Top 145 Senior engineer Jobs in Fajardo Pr

Process Development Sr. Scientist
PRPDG —Juncos, PR
- $55 - $60 an hour
- Weekends as needed
- 5 years
- Engineering
- Mid-level
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3d
Senior Engineer
Amgen —Municipio de Juncos, PR
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- Master's degree
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Kenvue —Las Piedras, PR
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T & T Management Group —Juncos, PR
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CMM Validation & Engineering Solutions, LLC. —Juncos, PR
- $50 - $52 an hour
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InnovaWorkforce Inc. —Juncos, PR
- $48 - $51 an hour
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Sr. Engineer 35409
Inteldot —Municipio de Juncos, PR
- Full-time
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Senior Engineering Scientist
Kenvue —Las Piedras, PR
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- Spanish
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Sr Engineer
Cencora —Juncos, PR
- Full-time
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Senior Process Engineer
BioPharma Consulting JAD Group —Juncos, PR
- Contract
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3d
Sr. Engineer
PRPDG —Juncos, PR
- $45 - $50 an hour
- Full-time
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- 5 years
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35534 - Process Development Sr Scientist-aseptic filling, process validation, technology transfer
BES Consulting Group, LLC —Juncos, PR
- $55 - $60 an hour
- Weekends as needed
- Bilingual
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- Medicine
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Process Development Sr. Scientist – Biopharmaceutical Manufacturing
PRPDG —Juncos, PR
- $55 - $60 an hour
- Full-time
- 5 years
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Sr Supplier Quality Engineer
Weil Group, Inc —Juncos, PR
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Process Development Sr Scientist
Weil Group, Inc —Juncos, PR
- Temporary
- Background check
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3d
Sr. Engineer
Weil Group, Inc —Juncos, PR
- Temporary
- Background check
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Sr. Engineer
Weil Group, Inc —Juncos, PR
- Temporary
- Bilingual
- Background check
- Computer literacy
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Sr. Engineer
Weil Group, Inc —Juncos, PR
- Temporary
- Background check
- Doctoral degree
- Computer literacy
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Sr Engineer
PRPDG —Municipio de Juncos, PR
- Full-time
- Management
- Doctoral degree
- Engineering
Sr. Engineer
Biopharma Consulting Services —Juncos, PR
- From $48 an hour
- Full-time
- Spanish
- Doctoral degree
- Engineering
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3d

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senior engineer jobs near fajardo pr

Process Development Sr. Scientist

PRPDG
Juncos, PR

Quick Apply

Job Details

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

Qualifications

Bachelor's degree

Full Job Description

We are seeking a Process Development Sr. Scientist to support process development, process validation, technical documentation, and manufacturing support activities within a highly regulated manufacturing environment. This position offers the opportunity to work in a cross-functional setting, contributing to process improvements, validation initiatives, and commercial manufacturing readiness while ensuring compliance with quality and regulatory requirements.

Responsibilities

Support process development, process characterization, and process validation activities.
Author, review, and execute validation protocols, technical documentation, and validation reports.
Support equipment qualification and validation activities in compliance with GMP requirements.
Analyze process performance data, identify trends, and recommend process improvements using scientific and risk-based approaches.
Collaborate with Manufacturing, Quality, Engineering, and other cross-functional teams to support manufacturing readiness and process optimization.
Participate in investigations, root cause analysis, CAPA activities, and implementation of corrective actions.
Support change control activities and technical documentation updates.
Contribute to continuous improvement initiatives that enhance process robustness, compliance, and operational efficiency.
Support manufacturing operations during validation, characterization, and other critical production activities, including flexibility to work alternate shifts or weekends when required.

Qualifications

Doctorate (PhD, PharmD, or MD); OR Master's degree with 3+ years of relevant scientific experience; OR Bachelor's degree with 5+ years of relevant scientific experience.
Degree in Engineering, Microbiology, or another related scientific discipline.
Experience supporting validation activities in a highly regulated manufacturing environment.
Experience developing and/or executing validation protocols and technical documentation.
Knowledge of GMP requirements and quality systems.
Strong analytical, technical writing, and problem-solving skills.
Ability to work independently while collaborating effectively with cross-functional teams.
Willingness to work different shifts and weekends during characterization or validation activities.
Experience supporting pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
Experience with process monitoring, process characterization, and continuous improvement initiatives.
Knowledge of statistical tools such as Minitab or similar software.
Experience with risk management methodologies and data analysis.
Strong communication, organizational, and project management skills.

If you are passionate about process development, validation, and scientific problem-solving in a regulated manufacturing environment, we encourage you to apply.

Job Type: Full-time

Pay: $55.00 - $60.00 per hour

Education:

Bachelor's (Preferred)

Experience:

supporting validation activities: 5 years (Preferred)
developing and/or executing validation protocols: 5 years (Preferred)
GMP requirements and quality systems: 5 years (Preferred)
characterization: 5 years (Preferred)
supporting pharmaceutical, biotechnology, medical device: 5 years (Preferred)
process monitoring: 5 years (Preferred)
statistical tools such as Minitab or similar software: 5 years (Preferred)
risk management methodologies: 5 years (Preferred)
data analysis: 5 years (Preferred)

Work Location: In person

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Refine Your Search

senior engineer jobs in fajardo pr

Process Development Sr. Scientist

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35534 - Process Development Sr Scientist-aseptic filling, process validation, technology transfer

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