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Biotech Process Development Jobs in Caguas, PR (NOW HIRING)

Mentor Technical Group

Engineer

Juncos, PR · On-site

... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Work with research, manufacturing, maintenance, process development, utilities, facilities, quality ...

BioPharma Consulting JAD Group

Engineer

Juncos, PR · On-site

... biotech/pharmaceutical environment. The engineer organizes, analyzes, and interprets operational ... Partner with manufacturing, maintenance, process development, utilities, facilities, quality ...

Weil Group, Inc.

Engineer

Juncos, PR · On-site

... process development, utilities, facilities, quality assurance and/or validation departments in ... pharmaceutical/biotech processes Familiarity with validation processes Familiarity with ...

Mirus Consulting Group

Engineer - 35388

Juncos, PR · On-site

Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance ... Knowledge of pharmaceutical or biotechnology processes and GMP operations * Strong organizational ...

Mirus Consulting Group

Engineer - 35388

Juncos, PR · On-site

Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance ... Knowledge of pharmaceutical or biotechnology processes and GMP operations * Strong organizational ...

Ultimate Solutions

Sr Engineer-Packaging

Juncos, PR · On-site

... biotechnology, medical devices and logistics markets. DESCRIPTION Independently provides and/or ... Work with research, manufacturing, process development, utilities, facilities, quality assurance ...

Weil Group, Inc.

Sr. Engineer

Juncos, PR · On-site

$102K - $140K/yr

... manufacturing, process development, utilities, facilities, quality assurance and validation ... biotech processes • Familiarity with validation processes • Familiarity with documentation in a ...

Ultimate Solutions

Sr Engineer

Juncos, PR · On-site

$101K - $139K/yr

Work with research, manufacturing, process development, utilities, facilities, quality assurance ... biotech processes • Familiarity with validation processes • Familiarity with documentation in a ...

Kelly Services

Principal Engineer

Juncos, PR

$53/hr

We're seeking a Principal Engineer to work at a premier pharmaceutical/biotechnology industry ... Collaborating with cross-functional teams, including research, manufacturing, process development ...

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All JobsBiotech Process Development JobsBiotech Process Development Jobs in Caguas, PR

Biotech Process Development information

See Caguas, PR salary details

$18

$32

$48

How much do biotech process development jobs pay per hour?

As of Jul 10, 2026, the average hourly pay for biotech process development in Caguas, PR is $32.85, according to ZipRecruiter salary data. Most workers in this role earn between $26.97 and $40.34 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 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.

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.
Biotech Process Development jobs near you
Process Development Engineer

Process Development Engineer

Weil Group, Inc.

Dorado, PR • On-site, Remote

Full-time

Re-posted 3 days ago

Job description

Role Summary
The Process Development Engineer supports the development, validation, and implementation of new manufacturing processes. The role involves equipment and process validation, documentation generation, process optimization, and cross-functional technical collaboration.
Key Responsibilities
  • Support IQ/OQ/PQ and process performance qualification activities; develop validation protocols, reports, and master validation plans.
  • Design and develop inprocess and receiving inspection systems for new components and processes.
  • Generate equipment documentation (evaluations, PM/calibration procedures) and manufacturing instructions.
  • Manage process development projects from concept through implementation; collaborate with cross-functional teams.
  • Apply DOE, PFMEA, and risk analysis to characterize, optimize, and improve manufacturing processes.
  • Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors).

Experience Requirements
  • 5-7+ years in manufacturing engineering or quality engineering within an FDAregulated environment (medical devices, pharma, diagnostics, biotech).
  • Strong working knowledge of 21 CFR Part 820, GMP, and ISO 13485.
  • Electrical and mechanical engineering background applied to automated manufacturing systems.
  • Experience with automation/controls, tooling, fixtures, test method development, and equipment qualification.
  • Proficiency in DOE, FMEA, CAPA, and rootcause investigation.
  • Experience supporting new product introductions and process scaleup.

Quality Expectations
Demonstrates commitment to patient safety and product quality by complying with all applicable quality procedures.
Ensures proper documentation discipline and supports Quality System compliance.
Special requirement:
  1. 3.00 GPA minimum
  2. RUM or Polytechnic University graduates
  3. BS in Engineering
**Weil Group is proud to be an Equal Employment Opportunity Employer.*

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