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Director Process Development Jobs in Poway, CA (NOW HIRING)

Superlanet

Business Development Director

San Diego, CA · On-site

$130K - $180K/yr

Role Overview Superlanet is seeking a Business Development Director to build and grow our business ... This individual will establish structure and processes, develop and oversee a high-performing sales ...

Actalent

Senior Process Engineer

Carlsbad, CA

$106K - $138K/yr

You will lead process development for flip chip assembly and thermo-compression bonding, support 2 ... values direct impact and ownership. The typical schedule runs from 8:00 AM to 5:00/5:30 PM, with ...

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All JobsProcess Development JobsDirector Process Development JobsDirector Process Development Jobs in Poway, CA

Director Process Development information

See Poway, CA salary details

$44K

$84.5K

$165.7K

How much do director process development jobs pay per year?

As of Aug 19, 2026, the average yearly pay for director process development in Poway, CA is $84,495.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,300.00 and $99,700.00 per year, depending on experience, location, and employer.

What does a director of process development do?

A Director of Process Development is responsible for overseeing the design, implementation, and optimization of processes within an organization, typically in manufacturing, biotech, or pharmaceutical industries. They lead teams to develop efficient, cost-effective, and scalable processes for producing products or delivering services. This role often involves coordinating cross-functional teams, ensuring regulatory compliance, and driving continuous improvement initiatives. The Director also collaborates with R&D, quality, and production departments to bring new products from concept to commercial scale.

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

To thrive as a Director of Process Development, you need deep expertise in process engineering, project management, and a strong background in chemistry, biochemistry, or a related field, often supported by an advanced degree. Familiarity with process modeling software, statistical analysis tools, and industry-specific quality standards such as GMP or Six Sigma certifications is typically required. Exceptional leadership, strategic thinking, and cross-functional communication skills set top performers apart in this role. These abilities are essential for driving efficient process innovation, ensuring regulatory compliance, and leading teams toward operational excellence.

How does a director of process development typically collaborate with cross-functional teams to drive project success?

As a Director of Process Development, you will regularly work alongside R&D, Quality Assurance, Manufacturing, and Regulatory Affairs teams to ensure new processes are scalable, compliant, and align with business goals. This collaboration often involves leading cross-departmental meetings, aligning on project milestones, and troubleshooting process bottlenecks together. Strong communication and leadership skills are crucial, as you’ll be responsible for integrating feedback, managing diverse perspectives, and ensuring that project deliverables are met on time and within budget.

What is the difference between Director Process Development vs Process Engineer?

AspectDirector Process DevelopmentProcess Engineer
CredentialsBachelor's/Master's in Engineering or related field, often with leadership experienceBachelor's or Master's in Engineering or related field
Work EnvironmentStrategic planning, team leadership, cross-department collaborationHands-on process design, optimization, and troubleshooting
Industry UsageCommonly used in biotech, pharma, and manufacturing industriesUsed across similar industries for process development and improvement

The main difference is that the Director Process Development oversees strategic process initiatives and manages teams, while the Process Engineer focuses on executing process improvements and technical tasks. The director role involves higher-level planning and leadership, whereas the engineer role is more hands-on and technical.

What job categories do people searching Director Process Development jobs in Poway, CA look for?

The top searched job categories for Director Process Development jobs in Poway, CA are:

What cities near Poway, CA are hiring for Director Process Development jobs?

Cities near Poway, CA with the most Director Process Development job openings:

Director Process Development jobs near you

Associate Director - Senior Director, CMC Formulation Development

Kumquat Biosciences Inc

San Diego, CA • On-site

$170K - $275K/yr

Full-time

Re-posted 3 hours ago

Job description

Kumquat Biosciences is committed to the discovery and development of innovative drugs to transform cancer treatments. Kumquat brings together an accomplished management team and distinguished scientific founder to translate innovative research to novel therapeutics. Our team has a proven track record of drug discovery and development, having played pivotal roles in the discovery of multiple clinical-stage compounds as well as an approved drug for the treatment of cancers and immune-mediated inflammatory diseases.
We are currently seeking a highly motivated, creative CMC formulation professional at associate director or director level to join our CMC team in San Diego. This candidate will report to the Executive Director and Head of CMC. This candidate is expected to work closely with Kumquat internal discovery and development teams as well as external CRO/CDMO companies to drive programs into early and late clinical development. This is a position with responsibility for formulation strategy design, process development and manufacturing. The ideal candidate will have an in-depth understanding in all aspects of oral solid dosage formulations and injectable formulations. A strong team player who is detail-oriented and has the desire to learn and understand life-cycle product management concepts and practice is essential. The candidate will have the opportunity to work on multiple programs within the company's pipeline which comprises potentially first-in-class approaches & novel-novel targets.
Role responsibilities
  • Understand the development candidate's physicochemical properties and target product profile to evaluate formulation options and design phase appropriate formulations at different development stages.
  • Select external CRO/CDMO partners based on project needs and the external parties' technical capabilities, quality system, and track records.
  • Prepare RFPs and evaluate proposals based on the targeted product quality, project timeline, and budget.
  • Plan and oversee drug product process optimization, GMP manufacturing, packaging, labeling, stability testing activities.
  • Track process development/validation history and manage CMC drug product related documents in support of life cycle of quality improvement and regulatory filing/updates.
  • Work closely with a cross-functional team within and outside of the CMC department to align with key stakeholders (CMC, Clinical, Quality Assurance and Regulatory).
  • Author and review CMC drug product related sections for regulatory filing and annual updates.
  • Stay current on industry trends and regulatory requirements to ensure delivery of quality products under cGMP environment.
  • Prepare and communicate research results in both oral and written format.
  • Supervise junior CMC Drug product team members.
  • Contribute to a fast-paced, dynamic, data-driven scientific culture that embraces innovation and excellence.

Requirements
  • Ph.D. or M.S. in chemistry, chemical engineering, pharmaceutical science, or related discipline with at least 10 years of industry experience (title for this position will be commensurate with the candidate's experience and qualifications)
  • Highly familiar with current formulation principles and industry practices.
  • Extensive process development/ optimization, scale-up and process validation expertise, with emphasis on solid oral dosage forms.
  • Experience with injectable formulations and modern enabling technologies is a plus.
  • Track record of accomplishment in managing CMC drug product projects at early and late development stages.
  • Ability to enable external CRO/CDMO to achieve project goals on time and under budget.
  • Strong written and communication skills, good problem-solving abilities, and an ability to work effectively with a diverse team of co-workers in a dynamic environment.
  • Bilingual proficiency in English and Chinese (verbal and written) preferred but not required.

Kumquat Biosciences offers an attractive salary and benefits package, including equity incentives.
Salary Description: $170k - $275k
Salary Description
$170k - $275k

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