Top 27 Regulatory qa Jobs in Manatí Pr

Quality Assurance Specialist
Kelly Services —Barceloneta, PR
- Full-time
- Hybrid work
- Mid-level
- 3 years
- US work authorization
- Paid holidays
- Disability insurance
Quick Apply
QA / Documentation Specialist
Qualitech Management Solutions —Barceloneta, PR
- $20 - $40 an hour
- Part-time
- Background check
- Mid-level
- Bachelor's degree
Quick Apply
12d
Regulatory QA Specialist
HR Works —Barceloneta, PR
- $30 - $45 an hour
- Contract
- Senior level
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Quality Assurance (QA) Specialist II
Artech LLC —Barceloneta, PR
- $20.00 - $21.16 an hour
- Contract
- Bilingual
- Mid-level
- Manufacturing
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QA Specialist
PSC Biotech —Manatí Municipio, PR
- Full-time
- 5 years
- English
- US work authorization
7d
Senior IT Operations Support Specialist
Weil Group, Inc —Manatí Municipio, PR
- $334 a day
- Temporary
- Spanish
- 5 years
- Bachelor of Science
Quick Apply
2d
Computer System Validation (CSV) Specialist (EBR System)
Validation & Engineering Group, Inc —Barceloneta, PR
- Full-time
- 5 years
- Senior level
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Validation Engineer
Validation & Engineering Group, Inc —Barceloneta, PR
- Extended hours
- Engineering
- 3 years
- Senior level
Quick Apply
Project Manager - MES
Flexible & Integrated Technical Services, LLC —Manatí, PR
- Spanish
- Customer service
- Engineering
Quick Apply
Senior Quality Analyst
Validation & Engineering Group, Inc —Guaynabo, PR
- Full-time
- Mid-level
- 4 years
- Communication skills
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17h
Senior Project Manager - (PE License) - Construction
Custom Group, LLC. PR —Guaynabo, PR
- From $105,000 a year
- Full-time
- Spanish
- Writing skills
- English
- Health insurance
- 401(k)
Quick Apply
Project Manager - Air Quality
SWCA Environmental Consultants —United States
- $102,047.40 - $134,152.20 a year
- Online Application
- Remote
- 7 years
- Bachelor of Science
- Engineering
- Profit sharing
- Health insurance

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QA / Documentation Specialist
Qualitech Management Solutions —Barceloneta, PR
Support quality assurance and documentation activities for pharmaceutical manufacturing operations. Identify opportunities to improve documentation processes…
$20 - $40 an hour
Quick Apply
12d
Regulatory QA Specialist
HR Works —Barceloneta, PR
Strong understanding of GMP documentation and Quality Systems. Experience reviewing and approving documentation within the pharmaceutical or other regulated…
$30 - $45 an hour
Quick Apply

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Quality Assurance Specialist

Kelly Services -
Barceloneta, PR

Quick Apply

Job Details

Full-time

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Vision insurance
Retirement plan
Paid sick time

Qualifications

Statistical Process Control
GMP
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Regulatory/legal compliance standards in production
Laboratory information systems (LIS)
Manufacturing
Document management systems
Legal compliance
Research & development
Pharmaceutical manufacturing facility experience

Full Job Description

At Kelly® Science, Engineering, Technology & Telecom (SETT), we’re passionate about helping you find a job that works for you. How about this one?
We’re seeking an Quality Assurance Specialist to work with one of our top global biopharmaceutical clients in the Barceloneta PR area. With us, it’s all about finding the job that’s just right
Purpose:
The Quality Associate supports the Global Biologics Quality Function within Operations. Expectations that the Quality Associate III will maintain high-quality levels on all aspects of their job, while achieving high levels of efficiency.
Responsibilities:
• Responsible for various aspects of the product’s quality assurance related to their functional area.
• Ensures that product is consistently manufactured in conformance with Customer’s Quality System requirements and all applicable regulatory requirements throughout the network, including third party manufacturers.
• Support troubleshooting and resolution of quality compliance issues.
• Communicates with management for Quality Initiatives, Projects, Product Transfers, etc.
• Incumbent is responsible for ensuring compliance with Customer’s Quality Systems and cGMPs.
Qualifications
•Bachelor’s Degree required in Science or Engineering
•3+ years of combined experience in Manufacturing, QA, R&D in pharmaceutical, biologics, device or chemical industry
•Must be familiar with use of statistical quality systems, electronic document management and laboratory information management.
•Must also be familiar with Customer Quality Systems as well as cGMP and other regulatory requirements.
•Strong communication Skills, both oral and written.

Hybrid Onsite Schedule Tues, Wed, Thurs on site

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. 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.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

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.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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Refine Your Search

regulatory qa jobs in manatí pr

Quality Assurance Specialist

QA / Documentation Specialist

Regulatory QA Specialist

Quality Assurance (QA) Specialist II

QA Specialist

Senior IT Operations Support Specialist

Computer System Validation (CSV) Specialist (EBR System)

Validation Engineer

Project Manager - MES

Senior Quality Analyst

Senior Project Manager - (PE License) - Construction

Project Manager - Air Quality

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