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Biotech Process Engineer Jobs in Menifee, CA (NOW HIRING)

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience as an engineer in the pump industry is preferred * Minimum of 5 years of experience ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

Dover Corporation

Engineering Manager

Grand Terrace, CA

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience as an engineer in the pump industry is preferred * Minimum of 5 years of experience ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience as an engineer in the pump industry is preferred * Minimum of 5 years of experience ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

Dover Corporation

Engineering Manager

Grand Terrace, CA

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience as an engineer in the pump industry is preferred * Minimum of 5 years of experience ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience as an engineer in the pump industry is preferred * Minimum of 5 years of experience ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

Glaukos

Sr. Engineering Technician

San Clemente, CA · On-site

Troubleshoot and resolve equipment and process-related issues on the production floor. * Support ... biotechnology. * At least 2 years of hands-on experience troubleshooting and supporting ...

Glaukos

Sr. Engineering Technician

San Clemente, CA · On-site

Troubleshoot and resolve equipment and process-related issues on the production floor. * Support ... biotechnology. * At least 2 years of hands-on experience troubleshooting and supporting ...

Glaukos

Sr. Engineering Technician

San Clemente, CA · On-site

Troubleshoot and resolve equipment and process-related issues on the production floor. * Support ... biotechnology. * At least 2 years of hands-on experience troubleshooting and supporting ...

JLL

Senior Facilities Manager

Oceanside, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead and mentor a team of facilities technicians and engineers, fostering a culture of ... Experience with validation protocols, qualification processes (IQ/OQ/PQ), and change control ...

Dover Corporation

CNC Programmer/Machinist

Grand Terrace, CA · On-site

$26.25 - $35.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biotech, Quantex, Quattroflow, and Wilden. PSG products are manufactured on three continents ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

Dover Corporation

CNC Programmer/Machinist

Grand Terrace, CA · On-site

$26.25 - $35.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

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Showing results 21-40

All JobsBiotech Process Engineer JobsBiotech Process Engineer Jobs in Menifee, CA

Biotech Process Engineer information

See Menifee, CA salary details

$52.4K

$97.4K

$150.8K

How much do biotech process engineer jobs pay per year?

As of Aug 15, 2026, the average yearly pay for biotech process engineer in Menifee, CA is $97,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,800.00 and $109,000.00 per year, depending on experience, location, and employer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

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

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are popular job titles related to Biotech Process Engineer jobs in Menifee, CA?

For Biotech Process Engineer jobs in Menifee, CA, the most frequently searched job titles are:

What cities near Menifee, CA are hiring for Biotech Process Engineer jobs?

Cities near Menifee, CA with the most Biotech Process Engineer job openings:

Biotech Process Engineer jobs near you
Infographic showing various Biotech Process Engineer job openings in Menifee, CA as of August 2026, with employment types broken down into 69% Full Time, and 31% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $97,362 per year, or $46.8 per hour.

Sterile Manufacturing Supervisor

K2 Staffing

Temecula, CA

Full-time

Re-posted 16 hours ago

Job description

Summary

We are seeking an experienced Sterile Filling Line Supervisor to lead clean room manufacturing operations within a fast-growing nutritional and pharmaceutical-grade production environment. This individual will play a critical role in overseeing sterile filling operations, ensuring equipment runs efficiently, production goals are achieved, and all activities comply with GMP, quality, and safety standards.
The ideal candidate will possess a strong background in sterile manufacturing, pharmaceutical, nutraceutical, biotechnology, medical device, or other regulated production environments. This is a hands-on leadership role responsible for setting up, operating, troubleshooting, and optimizing sterile filling equipment while supervising production personnel and maintaining the highest standards of product quality and regulatory compliance.

Duties & Responsibilities
  • Production & Equipment Operations
    • Set up, operate, monitor, and troubleshoot sterile filling and bottling equipment to ensure efficient and compliant production operations.
    • Perform equipment changeovers, adjustments, calibrations, and line clearances as required.
    • Ensure filling lines consistently meet production, quality, and efficiency targets.
    • Identify and resolve equipment, process, and operational issues to minimize downtime and maximize throughput.
    • Coordinate preventative maintenance activities and work closely with maintenance personnel to ensure equipment reliability.
    • Monitor production schedules and adjust staffing and resources as necessary to meet operational demands.
  • Leadership & Personnel Management
    • Supervise, train, coach, and develop production personnel assigned to sterile filling and bottling operations.
    • Ensure team members follow all Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs), and clean room protocols.
    • Conduct performance evaluations, provide ongoing feedback, and support employee development initiatives.
    • Foster a culture of accountability, teamwork, safety, and continuous improvement.
    • Assist with staffing decisions, onboarding, and training of new employees.
  • Quality & Compliance
    • Ensure all manufacturing activities comply with cGMP, FDA, OSHA, and company quality standards.
    • Review and maintain accurate batch records, production logs, and manufacturing documentation.
    • Verify completion of in-process inspections and quality checks throughout production activities.
    • Support internal audits, regulatory inspections, investigations, corrective actions, and continuous improvement initiatives.
    • Ensure strict adherence to aseptic processing, contamination control, and clean room procedures.
  • Operational Excellence
    • Monitor key performance indicators including throughput, yields, downtime, waste reduction, and labor efficiency.
    • Recommend and implement process improvements that increase productivity while maintaining product quality.
    • Collaborate with Quality Assurance, Quality Control, Warehouse, Planning, and Operations teams to support overall business objectives.
    • Maintain a clean, organized, and audit-ready manufacturing environment.
Qualifications & Requirements
  • Education
    • High School Diploma or GED required.
    • Associate's or Bachelor's degree in Engineering, Manufacturing, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field preferred.
  • Experience
    • Minimum of 5 years of manufacturing experience within a pharmaceutical, nutraceutical, biotechnology, medical device, cosmetic, or other regulated production environment.
    • Minimum of 2 years of supervisory or leadership experience overseeing production personnel.
    • Proven experience operating, setting up, troubleshooting, and optimizing filling, bottling, packaging, or related manufacturing equipment.
    • Experience working within clean room and sterile manufacturing environments strongly preferred.
    • Experience with aseptic processing and contamination control practices is highly desirable.
  • Technical Skills
    • Strong knowledge of GMP, cGMP, FDA, and quality system requirements.
    • Familiarity with batch records, manufacturing documentation, deviation reporting, and corrective actions.
    • Ability to diagnose and resolve mechanical, operational, and production issues.
    • Proficiency with manufacturing software systems and Microsoft Office applications.
    • Strong understanding of lean manufacturing principles and continuous improvement methodologies.
  • Leadership Competencies
    • Demonstrated ability to lead, motivate, and develop production teams.
    • Strong decision-making, problem-solving, and organizational skills.
    • Excellent communication and interpersonal abilities.
    • Ability to effectively manage multiple priorities in a fast-paced manufacturing environment.
  • Physical Requirements
    • Ability to stand, walk, bend, and perform production-related activities throughout the workday.
    • Ability to lift and move materials weighing up to 50 pounds.
    • Ability to wear required clean room attire, including gowns, gloves, masks, hairnets, and other personal protective equipment for extended periods.
  • Preferred Qualifications
    • Experience supervising sterile filling, bottling, packaging, or aseptic manufacturing operations.
    • Lean Manufacturing, Six Sigma, or Continuous Improvement training.
    • GMP, cGMP, or pharmaceutical manufacturing certifications.
    • Experience preparing for and participating in FDA, ISO, NSF, or customer audits.
Employment Type: Full time Location: Temecula, CA