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Pharmaceutical Project Engineer Jobs in California

Siegfried

Project Engineer III

Irvine, CA · On-site

As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards ... The Project Engineer III is responsible for leading and executing capital investment (CAPEX ...

Crane Company

Project Engineer

Jurupa Valley, CA · On-site

$81K - $110K/yr

Project coordination - Maintain continuous communication with sales, engineering, manufacturing ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Crane Company

Project Engineer

Jurupa Valley, CA · Hybrid

$81K - $110K/yr

Project coordination - Maintain continuous communication with sales, engineering, manufacturing ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Conagra Brands

Project Engineer

Oakdale, CA

$64K - $95K/yr

Reporting to the Plant Engineering Manager, you will provide project leadership and direction for ... Experience in food manufacturing, food processing, pharmaceutical manufacturing, or a related ...

Conagra Brands, Inc.

Project Engineer

Oakdale, CA · On-site

$64K - $95K/yr

Reporting to the Plant Engineering Manager, you will provide project leadership and direction for ... Experience in food manufacturing, food processing, pharmaceutical manufacturing, or a related ...

Lancesoft

Project Engineer 2

Vacaville, CA · On-site

$60 - $62.73/hr

... pharmaceutical environments. Key Responsibilities Technical & Engineering * Design, review, and modify HVAC systems, including: * Air Handling Units (AHUs), ducting, and airflow systems * Heating ...

Techoundsllc

Structural Project Engineer

Santa Barbara, CA

$89K - $119K/yr

... Senior Project Engineers and Project Managers. Candidates should possess strong analytical ... Pharmaceutical reimbursement * Professional affiliation reimbursement * Professional licensure ...

Techoundsllc

$83K - $111K/yr

... Senior Project Engineers and Project Managers. Candidates should possess strong analytical ... Pharmaceutical reimbursement * Professional affiliation reimbursement * Professional licensure ...

Techoundsllc

$83K - $111K/yr

... Senior Project Engineers and Project Managers. Candidates should possess strong analytical ... Pharmaceutical reimbursement * Professional affiliation reimbursement * Professional licensure ...

MYR Group

EPC Project Engineer

Santa Fe Springs, CA · On-site

$36/hr

ABOUT THE ROLE The Project Engineer will be responsible for coordinating with individuals, managing ... We are a trusted contractor to diverse industries, such as aerospace, biotech/pharmaceutical ...

MYR Group

EPC Project Engineer

Santa Fe Springs, CA · On-site

ABOUT THE ROLE The Project Engineer will be responsible for coordinating with individuals, managing ... We are a trusted contractor to diverse industries, such as aerospace, biotech/pharmaceutical ...

System One

Project Engineer III

Fremont, CA · On-site

$90 - $100/hr

Onsite Hours: 40.0 Overview A leading pharmaceutical company is seeking an experienced Project Engineer III to support engineering initiatives across Bulk Drug Substance (BDS), Drug Product (DP), and ...

System One

Project Engineer III

Fremont, CA · On-site

$90 - $100/hr

Onsite Hours: 40.0 Overview A leading pharmaceutical company is seeking an experienced Project Engineer III to support engineering initiatives across Bulk Drug Substance (BDS), Drug Product (DP), and ...

System One

Project Engineer III

Fremont, CA · On-site

$90 - $100/hr

Onsite Hours: 40.0 Overview A leading pharmaceutical company is seeking an experienced Project Engineer III to support engineering initiatives across Bulk Drug Substance (BDS), Drug Product (DP), and ...

System One

Project Engineer III

Fremont, CA · On-site

$90 - $100/hr

Onsite Hours: 40.0 Overview A leading pharmaceutical company is seeking an experienced Project Engineer III to support engineering initiatives across Bulk Drug Substance (BDS), Drug Product (DP), and ...

System One

Project Engineer III

Fremont, CA · On-site

$90 - $100/hr

Onsite Hours: 40.0 Overview A leading pharmaceutical company is seeking an experienced Project Engineer III to support engineering initiatives across Bulk Drug Substance (BDS), Drug Product (DP), and ...

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Pharmaceutical Project Engineer information

What engineers make $300,000 a year?

Senior pharmaceutical project engineers with extensive experience, advanced degrees, and specialized skills in project management and regulatory compliance can earn $300,000 or more annually. High compensation is often associated with leadership roles, large-scale projects, or working in highly regulated industries like pharmaceuticals.

What does a Pharmaceutical Engineer do?

A Pharmaceutical Engineer designs, develops, and optimizes manufacturing processes for drug production, ensuring compliance with safety and quality standards. They work with equipment, process validation, and regulatory requirements, often using tools like process simulation software and adhering to Good Manufacturing Practices (GMP).

What engineers make $500,000?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. These roles typically require advanced skills, extensive experience, and sometimes professional certifications or advanced degrees.

What is the difference between Pharmaceutical Project Engineer vs Pharmaceutical Manufacturing Specialist?

AspectPharmaceutical Project EngineerPharmaceutical Manufacturing Specialist
CredentialsBachelor's in Engineering, Project Management certificationsTechnical degree, GMP training, certifications in manufacturing processes
Work EnvironmentEngineering offices, labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical manufacturing facilities, contract manufacturers
Primary FocusPlanning, executing, and managing engineering projectsEnsuring manufacturing processes meet quality and compliance standards

The Pharmaceutical Project Engineer focuses on managing engineering projects within pharmaceutical companies, overseeing design, installation, and process improvements. In contrast, the Pharmaceutical Manufacturing Specialist concentrates on the day-to-day operations of manufacturing processes, ensuring quality and compliance. Both roles are essential in pharmaceutical production but differ in scope and responsibilities.

How does a Pharmaceutical Project Engineer typically collaborate with cross-functional teams during a project lifecycle?

Pharmaceutical Project Engineers work closely with cross-functional teams, including quality assurance, regulatory affairs, production, and R&D, to ensure that projects meet industry standards and compliance requirements. They often facilitate communication between departments, manage timelines, and coordinate technical solutions to address challenges that arise. This collaborative approach is key to delivering projects on time while adhering to strict safety and regulatory guidelines. Effective teamwork and communication skills are essential, as engineers must align diverse stakeholders and maintain project momentum.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior roles such as Pharmaceutical Vice Presidents, Directors of R&D, and Chief Scientific Officers tend to be the highest paid. These positions require extensive experience, advanced degrees, and leadership skills, often offering salaries exceeding $150,000 annually, with some executive roles earning significantly more.

What does a Pharmaceutical Project Engineer do?

A Pharmaceutical Project Engineer is responsible for planning, coordinating, and overseeing engineering projects within pharmaceutical manufacturing or research facilities. Their work includes designing and implementing new production processes, managing equipment installations, ensuring compliance with industry regulations, and optimizing operations for efficiency and safety. They often collaborate with cross-functional teams such as quality assurance, validation, and production to make sure projects are completed on time and within budget.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Project Engineer, and why are they important?

To thrive as a Pharmaceutical Project Engineer, you need a solid background in engineering (usually a degree in chemical, mechanical, or process engineering), combined with knowledge of pharmaceutical manufacturing processes and regulatory standards. Familiarity with project management software, CAD tools, and validation protocols, along with certifications like PMP or Six Sigma, is often required. Excellent problem-solving, communication, and teamwork skills help manage cross-functional teams and address complex project challenges. These skills and qualifications are crucial to ensure projects are delivered efficiently, safely, and in compliance with industry regulations.
What are popular job titles related to Pharmaceutical Project Engineer jobs in California? For Pharmaceutical Project Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Project Engineer jobs in California look for? The top searched job categories for Pharmaceutical Project Engineer jobs in California are:
Pharmaceutical Project Engineer jobs near you
Infographic showing various Pharmaceutical Project Engineer job openings in California as of July 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution.

Pharmaceutical Project Coordinator

TekWissen LLC

Vacaville, CA • On-site

$35 - $45/hr

Temporary

Posted 6 days ago

Job description

Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.

Job Title:       Project Coordinator – Change Control & Technology Transfer
Location:       Vacaville, CA 95688
Duration:       6 Months
Job Type:       Temporary Assignment        
Work Type:    Onsite

Summary:

We are seeking a Project Coordinator – Change Control & Technology Transfer / Project Administrator to support Technology Transfer and CAPEX projects within a GMP-regulated biopharmaceutical environment. This role is responsible for coordinating and managing Change Controls from initiation through closure, ensuring timely approvals, compliant execution, accurate documentation, and successful implementation of project deliverables. The Project Administrator will work closely with Project Managers and cross-functional teams to drive Change Control execution, monitor timelines, coordinate project activities, support stakeholder communications, and maintain audit-ready records while ensuring compliance with cGMP and site quality procedures.

Responsibilities:

  • Manage and coordinate Change Controls supporting Technology Transfer and CAPEX projects.
  • Drive Change Controls through the full lifecycle, including initiation, review, approval, implementation, and closure.
  • Monitor project and Change Control timelines, identify risks or delays, and escalate issues when necessary.
  • Coordinate activities with Quality, Manufacturing, Engineering, Validation, Regulatory, and Supply Chain teams.
  • Schedule and facilitate project meetings, prepare meeting minutes, and track action items to completion.
  • Support Project Managers with project planning, status tracking, milestone management, and cross-functional coordination.
  • Maintain project documentation and provide regular updates on project and Change Control status.
  • Assist with project reporting, milestone tracking, and stakeholder communications.
  • Ensure Change Controls and project documentation comply with site procedures, quality systems, and cGMP requirements.
  • Maintain accurate, complete, and audit-ready records.
  • Support inspection readiness and regulatory compliance activities.
  • Drive accountability across stakeholder groups to meet project timelines and business objectives.
  • Support continuous improvement of Change Control and project coordination processes.

Required Skills

  • Bachelor’s degree in Life Sciences, Biotechnology, Engineering, Quality, Business, or a related discipline preferred.
  • Minimum 2 years of experience in biotechnology, pharmaceutical, medical device, or other GMP-regulated industries.
  • Experience managing or coordinating Change Controls in a regulated environment.
  • Hands-on experience with electronic Quality Management Systems (eQMS) and Change Control platforms such as Veeva, TrackWise, MasterControl, or similar systems preferred.
  • Strong understanding of Change Control processes, quality systems, and regulated documentation practices.
  • Knowledge of cGMP requirements and regulated manufacturing environments.
  • Excellent organizational and time management skills.
  • Strong verbal and written communication skills.
  • Effective stakeholder management and cross-functional coordination abilities.
  • Ability to manage multiple priorities and drive actions to completion in a fast-paced environment.
  • Strong attention to detail and documentation accuracy.
  • Experience supporting Quality Assurance, Compliance/Quality Systems, Biotech or Pharmaceutical Manufacturing, Engineering, Validation, Technology Transfer, Project Administration, or Project Coordination activities preferred.
  • Proficiency in Microsoft Office applications, including Excel, Word, PowerPoint, and Outlook.
  • Ability to maintain confidential and compliant project records and support audit and inspection readiness activities.

TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.


TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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