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Process Development Manager Jobs in Long Beach, CA

Development Manager

Orange, CA · On-site

$59K - $154K/yr

Development Manager Location: LA/OC Area (Remote) Reports to: Director, Development Wage Category ... Identify opportunities to improve processes, reporting, and operational efficiency to support ...

Showing results 21-40

Process Development Manager information

See Long Beach, CA salary details

$78.9K

$101.4K

$180.3K

How much do process development manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for process development manager in Long Beach, CA is $101,404.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,100.00 and $101,500.00 per year, depending on experience, location, and employer.

What does a process development manager do?

A process development manager oversees the design, implementation, and optimization of manufacturing or operational processes to improve efficiency, quality, and cost-effectiveness. They analyze workflows, collaborate with cross-functional teams, and often utilize tools like Six Sigma or Lean methodologies to develop scalable processes. Strong project management and problem-solving skills are essential in this role.

What are some common challenges faced by a process development manager, and how can they be addressed?

Process Development Managers often encounter challenges such as aligning cross-functional teams, managing resource constraints, and adapting processes to evolving business needs. Effective communication and collaboration with stakeholders in production, quality, and R&D are essential to overcome these obstacles. Proactively identifying potential bottlenecks, staying updated with industry best practices, and fostering a culture of continuous improvement can help ensure smoother process development and implementation.

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

AspectProcess Development ManagerProcess Engineer
ResponsibilitiesOversees process improvement projects, manages teams, develops strategies for scalable processesDesigns, tests, and implements specific manufacturing processes, focuses on technical execution
Required CredentialsBachelor's or Master's in Engineering, experience in process management, certifications like Six SigmaBachelor's in Engineering or related field, technical skills, certifications like Lean or Six Sigma
Work EnvironmentLeadership roles in manufacturing or R&D settings, cross-functional collaborationHands-on technical work in manufacturing or laboratory settings
Industry UsageCommon in manufacturing, pharmaceuticals, biotech industriesWidely used in manufacturing, chemical, and industrial sectors

The Process Development Manager focuses on strategic oversight and team leadership for process improvements, while the Process Engineer handles technical process design and implementation. Both roles require similar credentials and are integral to manufacturing industries, but differ in scope and responsibilities.

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

To thrive as a Process Development Manager, you need a solid background in process engineering, project management, and analytical problem-solving, typically supported by a degree in engineering, chemistry, or a related field. Familiarity with process simulation software, Lean Six Sigma methodologies, and quality management systems like ISO standards is commonly required. Strong leadership, communication, and change management skills help drive cross-functional collaboration and successful project implementation. These competencies are crucial for optimizing processes, ensuring product quality, and achieving operational efficiency in a competitive business environment.

What job categories do people searching Process Development Manager jobs in Long Beach, CA look for?

The top searched job categories for Process Development Manager jobs in Long Beach, CA are:

What cities near Long Beach, CA are hiring for Process Development Manager jobs?

Cities near Long Beach, CA with the most Process Development Manager job openings:

Associate Director, Process Development, Cell Therapy

AstraZeneca

Santa Monica, CA • On-site

$138K - $207K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

Position Summary
The Associate Director, Late-Stage Cell Therapy Process Development, will provide scientific and technical leadership for the development, characterization, and transfer of manufacturing processes for cell therapy products. This role is responsible for leading a team of scientists and engineers supporting process development activities from clinical development through commercialization, including BLA and global regulatory submissions. The successful candidate will partner cross-functionally with Manufacturing, Quality, Regulatory Affairs, Analytical Development, and CMC teams to ensure robust, compliant, and scalable manufacturing processes.
Key Responsibilities
Technical Leadership
  • Lead the late-stage process development for cell therapies within the Process Engineering function, managing multiple development projects

  • Direct and guide engineers/scientists to deliver high-quality technical documentation for the study design, laboratory execution and report authoring activities

  • Perform risk assessment, data analysis, write technical reports, and present outcome of the studies to cross-functional teams and governance forums

  • Conduct batch record review, deviation assessment, and data trending to ensure robustness of cell therapy manufacturing processes

  • Apply AI-enabled tools and digital analytics to accelerate data review, trend analysis, batch record evaluation, and process understanding

Team Leadership and Management
  • Build, develop, and manage a high-performing team of process development scientists and engineers

  • Establish project priorities, resource allocation, and departmental objectives

  • Foster a collaborative and innovation-driven culture

PPQ & Technology Transfer
  • Support PPQ activities including but not limited to protocol authoring, batch record authoring and planning

  • Support technology transfer of cell therapy processes to internal manufacturing sites including make-a-batch assessments and drafting manufacturing batch records

Lifecycle Management
  • Lead lifecycle management activities for commercial cell therapy products, including process monitoring, continuous improvement, post-approval changes, comparability assessments, and regulatory commitments.

  • Partner with Manufacturing, Quality, Regulatory Affairs, and Technical Operations to implement process improvements, maintain process control, and support ongoing commercial readiness.

Manufacturing Support & Scientific Deviation Management
  • Serve as the Process Development and Engineering SME for manufacturing operations, providing scientific support for deviations, investigations, atypical events, and process-related issues.

  • Lead root cause analyses, impact assessments, and CAPA development using data-driven and risk-based approaches to ensure product quality, compliance, and uninterrupted manufacturing operations.

Regulatory Support
  • Contributes to authoring and reviewing CMC documentation, including cell therapy process descriptions, characterization summaries, PPQ protocols and reports, and control strategy elements.

  • Support preparation of BLA/MAA submissions and responses to regulatory questions related to cell therapy manufacturing.

Cross-Functional Collaboration
  • Work closely with analytical sciences, quality, regulatory, and manufacturing teams to ensure end-to-end process alignment.

  • Represent cell therapy characterization activities in technical meetings, reviews, and governance discussions.

Required Qualifications
  • Ph.D. in Chemical Engineering, Biochemical Engineering, Biological Sciences, Biotechnology, Pharmaceutical Sciences, or related discipline with 6+ years of industry experience; or M.S. with 10+ years of relevant experience; or B.S. with 12+ years of relevant experience.

  • Strong technical expertise in cell therapy process development, GMP operations and late-stage / commercial readiness.

  • Experience with late-stage development, and PPQ for cell therapy processes.

  • Demonstrated proficiency in applying AI tools and digital solutions to data analysis, documentation, and workflow automation.

  • Strong technical writing, data analysis, and problem-solving skills.

Preferred Qualifications
  • Experience with commercial-stage cell therapy or biologics products.

  • Experience supporting PPQ, process validation, and post-approval changes.

  • Familiarity with global regulatory requirements and lifecycle management strategies.

  • Experience designing and executing DOE and multivariate data analysis for cell therapy processes.

Key Competencies
  • Strong team management and talent development experience

  • Excellent cross-functional communication and collaboration.

  • Ability to operate effectively in fast-paced, late-stage development environments.

  • Scientific curiosity, ownership mindset, and willingness to support manufacturing operations.

The annual base pay for this position ranges from $138K to $207K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
# Hybrid # Cell Therapy
Date Posted
10-Aug-2026
Closing Date
30-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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