Top 74 Chemical engineer Jobs in Puerto Rico

Process Development Sr. Scientist – Biopharmaceutical Manufacturing
PRPDG —Juncos, PR
- $55 - $60 an hour
- Full-time
- 5 years
- 3 years
- Bachelor's degree
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6d
Engineer
Weil Group, Inc —Juncos, PR
- Temporary
- Bilingual
- Computer literacy
- Engineering
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17h
Principal Process Scientist
Weil Group, Inc —Manatí, PR
- Temporary
- Background check
- Master's degree
- Bachelor's degree
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13d
Process Development Scientist
CMM Validation & Engineering Solutions, LLC. —Juncos, PR
- $48 - $50 an hour
- Full-time
- Doctoral degree
- Mid-level
- Master's degree
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Senior Engineer
Amgen —Municipio de Juncos, PR
- $115,494.60 - $156,257.40 a year
- Master's degree
- High school diploma or GED
- Doctor of Philosophy
- Disability insurance
- Health insurance
Process Development Scientist – Cell Sciences and Engineering
Amgen —Municipio de Juncos, PR
- On call
- Spanish
- Doctoral degree
- Laboratory experience
- Disability insurance
- Health insurance
Technical Applications Engineer (REMOTE) - Specialty Chemicals
Michael Page —Carolina, PR
- $80,000 - $120,000 a year
- Remote
- Spanish
- Mid-level
- Bachelor's degree
3d
Process Development Scientist
Cencora —Juncos, PR
- Full-time
- Spanish
- Word processing
- Computer literacy
- Paid parental leave
- Health insurance
Senior Scientist New Product Introduction
Biosimilar Sciences PR LLC —Aguadilla, PR
- Extended hours
- 5 years
- Office
- Analysis skills
- Dental insurance
- Vision insurance
Quick Apply
Principal Process Scientist
JC Automation Corp —Manatí, PR
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
Quick Apply
Senior Process Engineer
InnovaWorkforce Inc. —Juncos, PR
- $48 - $51 an hour
- 8 hour shift
- Doctoral degree
- Computer literacy
- Engineering
Quick Apply
Engineer
Validation & Engineering Group —Juncos, PR
- Full-time
- Engineering
- Research
- Mid-level
Quick Apply
Project Validation Specialist II - 60622 (Añasco)
One Group —Añasco, PR
- Extended hours
- Background check
- Spanish
- OSHA
Quick Apply
Process Engineer
BioPharma Consulting JAD Group —Carolina, PR
- Contract
- Spanish
- Doctoral degree
- Engineering
Quick Apply
Parenteral Process Scientist or Engineer
Validation & Engineering Group —Municipio de Juncos, PR
- Spanish
- Engineering
- English
Quick Apply
Engineer
Flexible & Integrated Technical Services, LLC —Carolina, PR
- Spanish
- Customer service
- Engineering
Quick Apply
Process Engineer I
Flexible & Integrated Technical Services, LLC —Humacao, PR
- Spanish
- Customer service
- English
Quick Apply
Engineer
CMM Validation & Engineering Solutions, LLC. —Juncos, PR
- $28 - $30 an hour
- Extended hours
- Spanish
- Engineering
- English
Quick Apply
Process Engineer
SOLX HOLDINGS LLC —Aguadilla, PR
- Mid-level
- 3 years
- Analysis skills
Quick Apply
CLEANING VALIDATION ENGINEER OR SPECIALIST
Validation & Engineering Group —Humacao, PR
- Full-time
- 5 years
- Engineering
- Senior level
Quick Apply

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Process Development Sr. Scientist – Biopharmaceutical Manufacturing

PRPDG
Juncos, PR

Quick Apply

Job Details

Full-time
$55 - $60 an hour
6 days ago

Qualifications

Biotechnology
Statistics
Content creation for technical audiences
Technical documentation
Quality control statistical data analysis
Contamination control
Technical writing experience within manufacturing
Biotechnology
GMP
Project management experience in manufacturing
Manufacturing facility experience
Sterile field contamination management
Production validation processes
Bachelor's degree
Pharmaceutical company experience
Scientific protocols
Quality assurance experience within pharmaceutical industry
Sterile products production
Statistical analysis tools
Pharmaceutical manufacturing facility experience
Scientific reports

Full Job Description

We are seeking a highly motivated Process Development Sr. Scientist to support process development, characterization, validation, and manufacturing readiness activities within a highly regulated pharmaceutical/biotechnology environment.

The ideal candidate will have strong experience supporting technical investigations, process improvements, validation activities, and data-driven decision-making to enable robust and compliant manufacturing processes.

Key Responsibilities:

Support process characterization studies, process validation activities, and continuous process improvement initiatives.
Analyze manufacturing data, identify process trends, and provide scientifically sound recommendations.
Develop and execute validation protocols, characterization studies, technical reports, investigations, and change controls.
Support technology transfer activities and manufacturing process implementation.
Collaborate with Manufacturing, Quality, Engineering, Regulatory, and Technical Services teams.
Apply statistical analysis and data-driven approaches to optimize process performance.
Provide technical support for commercial manufacturing readiness and process improvements.

Required Qualifications:

Doctorate (PhD, PharmD, or MD) with relevant experience; or Master’s degree with 3+ years of relevant scientific experience; or Bachelor’s degree with 5+ years of relevant scientific experience.
Degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess Engineering, Pharmaceutical Sciences, Biotechnology, Biology, Microbiology, or related scientific discipline preferred.
Experience in FDA/GMP-regulated pharmaceutical or biotechnology manufacturing environments.
Experience with process validation (PPQ), process characterization, technical documentation, and manufacturing support.
Strong knowledge of GMP requirements, aseptic processing principles, contamination control strategies, and pharmaceutical quality systems.
Experience with statistical analysis tools such as JMP or Minitab.
Strong technical writing, communication, and project management skills.
Ability to manage multiple priorities in a fast-paced manufacturing environment.
Sterile drug product manufacturing support.
Aseptic filling operations and filling equipment experience.
Single-use technologies and sterile manufacturing operations.
Experience authoring validation protocols, technical reports, investigations, and change controls.

If you have experience in process development, validation, GMP manufacturing, and scientific problem-solving, we encourage you to apply and join a team focused on advancing innovative healthcare solutions.

Job Type: Full-time

Pay: $55.00 - $60.00 per hour

Education:

Bachelor's (Preferred)

Experience:

pharmaceutical quality systems: 5 years (Preferred)
statistical analysis tools such as JMP or Minitab: 5 years (Preferred)
Sterile drug product manufacturing support: 5 years (Preferred)
Aseptic filling operations and filling equipment : 5 years (Preferred)
sterile manufacturing operations: 5 years (Preferred)
authoring validation protocols: 5 years (Preferred)
Change Control and Investigation: 5 years (Preferred)
FDA/GMP-regulated pharmaceutical or biotechnology : 5 years (Preferred)
process validation (PPQ): 5 years (Preferred)
process characterization: 5 years (Preferred)
technical documentation: 5 years (Preferred)
manufacturing support: 5 years (Preferred)
aseptic processing principles: 5 years (Preferred)
contamination control strategies: 5 years (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

chemical engineer jobs in puerto rico

Process Development Sr. Scientist – Biopharmaceutical Manufacturing

Engineer

Principal Process Scientist

Process Development Scientist

Senior Engineer

Process Development Scientist – Cell Sciences and Engineering

Technical Applications Engineer (REMOTE) - Specialty Chemicals

Process Development Scientist

Senior Scientist New Product Introduction

Principal Process Scientist

Senior Process Engineer

Engineer

Project Validation Specialist II - 60622 (Añasco)

Process Engineer

Parenteral Process Scientist or Engineer

Engineer

Process Engineer I

Engineer

Process Engineer

CLEANING VALIDATION ENGINEER OR SPECIALIST

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