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Gmp Quality Analyst Jobs (NOW HIRING)

Kelly Services

Quality Analyst

Barceloneta, PR

How about this one? We're seeking an Quality Analyst to work with one of our top global ... Knowledge of GMP, safety regulations. Quality/compliance management skills. Fast paced and ...

Kellton Tech

QC Analyst III

Portsmouth, NH · On-site

$33/hr

GMP QC lab experience required. * Strong communication and problem-solving skills. * Experience with TrackWise, LIMS, and Microsoft Office Suite a plus.

Flora Food Group

Support site Food Safety programs and maintain a working knowledge of HACCP and GMP requirements. * Assist with quality investigations, root cause analysis, and corrective and preventive actions ...

Ampcus Inc

Quality Analyst

Hopewell Township, NJ · On-site

$39.12/hr

Title: Quality Analyst Duration: 09/21/2026 to 01/29/2027 (Possibility of Extension) Location ... GMP / GDP; • Up-to-date knowledge of DEA regulations • Experience working in the quality ...

Cynet Systems

Quality Analyst

Ewing Township, NJ · On-site

$34.40 - $39.40/hr

Quality Analyst Job Location: Titusville, NJ Job Type: Contract Job Overview: Pay Range: $34.40hr ... Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP. * Up-to-date knowledge ...

Flora Food Group

Food Quality Analyst

Olathe, KS · On-site

Support site Food Safety programs and maintain a working knowledge of HACCP and GMP requirements. * Assist with quality investigations, root cause analysis, and corrective and preventive actions ...

Pharmavise

GMP Professionals

Maple Grove, MN · On-site

Experience with GMP quality systems, including document management, change control, deviations, and CAPA. * Strong analytical and problem-solving skills, with the ability to interpret and apply ...

Dyne Therapeutics

Director, QA GMP Operations

Waltham, MA · On-site

$188K - $230K/yr

The Director of QA GMP Operations is responsible for management of GMP quality within our external ... Review batch records, analytical method reports and technical reports including regulatory sections ...

Dyne Tx

Director, QA GMP Operations (Waltham)

Waltham, MA · On-site

$188K - $230K/yr

Review batch records, analytical method reports and technical reports including regulatory sections ... Manage CDMO performance within Quality Agreement expectations and GMP compliance. * Drive ...

CYNET SYSTEMS

Quality Analyst

Titusville, NJ · On-site

$34 - $39/hr

Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP. * Up-to-date knowledge ... Conduct routine data analysis for Suspicious Order Monitoring. * Process day-to-day product quality ...

CYNET SYSTEMS

Quality Analyst

Titusville, NJ · On-site

$34 - $39/hr

Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP. * Up-to-date knowledge ... Conduct routine data analysis for Suspicious Order Monitoring. * Process day-to-day product quality ...

AllSTEM Connections

Quality Control Analyst I

Camarillo, CA · On-site

$82K - $86K/yr

... GMP procedures accurately • Ability to work independently and manage routine laboratory tasks ... QC laboratory or pharmaceutical industry experience preferred) • Previous experience in a fast ...

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How much do gmp quality analyst jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for gmp quality analyst in the United States is $32.41, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $37.02 per hour, depending on experience, location, and employer.

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Quality Analyst

Barceloneta, PR

Kelly Services
See more jobs at Kelly Servicesexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 17 days ago

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 Analyst 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 :
Responsible for implementing and maintaining the effectiveness of the Quality System. Support manufacturing operations in the resolution of events, impact assessment and documentation discrepancies.
Provide guidance for product/process impact analysis, perform holistic evaluation of events, review and approve investigations and risk-based evaluations in support to routine operations and product disposition.
Responsibilities :.
Support routine operations to ensure that all quality goals are met, and all practices and procedures comply with Customer policies and applicable regulations for the Quality areas under responsibility. Serve as backup for the QA Manager leading the team and providing support to quality initiatives.
Ensures investigations of plant events are evaluated in a timely manner; completed thoroughly and documented accurately in the plant CAPA system.
Performs product impact analyses for plant events and places product on QA hold where appropriate.
Participates on the Validation Review Board as the Manufacturing Quality Assurance function. Approves standard operating procedures; change management and risk management documents. Ensures all documents are in compliance with Customer global procedures and regulatory requirements.
Approves calibration requests, calibration out of tolerance and preventive maintenance records. Ensures that these documents have appropriate justifications according to product /process limits established.
•Demonstrates accountability and responsibility of EHS performance and compliance.
Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.
Oversees manufacturing operations to ensure practices are in alignment with approved procedures.
Provide support to the Compliance team during internal and external audits as required.
Provide guidance for new product introduction activities. Develop risk assessments to support manufacturing activities for new products and ensure material control until regulatory approval.
Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any
other program applicable according to the position duties.
Qualifications
Bachelor’s degree in biotechnology, Biology, Chemistry or Engineering. Masters Degree in Science preferred.
Four (4) years of experience in Pharmaceutical/Biotechnology industry in a similar position.
This position requires knowledge of quality / compliance /Investigations /Risk management as well as regulations and standards affecting biological products.
Excellent written and spoken communication skills in English and Spanish.
Knowledge of GMP, safety regulations.
Quality/compliance management skills.
Fast paced and adaptable to continuously changing environment. Subject to work with multiple priorities and interruptions and under reasonable pressure due to the nature and function of the area.
Assures the quality of manufactured products and processes per standard operating processes (SOP'S) and GMP (Good Manufacturing Practices). BS degree or 3-5 years equivalent experience. Daily Work Schedule Expectations ALL candidates must be available for any shift/weekend/holidays.
Associate Rotating shift – 4 days at 10hours
2 months rotation on each shift 1st, 2nd, 3rd shift
Area worked based in manufacturing schedule of 24/7 Is overtime offered or required?
  Must be available to work OT based in business needs
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® 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.
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