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Msat Associate Director Jobs (NOW HIRING)

Servier

Assoc Director, Oral Solid Drug Product

Boston, KY · On-site

$198K - $207K/yr

Role Summary Within MSAT, the Oral Solid Drug Product team is responsible for providing technical ... The Associate Director, Oral Solid Drug Product serves as the technical subject matter expert for ...

GSK

Associate Director, Device Lead

Waltham, MA · On-site

Position Summary The Device Lead of Global MSAT Drug Delivery and Aseptic Technology will be the ... Support Device Director, Device Strategy and Device Procurement organizations on Continuous ...

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Msat Associate Director information

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$30.5K

$102.7K

$173K

How much do msat associate director jobs pay per year?

As of Sep 9, 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 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.

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 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.

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Msat Associate Director jobs near you
Infographic showing various Msat Associate Director job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Associate Director, CMC - Analytical Development

Boston, MA • On-site

AdvanCell
See more jobs at AdvanCellexternal

$170K - $220K/yr

Full-time

Posted 5 days ago

Job description

Partnering closely with Process Development, MSAT, Quality, Regulatory Affairs, and External Manufacturing partners, the Associate Director, CMC - Analytical Development provides strategic and technical leadership for analytical activities supporting the development and commercialization of ²¹²Pb-based APIs and radiopharmaceutical products.
The role is responsible for establishing phase-appropriate analytical strategies, specifications, and control approaches that support GMP manufacturing, product release, stability programs, and regulatory submissions.
The successful candidate leads CMC regulatory authoring and documentation related to analytical development and validation, reference standards, and stability programs, supporting global regulatory submissions, lifecycle management activities, and responses to health authority inquiries. The role also drives continuous improvement initiatives to strengthen analytical capability, product and process understanding, and the advancement of the company's radiopharmaceutical portfolio.
Working in close collaboration with Technical Development, MSAT, Quality, Engineering, and Operations, this position provides leadership across analytical method development, qualification, validation, transfer, and laboratory readiness activities to ensure robust and reliable analytical support for clinical and commercial manufacturing.
In addition, the Associate Director provides analytical expertise to the Sr. Director of Precursor Development and Director of External Manufacturing to support CDMO activities, manufacturing investigations, and the implementation of effective analytical control strategies. The role helps ensure alignment between internal development programs and external manufacturing operations to maintain a reliable, scalable, and compliant supply network.
Key Responsibilities and Duties
  • Develop phase-appropriate analytical CMC strategies and ensure generation of the supporting analytical data, technical documentation, and regulatory submission packages
  • Lead the development of phase-appropriate analytical control strategies, including analytical methods and release and stability specifications for drug substances and drug products, to support product development and regulatory objectives.
  • Partner with Technical Development, MSAT and CDMOs to support method development, qualification, validation, transfer, and troubleshooting activities, ensuring analytical methods are suitable for GMP manufacturing, release, and stability testing.
  • Ensure analytical development activities comply with GMP requirements and applicable radiopharmaceutical regulatory standards.
  • Provide technical leadership for regulatory interactions related to analytical methods, specification, control strategies, and comparability assessments.
  • Partner with Quality Assurance on investigations, change controls, and audit readiness activities
  • Provide targeted analytical support to Precursor Development and External Manufacturing for CDMO related activities.
  • Lead analytical investigation, troubleshoot manufacturing and development challenges, and drive continuous improvement initiatives
  • Mentor, coach, and develop Analytical Development staff.

Other Responsibilities
  • Observe the Company's workplace, health and safety, and regulatory policies and procedures.
  • Engage and communicate with other AdvanCell business unit staff to ensure that activities are undertaking seamlessly and effectively.
  • Adhere to the Company's quality management system processes and policies.
  • Other tasks as requested by the VP, CMC and Supply Chain

Essential Skills, Qualifications, Industry and Educational Requirements
  • M.Sc. in analytical chemistry, pharmaceutical sciences or a related discipline.
  • Minimum 3 years of experience in radiopharmaceutical industry with a focus on analytical and CMC development
  • Advanced understanding of (radio)pharmaceutical analytical method & validation, as well as quality control testing
  • Strong understanding of GMP requirements, (radio)pharmaceutical regulations, and industry standards across product development and commercialization
  • Excellent communication, technical writing and analytical problem-solving skills.
  • Demonstrated ability to build, mentor, and lead high-performing CMC teams
  • Proven ability to manage multiple priorities, meet timelines, and perform effectively in a fast-paced environment
  • Commitment to fostering a collaborative, inclusive, and diverse workplace culture.

Desirable Skills, Qualifications, Industry and Educational Requirements
  • Experience in alpha spectrometry
  • Experience in GMP manufacture of radiopharmaceuticals.
  • Sound understanding of regulatory requirements and guidelines governing GMP manufacture of radiopharmaceuticals and quality control (e.g. cGMP, PIC/S, ICH).

$170,000 - $220,000 a year

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