ZipRecruiter

Log In

1

Pharmaceutical Project Engineer Jobs in California

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 ...

RadNet, Inc.

Senior Project Engineer

San Leandro, CA · On-site

$117.77 - $153.08/hr

The Senior Project Engineer manages capital improvement projects to build, maintain, and improve ... Food or pharmaceutical background preferred; Chocolate experience desired * Ability to effectively ...

PM Group

Senior Project Engineer

Van Nuys, CA · On-site

$103K - $134K/yr

Overview The Senior Project Engineer position is an exciting opportunity to join PM Group's quickly ... Pharmaceutical, Biopharmaceutical, Cell & Gene Therapy sectors) * Experience managing capital ...

PM Group

Senior Project Engineer

Van Nuys, CA · On-site

$103K - $134K/yr

Overview The Senior Project Engineer position is an exciting opportunity to join PM Group's quickly ... Pharmaceutical, Biopharmaceutical, Cell & Gene Therapy sectors) * Experience managing capital ...

Concuir, Inc

Project Engineer II to III

San Diego, CA · On-site

$90K - $110K/yr

Consultant - Project Engineer II through III Compensation package annual salary is ($90,000 - $110 ... pharmaceutical and/or biotech manufacturing clients. In this role, you will quickly learn common ...

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

Consultant - Project Engineer II through III Compensation package annual salary is ($90,000 - $110 ... pharmaceutical and/or biotech manufacturing clients. In this role, you will quickly learn common ...

Concuir, Inc

Project Engineer II to III

San Diego, CA · On-site

$90K - $110K/yr

Consultant - Project Engineer II through III Compensation package annual salary is ($90,000 - $110 ... pharmaceutical and/or biotech manufacturing clients. In this role, you will quickly learn common ...

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

Consultant - Project Engineer II through III Compensation package annual salary is ($90,000 - $110 ... pharmaceutical and/or biotech manufacturing clients. In this role, you will quickly learn common ...

Concuir, Inc

Project Engineer II to III

San Diego, CA · On-site

$90K - $110K/yr

Consultant - Project Engineer II through III Compensation package annual salary is ($90,000 - $110 ... pharmaceutical and/or biotech manufacturing clients. In this role, you will quickly learn common ...

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

Consultant - Project Engineer II through III Compensation package annual salary is ($90,000 - $110 ... pharmaceutical and/or biotech manufacturing clients. In this role, you will quickly learn common ...

previous pagenext page

Showing results 21-40

All JobsPharmaceutical Project Engineer JobsPharmaceutical Project Engineer Jobs in California

Pharmaceutical Project Engineer information

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 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 August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution.

Project Engineer III

System One

Fremont, CA • On-site

$90 - $100/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 24 days ago

Job description

Job Title: Project Engineer III Location: Fremont, CA Type: Contract Compensation: $90-100/hr Contractor Work Model: 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 Process Science (PS) systems. The ideal candidate will bring strong technical expertise in GMP manufacturing environments, hands-on process equipment experience, and proven project leadership capabilities within biopharmaceutical operations. Responsibilities

  • Serve as the Engineering technical lead for Bulk Drug Substance (BDS), Drug Product (DP), and/or Process Science (PS) systems. This includes but is not limited to Upstream and Downstream BDS, Filling and Packaging equipment.
  • Serve as a primary consultant to troubleshoot equipment/process issues through initial qualification and system release, support/participate/lead site CAPEX/OPEX/continuous improvement projects from feasibility study to handover.
  • Might also own change control and participate in deviation/risk assessment activities.
  • Manage medium in size and complexity equipment related projects.
  • Expected to act as System Owner for Process equipment (out of tolerance events, deviations, etc.) if required by area.
  • Uses expert knowledge about the processes, automation and process-specific technology to participate in troubleshooting as the Engineering technical lead.
  • Technical Analysis: including process system and technology plant fits, capacity and equipment utilization, value engineering, sustainable design, constructability and assessment of applicable new technologies to balance performance, cost and maintainability.
  • Lead/participate in CAPEX/OPEX/CI projects.
  • Own risk assessment for new systems and changes to existing systems.
  • Write/review project execution plans.
  • Lead/manage startup/commissioning activities (e.g. approve commissioning report, review/approve TOPs, create/update/review/approve SOPs...)
  • Technical approvers of protocols and periodic monitoring.
  • Lead/manage project team including overseeing & providing guidance on contractors activities.
  • Provides estimates of resource requirements.
  • Own technical optimization of the field of care.
  • Ensures that the facility equipment, machinery, documentation and technical support meet the compliance, quality and EHS standards.
  • Leads/motivates activities to ensure a continuous optimization process.
  • Leads/execute CAPA, deviation, change control, and risk assessment (quality, business and/or safety).
  • Leads implementation and improvement of best practice of technical standards, procedures.
  • Acts as a member of Global Engineering Biopharmaceuticals and of global Engineering.
  • Participates in peer-to-peer reviews as needed.
  • Collaborate with internal cross functional groups - Mfg, SCM, Quality, CMO, Finance, IT.
  • Work closely with external contingency worker, contractors, possible customers, auditor.
Requirements
  • Bachelor’s in Engineering, 5-10 years of related field experience or, Master’s in Engineering, +5 years’ of related field experience or P.E. License.
  • Minimum of 4 years’ working experience in a GMP manufacturing environment.
  • Minimum 5 years and hands on experience with process system/equipment.
  • Regulatory requirement per GMP, OSHA and FDA.
  • Knowledge of GMP compliance.
  • Technical expertise on process equipment/system.
  • Recognize safety requirements in manufacturing environment.
  • Equipment hands on experience.
  • Project leadership experience.
  • Capable to own and lead risk assessment, root cause investigation, project startup/commissioning/qualification.
  • Expert on troubleshooting technical issues.
  • Owner of change control, deviation and CAPA.
  • Capable to lead projects (CAPEX or CI).
  • Capable of balance conflicting priorities and agile to manage changing priorities.
  • Ability to establish highly functional relationships with diverse personalities.
  • Physical demands/surroundings - work primarily in an office environment. Required to be on the process floor as necessary to perform work outlined in this profile.
  • Some domestic and international travel may be required.
  • Visual Demands - must be able to read and see clearly with or without correction lenses.
  • Excellent oral and written communication skills.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Ref: #558-Scientific