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Head Of Msat Jobs (NOW HIRING)

$125 - $150/hr

... Head of Product Quality and Regulatory. Prepares CMC regulatory strategies that enable first pass ... Serve as a point of contact with Development, MSAT, Manufacturing, Quality Assurance, Validation ...

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Head Of Msat information

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$22K

$96.6K

$221K

How much do head of msat jobs pay per year?

As of Sep 9, 2026, the average yearly pay for head of msat in the United States is $96,611.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $125,500.00 per year, depending on experience, location, and employer.

What are the roles and responsibilities of a Head of MSAT?

The Head of MSAT (Manufacturing Science and Technology) is responsible for leading teams that bridge the gap between process development and commercial manufacturing in industries such as pharmaceuticals or biotechnology. Their main duties include overseeing process optimization, technology transfer, troubleshooting, and ensuring that manufacturing processes remain efficient, compliant, and up to date with regulatory standards. They also collaborate closely with R&D, quality, and production teams to support product scale-up and resolve complex technical issues. Strong leadership, technical expertise, and communication skills are essential for this role.

What skills and qualifications are needed to thrive as a Head of MSAT?

A Head of MSAT requires deep expertise in process development, technology transfer, and bioprocess engineering, usually supported by an advanced degree in life sciences or engineering. Familiarity with GMP regulations, quality management systems, and process analytical technologies (PAT) is essential, often complemented by Six Sigma or Lean certifications. Strong leadership, problem-solving, and cross-functional communication skills help drive innovation and ensure effective collaboration between manufacturing, quality, and R&D teams. These competencies are vital for maintaining product quality, regulatory compliance, and continuous process improvement in biopharmaceutical manufacturing.

How does the Head of MSAT collaborate with cross-functional teams to drive process improvements in biomanufacturing?

The Head of MSAT (Manufacturing Science and Technology) plays a central role in coordinating with departments such as Quality Assurance, Engineering, Process Development, and Operations. They facilitate technical transfers, troubleshoot complex manufacturing issues, and ensure alignment on process optimization initiatives. Regular meetings, joint problem-solving sessions, and data sharing are common practices, allowing for effective communication and seamless implementation of process improvements. This collaborative approach not only enhances product quality and efficiency but also supports regulatory compliance and continuous innovation.

What is the difference between Head Of Msat vs Customer Success Manager?

AspectHead Of MsatCustomer Success Manager
Primary FocusOversees post-sales customer support and satisfaction strategiesManages customer relationships to ensure product adoption and retention
Required CredentialsTypically requires technical knowledge, leadership experience, and industry certificationsRequires strong communication skills, customer service experience, and industry knowledge
Work EnvironmentStrategic leadership in a technical or SaaS environmentCustomer-facing roles within sales or support teams

The Head Of Msat focuses on leading customer support teams and developing strategies to improve customer satisfaction, often with a technical or strategic emphasis. In contrast, a Customer Success Manager directly manages customer relationships to ensure product success and retention. Both roles are vital in customer-centric organizations but differ in scope and responsibilities.

What states have the most Head Of Msat jobs?

States with the most job openings for Head Of Msat jobs include:

What are popular job titles related to Head Of Msat jobs?

For Head Of Msat jobs, the most frequently searched job titles are:

Infographic showing various Head Of Msat job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $96,611 per year, or $46.4 per hour.

Head of Process Automation, Foster City Biologics Manufacturing

Foster City, CA • On-site

Gilead Sciences, Inc.
Scientific Research and Development Services • 10K+ employees

Full-time

Medical, Dental, Vision, Life, PTO

Posted 21 days ago


Gilead Sciences rating

8.9

Company rating: 8.9 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

9th of 86 rated pharmaceutical


Job description

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description
At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.
We set and achieve bold ambitions in our fight against the world's most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As the Head of Process Automation, Foster City Biologics Manufacturing, you will hold a key leadership role accountable for defining and executing the site process automation strategy, operating model, governance, and lifecycle roadmap for DeltaV-based process equipment automation supporting the Foster City Manufacturing New Chess Facility (NCF) and the biologics Pilot Plant within the New Technical Development Center (NTDC).
This role will lead a high-performing organization of internal engineers and specialized contract resources through design, startup, qualification, operational readiness, and steady-state lifecycle support while ensuring alignment with manufacturing, digital, quality, compliance, and enterprise automation priorities.
The position serves as the business owner and technical authority for DeltaV process automation systems supporting GMP and non-GMP biologics drug substance manufacturing, including bioreactors, chromatography systems, TFF, filtration, harvest, buffer/media preparation, and associated batch execution capabilities. The role will work closely with pilot and GMP Manufacturing, MSAT, Corporate Operations Automation, Engineering, Validation, Quality, IT, Tech Dev, and equipment vendors to create a robust, agile, scalable, and compliant automation ecosystem.
Job Responsibilities:
NCF and NTDC Automation Strategy & Delivery
  • Serve as the site DeltaV process automation owner for NCF and NTDC from detailed design through operational readiness and ongoing production.
  • Define and execute the automation roadmap for DeltaV process control systems.
  • Collaborate closely with IT and Corporate Operations Automation to establish the Foster City biologics pilot and manufacturing facilities as industry leading digital biologics facilities - integrating DeltaV, MES, Process Parameter management, BAS, ERP, LIMS, Historian and analytics platforms.
  • Establish site process automation standards, governance, and lifecycle management processes.
  • Ensure alignment with manufacturing objectives, digital manufacturing strategy, and future facility expansion plans.
  • Represent process automation on site governance, project steering, startup, and operational readiness teams.
  • Partner across Gilead and Kite to develop a vision, roadmap, and implementation strategy for compliant and responsible use of AI in manufacturing automation.

DeltaV System Ownership
  • Own the DeltaV platform supporting GMP and non-GMP process equipment in Foster City across the biologics manufacturing process.
  • Oversee system architecture, configuration standards, batch control strategy, alarm philosophy, historian integration, and recipe governance.
  • Ensure systems maintain validated status and comply with applicable GxP, data integrity, and cybersecurity requirements.
  • Lead lifecycle management activities including upgrades, patching, obsolescence planning, backup/recovery, and disaster recovery readiness.
  • Establish a standardized and reusable DeltaV code base to support long-term scalability and supportability.

Organization Building & Leadership
  • Build, lead, and scale a fit-for-purpose process automation organization consisting of internal employees, matrixed partners, and contract resources, with clear roles, decision rights, technical capability expectations, and accountability for delivery, operational support, and lifecycle ownership.
  • Develop a sustainable support model for startup and steady-state operations.
  • Define and implement a sustainable support model for startup and steady-state operations, including escalation coverage, vendor and contractor interfaces, knowledge management, service levels, and coordination with the Corporate Operations Automation organization.
  • Recruit, mentor, coach, develop, and retain automation engineers and technical specialists while building a leadership pipeline and promoting differentiated career growth for high-performing technical talent.
  • Foster a culture of technical excellence, ownership, reliability, safety, compliance, and continuous improvement.

Project Execution (NTDC and NCF)
  • Accountable for site process automation deliverables for design reviews, FATs, SATs, commissioning, qualification, and startup.
  • Work with an enterprise mindset to ensure project deliverables meet schedule, cost, quality, and compliance objectives.
  • Drive timely issue resolution during facility construction, startup, and GMP operations.
  • Support technology transfer and process implementation activities alongside MSAT, Tech Dev, and Manufacturing.

Operational Support
  • Establish procedures and governance for automation incident management, change control, deviation support, and CAPA execution.
  • Lead troubleshooting of complex automation and batch execution issues.
  • Partner with Operations to maximize system availability, reliability, and manufacturing throughput.
  • Develop site automation KPIs and reliability metrics.
  • Manage system integrators, automation contractors, OEMs, and engineering partners.
  • Serve as escalation point for critical automation-related production events.

Compliance & Cybersecurity
  • Ensure compliance with GxP, 21 CFR Part 11, Annex 11, data integrity requirements, and corporate quality standards as applicable.
  • Lead OT cybersecurity activities for process automation systems in partnership with IT and cybersecurity organizations.
  • Support inspections, audits, and regulatory interactions related to automation systems.

Requirements:
  • Bachelor's degree in Engineering, Automation, Chemical Engineering, Electrical Engineering, Computer Engineering, or related technical discipline with 10+ years of relevant experience (defined below) required OR
  • Masters degree in Engineering, Automation, Chemical Engineering, Electrical Engineering, Computer Engineering, or related technical discipline with 8+ years of relevant experience (defined below) OR
  • PhD in Engineering, Automation, Chemical Engineering, Electrical Engineering, Computer Engineering, or related technical discipline with 5+ years of relevant experience (defined below)
  • Relevant experience: direct, matrixed, or cross-functional leadership experience, including experience building teams, leading technical managers or senior individual contributors, managing external partners, and influencing senior stakeholders in a regulated manufacturing environment.
  • Relevant experience: automation, process control, or manufacturing systems experience in biopharmaceutical, biotechnology, or regulated manufacturing environments, including extensive experience with DeltaV-based GMP manufacturing automation and lifecycle ownership.

Preferred Qualifications:
  • Advanced degree preferred

Technical Expertise
  • Deep knowledge of Emerson DeltaV, with the ability to set technical direction, challenge design decisions, assess risk, and guide expert engineers and integrators.
  • Expert knowledge of batch automation and ISA-88 principles.
  • Experience supporting biologics Drug Substance manufacturing processes.
  • Experience with GMP validation and computerized systems compliance.
  • Knowledge of historian systems, automation networking, industrial cybersecurity, and OT infrastructure.
  • Experience with large capital projects, facility startup, and operational readiness activities.
  • Up-to-date knowledge of industry developments and best practices in automation, OT, digital manufacturing, and manufacturing systems integration.

Demonstrated Leadership Capabilities
  • Building teams and organizational capabilities from the ground up.
  • Strong collaboration, stakeholder management, and influencing skills.
  • Ability to balance strategic planning with hands-on technical problem solving.
  • Ability to lead through ambiguity and startup environments.

People Leader Accountabilities:
  • Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
  • Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
  • Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.

The salary range for this position is: $195,670.00 - $253,220.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
https://www.gilead.com/careers/compensation-benefits-and-wellbeing
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
For jobs in the United States:
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.

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