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Remote Gmp Manufacturing Jobs in Puerto Rico (NOW HIRING)

Kelly Services

Senior Validations Engineer

Juncos, PR · On-site +1

$45/hr

Administrative shift (support a 24/7 manufacturing operations, some remote work is possible) Why ... Strong understanding of GMP, FDA/EMA regulations, Data Integrity (ALCOA+), Change Controls ...

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Remote Gmp Manufacturing information

What is remote GMP manufacturing?

Remote GMP manufacturing refers to the oversight, management, or operation of Good Manufacturing Practice (GMP) compliant production processes from a location outside the actual manufacturing facility. This can involve remote monitoring of production data, quality control, and compliance activities using digital tools and secure communication platforms. The goal is to maintain high standards of product quality and regulatory compliance, even when staff or consultants are not physically present onsite. This approach has become more common due to advancements in technology and the increased need for flexibility in the pharmaceutical and biotechnology industries.

What are the key skills and qualifications needed to thrive as a remote GMP manufacturing professional?

To thrive as a Remote GMP Manufacturing professional, you need in-depth knowledge of Good Manufacturing Practices (GMP), quality control, and regulatory compliance, typically supported by a degree in life sciences or engineering. Familiarity with digital manufacturing systems, batch record management software, and possibly certifications like Six Sigma or GMP training is essential. Strong attention to detail, problem-solving skills, and effective remote communication set outstanding candidates apart. These skills ensure the integrity of product quality and regulatory compliance, even in a remote or decentralized work environment.

What are some common challenges of working in a remote GMP manufacturing role, and how can they be addressed?

Working remotely in GMP (Good Manufacturing Practice) manufacturing presents unique challenges, such as ensuring strict compliance with regulatory standards without being physically present on-site. Communication with on-site teams is crucial to maintain oversight and address any deviations or quality concerns promptly. Leveraging digital tools, clear documentation, and regular virtual meetings can help bridge the gap. It’s also important to stay updated on the latest regulatory changes and maintain strong collaboration with quality assurance, production, and validation teams to ensure all processes are followed accurately.

What is the difference between Remote Gmp Manufacturing vs Remote Quality Assurance?

AspectRemote Gmp ManufacturingRemote Quality Assurance
CredentialsGMP certifications, technical manufacturing experienceGMP certifications, quality control certifications
Work EnvironmentManufacturing facilities, labs, or remote production oversightRemote review, audits, documentation, and compliance checks
Industry UsagePharmaceutical, biotech, and medical device manufacturingPharmaceutical, biotech, and medical device industries
Common Search IntentManufacturing processes, production oversightQuality compliance, audits, documentation

Remote Gmp Manufacturing focuses on overseeing and managing manufacturing processes remotely, ensuring production meets GMP standards. Remote Quality Assurance emphasizes maintaining quality compliance through remote audits, reviews, and documentation. Both roles require GMP certifications but differ in daily tasks and focus areas within the industry.

What are popular job titles related to Remote Gmp Manufacturing jobs in Puerto Rico?

For Remote Gmp Manufacturing jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Remote Gmp Manufacturing jobs in Puerto Rico look for?

The top searched job categories for Remote Gmp Manufacturing jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Remote Gmp Manufacturing jobs?

Cities in Puerto Rico with the most Remote Gmp Manufacturing job openings:

Remote Gmp Manufacturing jobs near you
Infographic showing various Remote Gmp Manufacturing job openings in Puerto Rico as of June 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 100% Remote job distribution.

Senior Validations Engineer

Kelly Services

Juncos, PR • On-site, Remote

$45/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Key responsibilities

  • Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.

  • Oversee and/or execute commissioning activities including FAT, SAT, and field commissioning.

  • Author, review, and approve qualification protocols (IQ, OQ, PQ).

Job description

At Kelly® Engineering  we’re passionate about helping you find a job that works for you. How about this one?
We’re seeking Senior Validations Engineer to work for one of our top Biotechnology Industry client at Juncos, PR. 
Salary: $45.00 hr - W2
Shift: Administrative shift (support a 24/7 manufacturing operations, some remote work is possible)
Why you should apply to be Senior Validations Engineer
  • Competitive pay with biweekly direct deposit (W-2)
  • Hands-on experience supporting critical manufacturing and quality systems in a leading biotechnology environment
  • Collaborative, fast-paced, and dynamic workplace with growth opportunities
  • Access to extensive training resources and career guidance
  • Paid vacation, sick leave, holidays, and eligibility for a Christmas bonus (Must comply with minimum established requirements to qualify.)
This job might be an outstanding fit if you have the following requirements: 
  • MS degree  in Engineering and 2 years of directly related experience OR BS degree in Engineering and 4 years of directly related experience in pharmaceutical, biotechnology, or other regulated manufacturing industrie
  • Experience leading Commissioning & Qualification (C&Q) strategies, planning, scheduling, and resource management in GMP environments.
  • Strong expertise in FAT, SAT, startup, field commissioning, and IQ/OQ/PQ execution.
  • Knowledge of ASTM E2500, ISPE guidance, risk assessments, and qualification lifecycle management.
  • Experience authoring, reviewing, and approving qualification protocols, validation reports, and technical documentation.
  • Strong understanding of GMP, FDA/EMA regulations, Data Integrity (ALCOA+), Change Controls, Deviations, and CAPA. 
  • Experience developing and executing process characterization studies, with strong technical writing, leadership, and project management skills.
  • Proficient in data analysis and strong technical writing skills in English and Spanish.
The Senior Validations Engineer will be responsible for; C&Q Strategy & Planning: Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements. Commissioning Activities: Oversee and/or execute commissioning activities including FAT, SAT, and field commissioning. Qualification Execution (IQ/OQ/PQ): Author, review, and approve qualification protocols (IQ, OQ, PQ). Documentation & Compliance: Ensure all C&Q documentation complies with GMP, FDA, EMA, and internal company standards. Risk Management & Change Control: Lead and document risk assessments related to system qualification. Evaluate and manage change controls impacting validated systems. Assess impact of deviations and implement corrective and preventive actions (CAPA). Cross-functional Coordination: Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams. Characterization Process: Develop the characterization protocols. Execute the characterization activities. Develop and review the characterization reports

Helping you discover what’s next in your career is what we’re all about, so let’s get to work.
Apply to be Senior Validations Engineer today!
Recruiter: Lilly Abouomar 9395454792 
#SETTPuertoRico
 


As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Engineering?

Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world’s most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we’re here to guide you to the next step in your engineering career.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
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