Vruxxxxxx - Quality Assurance Associate Job Profile in Jersey City, NJ * Quality Assurance ... GLP practices, analytical techniques, documentation, and quality systems. I am detail-oriented ...
New
Vruxxxxxx - Quality Assurance Associate Job Profile in Jersey City, NJ * Quality Assurance ... GLP practices, analytical techniques, documentation, and quality systems. I am detail-oriented ...
New
Vruxxxxxx - Quality Assurance Associate Job Profile in Jersey City, NJ * Quality Assurance ... GLP practices, analytical techniques, documentation, and quality systems. I am detail-oriented ...
New
Durham, NC · On-site
$90 - $120/hr
The QA Auditor will ensure the accuracy, integrity, and compliance of toxicological research ... The successful candidate will be independent, accountable, and able to deliver polished, GLP ...
Durham, NC · On-site
$90 - $120/hr
The QA Auditor will ensure the accuracy, integrity, and compliance of toxicological research ... The successful candidate will be independent, accountable, and able to deliver polished, GLP ...
Exton, PA · On-site
Quality Assurance (QA) Specialist / Manager - DMPK Location: Exton, PA Department: DMPK (Drug ... Ensure compliance with GLP regulations, company SOPs, client requirements, and industry best ...
Quick apply
Exton, PA · On-site
Quality Assurance (QA) Specialist / Manager - DMPK Location: Exton, PA Department: DMPK (Drug ... Ensure compliance with GLP regulations, company SOPs, client requirements, and industry best ...
San Diego, CA · On-site
$120 - $160/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
San Diego, CA · On-site
$120 - $160/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
Everett, WA · On-site
$80K - $87K/yr
Audits all disciplines (examples of disciplines include Method Validations, Non- Clinical GLP ... Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test ...
Everett, WA · On-site
$80K - $87K/yr
Audits all disciplines (examples of disciplines include Method Validations, Non- Clinical GLP ... Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test ...
Chicago, IL · On-site
$100 - $170/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
Chicago, IL · On-site
$100 - $170/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
Raleigh, NC · On-site
$90 - $130/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
Raleigh, NC · On-site
$90 - $130/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
$100 - $170/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
$100 - $170/hr
At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing. * Must be able to travel to perform audits. * Demonstrated working knowledge of 21 CFR Part 58 ...
QUALITY ASSURANCE TECH 3rd Shift Openings in Shenandoah. LLOYD, Inc. has an immediate opening for a ... the GLP Regulations of the FDA and the Corporate Operating Procedures. Requirements include ...
Quick apply
QUALITY ASSURANCE TECH 3rd Shift Openings in Shenandoah. LLOYD, Inc. has an immediate opening for a ... the GLP Regulations of the FDA and the Corporate Operating Procedures. Requirements include ...
... GLP practices, analytical techniques, documentation, and quality systems. I am detail-oriented ... Quality Assurance My Qualifications and Preferences * Job Type: Non IT Job * Work Authorization:
New
... GLP practices, analytical techniques, documentation, and quality systems. I am detail-oriented ... Quality Assurance My Qualifications and Preferences * Job Type: Non IT Job * Work Authorization:
New
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
The Quality Assurance (QA) Assistant is an entry level trainee position. The QA Assistant will ... GLP) and non-GLP, to support clients from target identification through preclinical development.
The Quality Assurance (QA) Assistant is an entry level trainee position. The QA Assistant will ... GLP) and non-GLP, to support clients from target identification through preclinical development.
Knoxville, TN · On-site
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
Knoxville, TN · On-site
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
Pasadena, CA · On-site
$198 - $236/hr
GMP/GLP Supplier Quality Management * Responsible for the end-to-end supplier qualification ... Serve as the primary QA point of contact for Xencor's contracted QP service provider(s) and EU/UK ...
Pasadena, CA · On-site
$198 - $236/hr
GMP/GLP Supplier Quality Management * Responsible for the end-to-end supplier qualification ... Serve as the primary QA point of contact for Xencor's contracted QP service provider(s) and EU/UK ...
Pasadena, CA · On-site
GMP/GLP Supplier Quality Management * Responsible for the end-to-end supplier qualification ... Serve as the primary QA point of contact for Xencor's contracted QP service provider(s) and EU/UK ...
Pasadena, CA · On-site
GMP/GLP Supplier Quality Management * Responsible for the end-to-end supplier qualification ... Serve as the primary QA point of contact for Xencor's contracted QP service provider(s) and EU/UK ...
Canton, MA · On-site
$50 - $70/hr
Position Overview An entry level quality assurance position. Responsibilities include, but are not ... GLP records and archival activities; and assisting QAU Management with internal and external ...
New
Canton, MA · On-site
$50 - $70/hr
Position Overview An entry level quality assurance position. Responsibilities include, but are not ... GLP records and archival activities; and assisting QAU Management with internal and external ...
New
This Clinical Quality Assurance Senior Leader provides strategic leadership and operational ... Good Laboratory Practices (GLP), Good Clinical Practices (GCPs), and Good Pharmacovigilance ...
This Clinical Quality Assurance Senior Leader provides strategic leadership and operational ... Good Laboratory Practices (GLP), Good Clinical Practices (GCPs), and Good Pharmacovigilance ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Ensure all GMP, GLP, GCP operations are in compliance , Establish training and audit programs, as ... Be responsible for release or rejection of GMP materials and utilize QA staff to manage the ...
Ensure all GMP, GLP, GCP operations are in compliance , Establish training and audit programs, as ... Be responsible for release or rejection of GMP materials and utilize QA staff to manage the ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
The most popular types of Glp Qa jobs are:

Jersey City, NJ • On-site
Other
Posted 3 days ago
New
I recently completed my Master of Science in Pharmaceutical Sciences from Rowan University and hold a Bachelor of Pharmacy. Through my academic training and analytical chemistry internship, I gained hands‑on experience with GMP/GLP practices, analytical techniques, documentation, and quality systems. I am detail-oriented, eager to learn, and enjoy working in collaborative, fast‑paced environments where quality and patient safety are top priorities. I am looking for an opportunity to contribute to a growing organization while continuing to develop my skills in Quality Assurance and clinical research.
My Skill Set