islet cell program for persons with type 1 diabetes (SC451)

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Msat Associate Director information

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$30.5K

$102.7K

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How much do msat associate director jobs pay per year?

As of Jun 26, 2026, the average yearly pay for msat associate director in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an MSAT Associate Director, and why are they important?

To thrive as an MSAT (Manufacturing Science and Technology) Associate Director, you need deep expertise in bioprocess engineering, technology transfer, and process validation, typically supported by an advanced degree in a life science or engineering discipline. Familiarity with cGMP regulations, quality management systems, statistical analysis tools, and process simulation software is essential. Strong leadership, cross-functional collaboration, and problem-solving abilities distinguish top performers in this role. These skills ensure effective oversight of manufacturing processes, regulatory compliance, and the successful introduction of new technologies or products.

What is the difference between Msat Associate Director vs Msat Manager?

AspectMsat Associate DirectorMsat Manager
ResponsibilitiesOversees multiple projects, strategic planning, and team leadershipManages daily project operations, client communication, and team coordination
Required CredentialsTypically requires advanced degrees and relevant certificationsRequires relevant experience and certifications, but often less senior
Work EnvironmentStrategic, leadership-focused, often in corporate or consulting settingsOperational, client-facing, and team management roles
Industry UsageCommon in consulting, healthcare, and technology sectorsWidely used in similar industries for mid-level management roles

The Msat Associate Director role is more strategic and leadership-oriented, overseeing broader initiatives and teams, while the Msat Manager focuses on daily project execution and client interactions. Both roles require relevant credentials and experience, but the Associate Director typically holds a higher level of responsibility and strategic influence.

How does an MSAT Associate Director typically collaborate with cross-functional teams in a pharmaceutical company?

An MSAT Associate Director frequently works with cross-functional teams such as R&D, Quality Assurance, Regulatory Affairs, and Manufacturing to ensure that processes are robust, scalable, and compliant with regulatory standards. They often serve as a bridge between technical operations and production teams, leading technology transfer initiatives and troubleshooting complex manufacturing issues. Effective communication and project management skills are crucial, as the role involves coordinating timelines, aligning objectives, and facilitating knowledge transfer between different departments to support successful product launches and ongoing manufacturing processes.

What is an MSAT Associate Director?

An MSAT Associate Director is a senior professional responsible for leading the Manufacturing Science and Technology (MSAT) team within a pharmaceutical or biotechnology company. This role oversees the development, optimization, and troubleshooting of manufacturing processes to ensure product quality and regulatory compliance. The Associate Director collaborates with cross-functional teams, manages technology transfer, and supports the scale-up of production from research to commercial manufacturing. They play a key role in driving process improvements and ensuring that manufacturing operations run efficiently and effectively.
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Msat Associate Director jobs near you
Infographic showing various Msat Associate Director job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 88% In-person, and 12% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Associate Director of Biomanufacturing

Advanced Regenerative Manufacturing Institute Inc

Manchester, NH • On-site

Full-time

Posted 29 days ago

Job description

Overview

The Advanced Regenerative Manufacturing Institute (ARMl)IBioFabUSA is a Member-based non-profit, member-driven, public-private partnership with a mission to advance the bioeconomy and transform the future of human health. ARMI provides technical and wrap-around commercialization services to companies seeking to advance technologies that will contribute to this impact.

The Impact That You Will Make

ARMI is seeking an independent, self-starter with Manufacturing, Science and Technology (MSAT) experience to lead our phase-appropriate cell therapy manufacturing team. The successful candidate will be responsible for oversight of daily manufacturing operations ensuring the generation of high-quality, cell-based therapy products for use in both research and Phase 1 clinical trials. This individual will lead a team of scientists and technicians working to bring early phase manufacturing processes into phase-appropriate compliance with Good Manufacturing Practices (GMP). This role requires particularly strong attention to detail, a deep understanding of phase-appropriate GMP manufacturing, and the ability to think outside the box to solve problems creatively and proactively. The ideal candidate will have experience with tech transfer, aseptic technique and operations within a controlled manufacturing environment, SOP/Batch Record drafting, audit response support, deviations and CAPAs, continuous improvement activities, and other aspects of contract manufacturing.

Your Role

Leadership and Oversight

  • Lead daily manufacturing operations/tasks.
  • Ensure team compliance with GMP and safety standards.
  • Coach team members on root-cause analysis, documentation, and CAPA.
  • Collaborate with cross-functional teams including Quality, Facilities, and Project Management.
  • Manage multiple projects simultaneously and confidentially while meeting critical timelines and deliverables.
  • Work with the broader management team to develop work schedules ensuring robust coverage.
  • Support regulatory submissions and client/internal/regulatory audits as needed.
  • Manage external communications on project as needed.

Process Execution & Documentation

  • Conduct technology transfers into and within ARMI's facility.
  • Draft and review/approve accurate SOPs, technical documentation, batch records, and detailed reports as needed.
  • Monitor process performance through data analysis.
  • Investigate production deviations and manufacturing issues, performing root cause analysis, and implementing corrective actions.

Instrumentation & Maintenance

  • Collaborate with Operations, service engineers, and vendors for process equipment, calibration, preventative maintenance, optimization, and upgrades.
  • Ensure proper training of laboratory personnel on process and safety procedures.

Your Skills and Experiences

Education & Experience

  • Biotechnology, Biology, Biochemistry, or related life science degree. BS/MS with 10-15 years of experience or PhD with 4-6 years of experience in cell therapy manufacturing in an MSAT or GMP production role.
  • Familiarity with phase appropriate GMP and relevant FDA regulations and requirements.
  • Demonstrated experience leading teams and cross-functional interactions.

Technical Skills

  • Extensive proficiency with cell therapy manufacturing.
  • Experience with clean room operations for cell therapy production.
  • Familiarity with process equipment including a variety of cell culture technologies from flasks to stirred tank reactors, counterflow and continuous centrifugation, etc.
  • Demonstrated knowledge of GMP regulations, including change control, deviations, CAPA, etc.
  • Understanding process modeling, data analysis software (e.g., Minitab, JMP), and statistical methods (e.g. ANOVA).
  • Experience with Phase appropriate application of regulations
  • Familiarity with project management tools and techniques

Personal Attributes

  • Commitment to quality, scientific integrity, and company mission
  • Strong analytical and proactive problem-solving skills with a strong attention to detail
  • Excellent written and verbal communication abilities
  • Ability to work independently and manage competing priorities
  • Team-oriented mindset with collaborative cross-functional approach

Working Conditions

  • Cleanroom laboratory environment with exposure to biologics, chemical reagents, and analytical instruments
  • Weekend and holiday coverage may be required
  • Occasional overtime may be required to meet project deadlines
  • Some travel may be required for conferences, training, or client meetings

By applying, I understand that any offer of employment is contingent upon the successful completion of a background check, in accordance with applicable laws.

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