GMP Quality Assurance Specialist II
Duke Clinical Research Institute
Duke Clinical Research Institute is seeking a GMP, Quality Assurance Associate II to ensure compliance and quality in GMP programs. You will support the Marcus Center for Cellular Cures and play an important role in clinical research and patient-focused manufacturing. Ideal candidates should have at least 5 years in a GMP environment, experience in training, and strong attention to detail. This role offers competitive pay and comprehensive benefits, as well as growth opportunities within a top medical school environment. #J-18808-Ljbffr Duke Clinical Research Institute
$86.71k - $140.13k
...System comprise Duke Health, a world‑class academic medical center. The Office of Regulatory Affairs & Quality (ORAQ) is looking for a GMP, Quality Assurance Associate II to join our team. In this role, you will help ensure that the products, materials, and processes used...SuggestedWork at officeShift work$55k - $86.9k
KBI Biopharma in Durham, NC, is looking for a Manufacturing Quality Assurance Specialist, responsible for supporting the Manufacturing process in a dynamic GMP environment. The role requires real-time guidance to Manufacturing teams, ensuring compliance with standards....Suggested$86.71k - $140.13k
...Hospice, Duke Health and Wellness, and multiple affiliations. Be You. The Office of Regulatory Affairs & Quality (ORAQ) is seeking a GMP, Quality Control Associate II to join our team. In this role, you will support the development, qualification, and execution of...SuggestedWork experience placementWork at office- KBI Biopharma is looking for a QA Manufacturing Specialist responsible for ensuring product quality and compliance with regulations and internal procedures. This... ...activities and requires experience in a GMP regulated environment. Candidates should possess a scientific...SuggestedNight shift
- ...Quality Assurance Specialist II This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical studies. Examples of activities within the scope of oversight and auditing include but are not limited to: preclinical...SuggestedFlexible hours
- ...SummaryThe QA Manufacturing Specialist is responsible for... ...and systems conform to quality standards, internal procedures... ...responsible for GMP activities to resolve deviations... ...Specialist II: BS/BA in scientific field... ...authority to make any assurance to the contrary.I attest...Work at officeImmediate startShift 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 II (Contractor... .... Activities include but are not limited to a review of GMP raw data for compliance. The QA Associate II will perform...For contractors$28 - $31 per hour
...amazing. RTP Onsite Duration: 6 Months The Quality Assurance Associate II (Contractor) is responsible for... ...include but are not limited to a review of GMP raw data for compliance. The QA... ...notified about new Quality Assurance Specialist jobs in Durham, NC . REMOTE - Quality...Contract workFor contractorsRemote workNight shift- Job Summary This position is responsible for the compliance review of biopharmaceuticals development GMP data. This includes the review and approval of release, in‑process, and stability test data. This position is also responsible for the review and approval of method...
- KBI Biopharma in Durham, NC is seeking a Principal QA Specialist responsible for compliance review of Biopharmaceutical GMP data. This role includes reviewing test data, supporting client audits, and providing QA oversight of laboratory activities. The ideal candidate will...
- ...recruitment firm is seeking a QC Associate I/II to support key operational aspects of... ...involves performing testing and adhering to GMP requirements, alongside responsibilities for... ...have a relevant degree and experience in quality systems. You'll engage in method...
- ...Senior Specialist, Quality Assurance The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio’s Vendor Qualification Program for GCLP, GLP, GCP and GMP vendors. The role performs vendor assessments and audits, ensures compliance with...Local area
- ...standards and expectations into appropriate quality standards and provide mentorship to... ...issuance of batch documentation and labels for GMP manufacture/packaging, support of on-the-... ...Demonstrated knowledge of Quality Assurance activities, ICH regulations, and FDA/EU GxP...
- KBI Biopharma, Inc. is seeking a Manufacturing Quality Assurance (MQA) Specialist to support GMP manufacturing operations. This role involves providing real-time guidance, leading compliance reviews, and collaborating with cross-functional teams to meet regulatory requirements...Shift work
- Beam Therapeutics is looking for a Sr. Specialist I in NC Product Quality Assurance to oversee laboratory and manufacturing operations at their facility in Durham, North Carolina. The ideal candidate will have a Bachelors or advanced degree, alongside over 10 years of...Flexible hours
- BioSpace in Durham, NC seeks a Quality Assurance professional responsible for ensuring compliance with regulations and quality processes. Key functions include reviewing batch production records and supporting audits. The role requires at least two years of QA experience...
- Precision BioSciences, Inc. is seeking a Quality Specialist III responsible for providing quality assurance support for Chemistry, Manufacturing, and Controls (CMC)... ...sciences discipline and over 5 years of experience in a GMP-regulated environment. Strong attention to detail...Work at office
- ...maintaining complaint files, responding to customers, and producing quality reports. Provide mentorship and education regarding customer... ...complaint handling, medical device reporting, FDA regulations, GMP, quality systems, and applicable clinical or laboratory functions...
- Job Description Client: Direct Client Location: Research Triangle Park, NC Job Title: Quality Control Associate II Duration: 1 Year+ Primary Responsibilities The execution of QC routine testing to include TOC, conductivity, and nitrates. Executing TOC method validations...
- ...Responsible for providing Quality Assurance support to Manufacturing Process Operations. Performs document review and approval of Master Batch Records, SOP's and Technical Documents. Collaborate directly with MS&T and manufacturing to support BOM review and approvals to...
- ...Summary This position monitors the overall Quality System status of the distribution center.... ...respective job functions, including GMP. Writes and revises Standard Operating Procedures... ...industry experience - Preferred Quality Assurance experience - Preferred Bachelor’s Degree...Permanent employmentLocal area
- ...Sr. Quality Assurance Specialist Location US-NC-Morrisville ID 2026-2070 Category Quality Assurance Position... ...mentoring to Operations personnel in achieving a high level of GMP compliance and instilling quality culture. On-Site...Full timeWork experience placementMonday to FridayDay shift
- Alcami Corporation in Morrisville is seeking a Senior Quality Assurance Specialist. This role is responsible for ensuring quality and compliance with... ...'s degree in Chemistry or related field, ten years of GMP experience, and proven ability in aseptic manufacturing. This...Full timeAfternoon shift
- ...responsible for ensuring compliance with internal quality documents, regulatory requirements, and cGMP.... ...thorough knowledge of Quality Systems, Quality Assurance and Quality Control including solid knowledge of global GMP Quality and Regulatory requirements.* Minimum of...Immediate startFlexible hours
- Senior QA Specialist Deviations and CAPAs page is loaded## Senior QA... ...Deviations and CAPAs in support of GMP manufacturing operations.... ...equivalent. Experience with Quality Systems to include Batch Record... ...the authority to make any assurance to the contrary.**I attest with...Immediate start
$113k - $156k
...review of Biopharmaceutical GMP data. This includes the review... ...deviations. The Principal QA Specialist provides exemplary service to... ...goals. Cultivates and maintains Quality culture. May perform as a... ...release, and stability samples. Assures activities comply with...Immediate start- A leading biotech company in Morrisville, North Carolina, is looking for a Quality Assurance Specialist to oversee manufacturing quality and compliance for commercial and investigational products. The role requires 3 years of experience in the biotech or pharmaceutical...Full timeMonday to Friday
- Precision BioSciences, Inc in Durham, NC is seeking a Quality Specialist III to provide dedicated quality assurance support for Chemistry, Manufacturing, and Controls... ...life sciences field, 5+ years of experience in a GMP environment, and strong attention to detail. The position...
- ...Job Description Job Description Job Title: Quality Assurance Specialist II Duration: 06 months with possible extension Office: Research Triangle Park, NC 27709 Pay rate: $34/hr. on W2 Job Description: ~ This position is responsible for providing QA oversight...Work experience placementWork at officeFlexible hours
- ...North Carolina is seeking a qualified candidate for a position responsible for the compliance review of biopharmaceutical development GMP data. This includes overseeing release, in-process, and stability test data, method qualifications, and laboratory investigations....
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