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Chemical Technologies Jobs in Puerto Rico (NOW HIRING)

Veg Group

Sr. Manufacturing Engineer

Humacao, PR · On-site

$100 - $125/hr

... Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance ... and technology alongside a purpose-driven, supportive team. Validation & Engineering Group is an ...

Weil Group, Inc.

Process Engineer I

Humacao, PR · On-site

Mechanical, Biomedical, Industrial or Chemical Engineering Years' Experience Required: 3 ... The majority of time is spent delivering R&D, systems or initiatives related to new technologies or ...

Weil Group, Inc.

Process Engineer I

Humacao, PR · On-site

Mechanical, Biomedical, Industrial or Chemical Engineering Years' Experience Required: 3 ... The majority of time is spent delivering R&D, systems or initiatives related to new technologies or ...

Weil Group, Inc

Process Engineer I

Humacao, PR

Mechanical, Biomedical, Industrial or Chemical Engineering Years' Experience Required: 3 ... The majority of time is spent delivering R&D, systems or initiatives related to new technologies or ...

Weil Group, Inc

Process Engineer I

Humacao, PR

Mechanical, Biomedical, Industrial or Chemical Engineering Years' Experience Required: 3 ... The majority of time is spent delivering R&D, systems or initiatives related to new technologies or ...

Mirus Consulting Group

Chemist

Dorado, PR · On-site

$60 - $80/hr

... technology consulting services to pharmaceutical companies and other organizations across the ... Perform chemical and analytical testing of samples in accordance with established procedures and ...

Pinnaql

Sr. Manufacturing Engineer

Punta Santiago, PR · On-site

$90K - $123K/yr

... Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance ... are and technology alongside a purpose-driven, supportive team. Excited to build something ...

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All JobsChemical Technologies JobsChemical Technologies Jobs in Puerto Rico

Chemical Technologies information

What is the difference between Chemical Technologies vs Chemical Technicians?

AspectChemical TechnologiesChemical Technicians
Required CredentialsBachelor's degree in chemistry or related fieldAssociate's degree or diploma in chemical technology
Work EnvironmentResearch labs, manufacturing plants, quality controlLaboratories, production facilities, field sites
Employer & Industry UsageResearch & development, process design, technical supportTesting, data collection, process monitoring

Chemical Technologies professionals typically hold a bachelor's degree and focus on research, development, and technical support in various industries. Chemical Technicians usually have an associate's degree and assist in testing, data collection, and process monitoring. Both roles are essential in chemical industries but differ in education level and specific responsibilities.

What are popular job titles related to Chemical Technologies jobs in Puerto Rico?

For Chemical Technologies jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Chemical Technologies jobs in Puerto Rico look for?

The top searched job categories for Chemical Technologies jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Chemical Technologies jobs?

Cities in Puerto Rico with the most Chemical Technologies job openings:

Chemical Technologies jobs near you
Infographic showing various Chemical Technologies job openings in Puerto Rico as of June 2026, with employment types broken down into 92% Full Time, 5% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Validation Specialist (Cleaning-In-Place)

Veg Group

Humacao, PR • On-site

$80 - $100/hr

Other

Posted 19 days ago

Job description

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Specialist - CIP
Summary

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.

Key Responsibilities Commissioning & Qualification Execution
  • Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
  • Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
  • Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
  • Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity.
Documentation & Compliance
  • Generate and review URS, FAT/SAT, IOQ, and PQ documentation in compliance with ASTM E2500 and GAMP 5.
  • Ensure traceability from design specifications through executed testing.
  • Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
  • Prepare summary reports for Quality Assurance approval.
Cross-functional Collaboration
  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
  • Support operations during process validation batches and cleaning validation campaigns.
  • Provide training and technical guidance to CQV engineers and contractors executing test protocols.
Qualifications
  • Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
  • Experience in generating and executing documentation for CQV activities.
  • Strong knowledge of cleaning validation, sterilization principles, and automation integration.
  • Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
  • Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
  • Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
  • Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
  • Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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