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Director Process Chemistry Jobs (NOW HIRING)

Gilead

Intern - PDM - Process Chemistry

Foster City, CA · On-site

$20/hr

... direct impact. We believe every employee deserves a great leader. People Leaders are the ... Intern - PDM-Process Chemistry As a Gilead intern you will contribute to high-impact meaningful ...

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Amrize

Process Safety Management Director

Houston, TX · On-site

ABOUT THE ROLE The Director, Process Safety Management (PSM) will provide strategic leadership ... Deep, demonstrable expertise in OSHA 1910.119, EPA RMP regulations, process chemistry, industrial ...

Micron

Director, Process Hazard Analysis

Boise, ID · On-site

Micron is seeking a Director to lead the Process Hazard Analysis (PHA) organization within the ... Master's degree in Engineering, Chemistry, or a related technical field * 10+ years of experience ...

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How much do director process chemistry jobs pay per year?

As of Sep 11, 2026, the average yearly pay for director process chemistry in the United States is $84,782.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $105,000.00 per year, depending on experience, location, and employer.

What does a director of process chemistry do?

A Director of Process Chemistry leads teams responsible for developing and optimizing chemical processes used in the production of pharmaceuticals or other chemicals. They oversee process development from laboratory scale to full manufacturing, ensuring efficiency, safety, and regulatory compliance. This role involves collaboration with R&D, manufacturing, and quality teams to deliver scalable and cost-effective chemical synthesis solutions. Directors also manage budgets, mentor staff, and may interact with regulatory agencies to support product approval.

What are the key skills and qualifications needed to thrive as a director of process chemistry?

A Director of Process Chemistry typically requires a Ph.D. in chemistry or chemical engineering, extensive experience in process development and scale-up, and a strong foundation in organic synthesis. Familiarity with analytical instrumentation, process safety systems, and regulatory compliance, as well as proficiency in software for data analysis and project management, are commonly expected. Exceptional leadership, communication, and problem-solving skills help foster innovation and guide multidisciplinary teams effectively. These competencies are vital for ensuring efficient, safe, and cost-effective chemical manufacturing processes that meet organizational goals and industry standards.

How does a director of process chemistry typically collaborate with cross-functional teams during drug development?

A Director of Process Chemistry works closely with teams such as Analytical Development, Formulation, Quality Assurance, and Regulatory Affairs to ensure smooth progression of drug candidates from lab to manufacturing scale. Collaboration involves regular meetings to align on project timelines, address technical challenges, and implement process improvements. This role often leads technology transfer discussions and troubleshooting sessions, ensuring process scalability and compliance with regulatory requirements. Effective communication and interdisciplinary teamwork are essential for success in this leadership position.

What is the difference between Director Process Chemistry vs Process Development Manager?

AspectDirector Process ChemistryProcess Development Manager
CredentialsAdvanced degree in Chemistry or Chemical Engineering, extensive industry experienceSimilar educational background, often with several years of industry experience
Work EnvironmentStrategic leadership, overseeing multiple projects and teamsHands-on process development, project management, and team coordination
Industry UsageUsed in pharmaceutical, chemical, and biotech industries for high-level oversightCommonly found in R&D and manufacturing settings for process optimization

The main difference is that the Director Process Chemistry focuses on strategic leadership and overall process chemistry direction, while the Process Development Manager handles day-to-day process development and project execution. Both roles require similar credentials but differ in scope and responsibilities.

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Director Process Chemistry jobs near you
Infographic showing various Director Process Chemistry job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $84,782 per year, or $40.8 per hour.

Associate Scientific Fellow, Process Chemistry

Cambridge, MA • On-site

Takeda Pharmaceutical Company Limited
Investment Clubs and Venture Capital Companies • 1 - 10 employees
Learn more about Takeda Pharmaceutical Company Limitedexternal

Full-time

Re-posted 21 days ago

Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Scientific Fellow, Process Chemistry in our Cambridge office.

At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Here, you will be a vital contributor to our inspiring, bold mission.

OBJECTIVE:

The Associate Scientific Fellow in Process Chemistry is a recognized technical leader with deepexpertisein process chemistry development for synthetic molecules. Theymaintaina strong interest in laboratory work and play a critical role in advancing the portfolio by developing and executing complex scientific strategies across multiple late-stage pipeline projects,leveragingboth personal laboratory contributions and leadership of internal and external efforts.

The Associate Scientific Fellow drives the design and development of robust, scalablesynthetic routes, balancing safety, sustainability, cost, and quality. They foster strong cross-functional partnerships across SMPD, Pharm Sci, and commercial organizations to enable efficient technology transfer and lifecycle process development.

They may develop and lead project-focused academic collaborations to generate novel solutions to complex technical challenges. This includes initiating andparticipatingin projects involving significant scientific challenges with well-considered risk and high potential impact, as well as directing and managing external partnerships and outsourcing across a product platform, asappropriate.

The Associate Scientific Fellow is also expected to positivelyimpactthe scientific development of colleagues through training and mentoring and to promote the department externally by leading or contributing to multidisciplinary technical teams, driving peer-reviewed publications, andparticipatingin external conferences and scientific forums

ACCOUNTABILITIES:

  • Recognized as a technical expert within Process Chemistry, SMPD, and across Pharm Sci, providing scientific leadership in synthetic molecule process development.

  • Providesin-labmentorship and technical guidance to colleagues, elevating scientific rigor and problem-solving capabilities by modeling best practices, reviewing technical approaches, and strengthening overall organizational capability

  • Leads and executes complex scientific strategies across multiple late-stage programs, contributing directly through personal laboratory work and by guiding internal and external teams.

  • Designs and advances robust, scalable drug substance manufacturing processes, ensuring alignment with safety, sustainability, cost, and qualityobjectives.

  • Owns technical responsibility for one or more programs or key initiatives,ensuring integration of process understanding into development and manufacturing readiness.

  • Applies deep technicalexpertisetoidentify, assess, and mitigate scientific and process risks, enabling informed decision-making under conditions of uncertainty.

  • Develops and implements innovative solutions to complex synthetic and process challenges, incorporating emerging technologies and industry best practices.

  • Ensure strongcross-departmentcollaboration across SMPD (Process Research, Process Analytics, Process Engineering, Process Sciences&Technology,DS Portfolio Leadership), Pharm Sci,andcommercialmanufacturing partners to ensure effective technology transfer and lifecycle process development.

  • Leads and manages external partnerships, including CDMOs, academic collaborators, and consultants, to deliver high-quality outcomes aligned with program strategy.

  • Analyzes experimental data and process trends to build mechanistic understanding, extract key insights, and define forward-looking process strategies.

  • Contributes to and influences departmental and functional scientificstrategy, including identification and development of new capabilities and technology platforms.

  • Initiates and leads cross-functional or discipline-focused initiatives to address technical gaps and enable broader organizational impact.

  • Representsthe function internally and externally through technical leadership in multidisciplinary teams, publications, patents, and participation in scientific conferences.

  • Maintains and expands personal scientificexpertiseand externalnetworkto ensure continued innovation and thought leadership within Process Chemistry.

EDUCATION, EXPERIENCE AND SKILLS:

  • Bachelorsdegree and 15+ years relevant industry experience

  • Mastersdegree; 13+ years relevant industry experience

  • PhD; 7+ years relevant industry experience

  • Extensive experience in CMC pharmaceutical development for active pharmaceutical ingredients and drug products under cGMP's

  • Demonstrated deep technicalexpertisein synthetic molecule process chemistry and late-stage process development.

  • Proven record of significant technical contributions and scientific leadership within pharmaceutical development.

  • Experience working in multidisciplinary, cross-functional environments, with accountability for influencingprogram, departmental, or functional strategy.

  • Strong understanding of current Good Manufacturing Practices (cGMP) and their application to process development and manufacturing

Knowledge and Skills:

  • Analytical and Problem-Solving Skills - Applies advanced scientific reasoning to diagnose complex technical issues, assess risk, and develop effective, data-driven solutions under conditions of uncertainty.

  • Technical Expertise - Recognized specialist in one or more areas of process chemistry, with ability to apply deep mechanistic understanding to solve complex synthetic and process challenges.

  • Cross-Functional Collaboration - Effectively partners across global, multidisciplinary teams to integrate diverse perspectives and drive successful program outcomes.

  • Communication Skills - Communicates complex scientific concepts clearly and concisely to a range of audiences, including senior leadership; produces high-quality technical documentation suitable for internal and external use.

  • Leadership and Influence - Provides technical leadership and uses strong interpersonal skills to influence scientific direction, guide teams, and align stakeholders toward sharedobjectives.

  • Knowledge Sharing and Capability Building - Actively captures anddisseminatesknowledge, contributing to improved processes, scientific standards, and organizational learning.

  • External Engagement - Demonstrates active involvement in the scientific community through presentations, publications, and engagement with external partners;maintainsawareness of emerging trends and technologies.

  • Organization and Execution - Effectively prioritizes and manages multiple scientific and programobjectives, ensuring alignment with project timelines and organizational goals.

TRAVEL REQUIREMENTS:

May requireapproximately5-10% travel.

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law

This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

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Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

Cambridge, MA

U.S. Base Salary Range:

$154,400.00 - $242,550.00


The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.


For information about our benefits, please click here.


EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

LocationsCambridge, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Job Exempt

YesIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

San Diego, CA, US

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