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Director Process Chemistry Jobs in Oregon (NOW HIRING)

Kanto Corporation

Director of Quality

Portland, OR · On-site

$160K - $190K/yr

Lead Quality. Shape Processes. Drive Change. About Kanto Corporation Kanto is a leading U.S ... Bachelor's degree in Chemical Engineering/Sciences, Chemistry, Life Sciences (Master's preferred ...

Spyre Therapeutics

Associate Director, Medical Writing

OR · On-site +1

$170K - $199K/yr

Proactively contribute to process improvements and standards across the team. Develop or maintain ... Bachelor's degree in a scientific discipline, preferably in Pharmacy, Chemistry, Biology, or ...

QuantumClean

R&D Engineer III

Hillsboro, OR

Design and direct process characterization studies * Develop process control strategies for new and ... Uses knowledge in engineering, chemistry, and physics to develop new products, coatings, cleaning ...

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Showing results 21-40

All JobsProcess Chemistry JobsDirector Process Chemistry JobsDirector Process Chemistry Jobs in Oregon

Director Process Chemistry information

See Oregon salary details

$43.3K

$89.6K

$138.5K

How much do director process chemistry jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director process chemistry in Oregon is $89,639.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,400.00 and $111,000.00 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.

What are popular job titles related to Director Process Chemistry jobs in Oregon?

For Director Process Chemistry jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Director Process Chemistry jobs in Oregon look for?

The top searched job categories for Director Process Chemistry jobs in Oregon are:

What cities in Oregon are hiring for Director Process Chemistry jobs?

Cities in Oregon with the most Director Process Chemistry job openings:

Director Process Chemistry jobs near you
Infographic showing various Director Process Chemistry job openings in Oregon as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $89,639 per year, or $43.1 per hour.

Director, Product Development Quality

Telix Pharmaceuticals (AMER)

OR • On-site, Remote

Full-time

Posted 25 days ago

Job description

See Yourself at Telix

As the Director, Product Development Quality, you will lead the Development Quality function, supporting radiopharmaceutical development programs from early clinical development through registration-readiness. This role carries direct accountability for leading and scaling a high-performing Development Quality team to support the organization's strategic transition from PET diagnostics into radiopharmaceutical therapeutics. You will establish and govern QMS elements specific to development-stage programs, represent Quality at the leadership level, and serve as a primary Quality interface with regulatory agencies, CDMOs, and clinical supply partners. The ideal candidate is a seasoned quality leader with deep expertise in radiopharmaceutical GMP, development-stage quality experience, and the ability to lead cross-functional quality execution in a high-growth environment.

Key Accountabilities:

  • Good Manufacturing Practices (GMP)
    • Provide GMP quality oversight for development-stage radiopharmaceutical programs, including alignment with applicable ICH, FDA, EMA, PMDA, USP <821>, and relevant 10 CFR requirements governing radioactive drug substances and drug products.
    • Partner with cross-functional teams to apply fit-for-purpose GxP expectations for radiopharmaceutical development programs.
    • Support quality oversight for short half-life manufacturing considerations specific to radiopharmaceuticals, including real-time release testing (RTRT), compressed batch release timelines, and in-process control strategies.
    • Coordinate with technical teams and the Radiation Safety Officer, as appropriate, on quality interfaces related to hot-cell qualification, dose calibrator validation, and radiation safety program requirements.
  • Development Quality and Clinical Supply Oversight
    • Provide Development Quality input and oversight for IND/CTA submissions, clinical-stage GMP activities, and CTD Module 3 quality content.
    • Support quality activities related to clinical investigational medicinal product supply, including CDMO oversight, comparator sourcing, clinical packaging, labeling, distribution, and release requirements.
    • Review and provide quality input on development program documentation, including manufacturing records, specifications, validation documentation, deviations, CAPAs, and change controls.
  • Quality Systems and Process Improvement
    • Support the implementation and continuous improvement of Development Quality procedures, templates, and governance practices.
    • Ensure development-stage quality processes are appropriately documented, scalable, and aligned with enterprise Quality standards.
  • Partner with Quality leadership to identify gaps, assess risks, and recommend pragmatic solutions for development-stage programs, Cross-Functional Leadership and External Partner Oversight
    • Represent Development Quality in program team meetings, stage-gate discussions, and cross-functional governance forums.
    • Partner with Regulatory Affairs, CMC, Clinical Operations, Manufacturing, Supply Chain, and external partners to ensure quality risks are identified, escalated, and managed.
    • Provide quality oversight of contracted manufacturing, testing, packaging, and clinical supply partners supporting development programs.
  • Regulatory Compliance & Inspection Readiness
    • Support regulatory agency interactions, inspections, and submission-related activities as the Development Quality representative.
    • Provide input on development quality risk assessments when regulatory or GMP requirements cannot be fully integrated.
  • Support inspection readiness activities for development-stage programs and external partners. People Leadership
    • Lead and develop Development Quality team members, including coaching, workload management, performance feedback, and capability building.
    • Support headcount planning and organizational capability development as the Development Quality function matures.
    • Promote consistent quality decision-making, documentation practices, and cross-functional collaboration.

Education and Experience:

  • Advanced degree (MS, PharmD, PhD) in a relevant scientific discipline (Pharmacy, Chemistry, Radiochemistry, or related field) strongly preferred; bachelor's degree with equivalent experience considered.
  • 10+ years of progressive quality experience within the pharmaceutical, biotechnology, or radiopharmaceutical industry, with demonstrated depth in development-stage GMP quality.
  • 7+ years of leading and developing quality teams, including experience building greenfield or newly established quality functions.
  • Direct experience in radiopharmaceutical quality required, including familiarity with short half-life manufacturing, real-time release testing, and USP <821> compliance; oncology or targeted therapy development quality experience preferred.
  • Demonstrated experience with IND/CTA submissions, NDA/BLA quality strategy, and CTD Module 3 authorship or oversight; direct regulatory agency interaction experience (FDA, EMA, and/or PMDA) required.
  • Comprehensive understanding of Good Manufacturing Practices (GMP) and regulatory requirements.
  • Proven ability to work with cross-functional teams and maintain effective relationships with key business partners.
  • Strong communication and educational skills to support GxP and regulatory knowledge across the organization.
  • Experience in documentation practices and record-keeping, ensuring accuracy and compliance.

Key Capabilities:

  • Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
  • Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
  • Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
  • Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
  • Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
  • Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
  • Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
  • Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
  • Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
  • Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

Apply