Onsite GMP QA Associate II - Quality & Compliance
Duke PF
Duke University is seeking a GMP, Quality Assurance Associate II to ensure products, materials, and processes in Duke’s GMP programs meet the highest quality and compliance standards. You will support the MC3 GMP Facility, partnering across manufacturing, engineering, validation, and quality to drive quality systems and inspections. You will help shape continuous improvement, maintain quality metrics, and participate in multiple development programs, with on-site work and a competitive pay range #J-18808-Ljbffr Duke PF
$86.71k - $140.13k
...Regulatory Affairs & Quality (ORAQ) is looking for a GMP, Quality Assurance Associate II, to join our team. In... ...standards of quality and compliance. You will play a key... ...Experience serving as final QA signature for release... .... This position is Onsite. The work is performed...SuggestedWork experience placementWork at officeShift work- Duke University is seeking a GMP Quality Assurance Associate II to join the Marcus Center for Cellular Cures (MC3). The role supports QA activities ensuring products, materials, and... ...processes meet high standards of quality and compliance. You will work with manufacturing,...Suggested
$85.1k - $106.4k
...for the position of Quality Assurance Specialist II reporting to the Senior... ...2-3 shift to support GMP operations on... ...aseptic techniques and compliance standards. A successful... .... Quality Assurance (QA) Specialist II will be... ...: Employees based onsite may need to travel...SuggestedFull timeWorldwideFlexible hoursShift work- Novartis is seeking a Manufacturing Quality Assurance Specialist in Durham, NC for an onsite role. You will partner with manufacturing teams to ensure products meet GMP, CFR, FDA, and EU requirements, from shop floor to release. The position emphasizes deviations, investigations...Suggested
- ...Quality Assurance Specialist II Location: RTP NC, 27709 Duration: 6 Months This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical... ...This role will assure corporate compliance with applicable GCP, GLP, GCLP...SuggestedFlexible hours
$89.6k - $166.4k
...Description Summary #LI-Onsite Location:... ...The QC Specialist II is a highly skilled... ...Novartis' Small Molecules Quality Control laboratory... ...within a GMP-regulated environment... ...stability samples in compliance with GLP and cGMP requirements... ...across QA, QC, MS&T, Engineering...Work experience placement- JOB SUMMARY The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting... ...areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA... ...feedback as needed MQA Specialist II Associate degree / Bachelor’s degree strongly preferred...Contract workImmediate startNight shiftRotating shift
$43.08 - $80 per hour
Summary Quality is not just a checkpoint here—it is the... ...highest standards of quality, compliance, and scientific rigor. From shop... ...Durham, NC and will be an onsite role. Novartis is unable to... ...compliant processes aligned with GMP requirements. Support media...Hourly payRelocation packageMonday to FridayShift workDay shift- ...position is responsible for the compliance review of Biopharmaceutical Development GMP data. This includes the review and... ...laboratory investigations and deviations associated with the biopharmaceutical... ...or equivalent. Experience in QA review of analytical data (release...
- ...consulting firm is looking for a QA Consultant in Morrisville, NC.... ...candidate will provide quality oversight of GMP systems, manage investigations and ensure compliance with regulations. Candidates should... ...is available for this onsite position. #J-18808-Ljbffr Verista
- ...seeking an MQA Specialist to support manufacturing operations on the GMP floor, ensuring real-time guidance and audit readiness. The role... ..., SOP reviews, and routine facility assessments to maintain quality and regulatory readiness on a fast-paced production line. #J-18...
$28 - $31 per hour
...s note: This is a supportive QA role focused on Review and approval... ...would be amazing. RTP Onsite Duration: 6 Months The Quality Assurance Associate II (Contractor) is responsible for... ...not limited to a review of GMP raw data for compliance. The QA Associate II will perform...Contract workFor contractorsRemote workNight shift$27 - $29.85 per hour
...Quality Assurance Associate II Location: RTP NC Duration: 06 Months Pay rate: $27.00/hr - $29.85/hr The Quality Assurance Associate... ...include but are not limited to a review of GMP raw data for compliance. The QA Associate II will perform all duties in a manner consistent...For contractors$138.6k - $257.4k
...Description Summary Join Novartis as our QA Operations Head and play a... ...ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an... ...Making, Leadership #LI-Onsite #J-18808-Ljbffr Novartis Group...- ...healthcare recruitment firm is seeking a QC Associate I/II to support key operational aspects of... ...performing testing and adhering to GMP requirements, alongside responsibilities... ...have a relevant degree and experience in quality systems. You'll engage in method development...
- ...University’s Marcus Center for Cellular Cures seeks a QA Regulatory and Compliance Associate for our on-site GMP manufacturing lab in Durham, NC. You will ensure... ..., support inspections, and educate staff on quality plans while driving continuous process improvements...
- ...About the job Quality Assurance Specialist Quality Assurance... ...VEEVA is preferred. M-F, onsite Quality Assurance... ...duties: Provide Quality and Compliance oversight for manufacturing of... ...finalized Master Specifications and associated release documentation in the...Work experience placementFlexible hours
- ...transforming lives. Role Objectives The Senior Quality Assurance (QA) Associate plays a critical role within the... ...activities are conducted in compliance with applicable regulatory standards... ...Strong communicator Adaptable Ensure GMP and GDP compliance across all regulated...Temporary workWork at officeFlexible hours
- The Specialist, Quality Assurance Raw Materials (QARM) is responsible... ...quality assurance activities associated with the sampling, review,... ...the timely availability and compliance of materials used in biopharmaceutical... ...Systems Support Provide QA support and oversight for...
- ...Quality Specialist III The Quality Specialist III is responsible... ...Specialist III will work closely with QA leadership, operating with... ...to maintaining regulatory compliance, inspection readiness, and operational... ...of relevant experience in a GMP-regulated environment,...Contract workWork at officeLocal area
$138.6k - $257.4k
...Join Novartis as our QA Operations Head and play a pivotal... ...ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an opportunity... ...people click here. #LI-Onsite Why Novartis: Helping...- ...Direct Client Location: Research Triangle Park, NC Job Title: Quality Control Associate II Duration: 1 Year+ Primary Responsibilities The execution... ...proactively communicating with management regarding cGMP compliance and issues. Collaborating effectively within the team...
- Your Contribution The Loan Officer Certification & Quality Assurance Specialist serves as the primary subject matter expert responsible... ...and performance evaluations to ensure accuracy, consistency, compliance, and operational excellence throughout the lending function....Full timeWork at office
- ...Biopharma, Inc. in Durham, NC is seeking a Specialist, Quality Assurance Raw Materials (QARM) to ensure quality and regulatory compliance for raw materials used in clinical and commercial manufacturing. This role provides QA oversight in a cGMP environment and partners with...
- ...serious unmet medical needs. We work to restore quality of life to those with debilitating... ...throughout the manufacturing process. The QA Specialist will perform quality inspections... ...Follow current Good Manufacturing Practices (GMP) and company quality procedures Complete...Local areaShift work
- ...expectations into appropriate quality standards and provide... ...to ensure overall compliance with AstraZeneca and Regulatory... ...are met. Provide QA input into internal... ...documentation and labels for GMP manufacture/packaging,... .... Support activities associated with QA release of Drug...
- ...BioSciences, Inc in Durham, NC is seeking a Quality Specialist III to provide dedicated... ...performing deviation assessments, and ensuring compliance with regulatory standards. The ideal... ...sciences field, 5+ years of experience in a GMP environment, and strong attention to...
- Precision BioSciences, Inc. is seeking a Quality Specialist III responsible for providing... ...deviation assessments, and supporting regulatory compliance. The ideal candidate will have a Bachelor... ...and over 5 years of experience in a GMP-regulated environment. Strong attention...Work at office
- ...experience, or Equivalent combination of education and regulatory, quality, compliance and/or industry experience. Skills and Abilities... ...software applications as needed to effectively conduct QA duties (e.g., Word, Outlook, Excel, SharePoint) Ability to...Contract workTemporary workFor subcontractorWork at office
$59.95k - $99.9k
6038 - QA Consultant / Quality Specialist Join to apply for the 6038 - QA Consultant... ...quality oversight of GMP systems, supports QC investigations... ...ensures the site maintains compliance with regulatory and... ...other QMS tools (preferred) Onsite requirement in Morrisville,...Temporary workWork experience placement
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