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Biotech Process Development Jobs (NOW HIRING)

We are seeking Process Development Engineers that will supports the development, validation, and ... Previous experience in regulated industry (Pharma, Biotech, or Medical Devices). * Experience with ...

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Biotech Process Development information

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$18

$33

$49

How much do biotech process development jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for biotech process development in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What are the key skills and qualifications needed to thrive in biotech process development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in biotech process development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

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What cities are hiring for Biotech Process Development jobs?

Cities with the most Biotech Process Development job openings:

What states have the most Biotech Process Development jobs?

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What are popular job titles related to Biotech Process Development jobs?

For Biotech Process Development jobs, the most frequently searched job titles are:

Infographic showing various Biotech Process Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Process Development Engineer

Dorado, PR • On-site

Other

Medical, Dental, Vision, Life, PTO

Posted 14 days ago


Job description

EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.

We are seeking Process Development Engineers that will supports the development, validation, and implementation of new manufacturing processes. The role involves documentation generation, process optimization, and cross-functional collaboration.

Responsibilities:

  • Perform process validation and equipment qualification activities / reports (IQ, OQ, PQ) and develop Master Validation Plans.

  • Generate equipment documentation (evaluations, PM/calibration procedures) and manufacturing instructions.

  • Design and develop in‑process and receiving inspection systems for new components and processes.

  • Characterize, optimize, and improve manufacturing processes through DOE, PFMEA, and risk analysis.

  • Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors).

Minimum Requirements:

  • Bachelor Degree in Engineering (Electrical and Mechanical backgrounds preferred).

  • Previous experience in regulated industry (Pharma, Biotech, or Medical Devices).

  • Experience with automated manufacturing system and equipment (laser welding, heat bonding, injection molding, vision systems).

  • Experience with automation/controls, tooling, fixtures, test method development.

  • Proficiency in DOE, FMEA, CAPA, and root‑cause investigation.

  • Good technical writing skills.

  • Fully bilingual (English and Spanish).

Benefits:

  • Health insurance (Medical, Dental, Vision, Pharmacy)

  • Life Insurance

  • Paid time off (PTO)

  • Holidays

  • Professional Growth (Courses and Certifications by EQVAL Academy)

  • Referral program

  • Productivity incentive

*This position will be full-time 100% on site in Puerto Rico.

We offer competitive compensation, benefits, and opportunities for career growth. If you are a motivated individual with passion, we would love to hear from you.

EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.

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