Biotech QA Specialist - Onsite, GMP & Compliance
Globalchannelmanagement
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 industry, strong knowledge of FDA requirements, and the ability to manage multiple projects effectively. Familiarity with KNEAT, SAP, and VEEVA is preferred. This is a full-time, on-site position with a schedule from Monday to Friday. #J-18808-Ljbffr Globalchannelmanagement
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- ...North Carolina is seeking a Manufacturing Quality Assurance Specialist to ensure compliance with regulatory standards in cGMP operations. The role... ...manufacturing floor, documentation review, and supporting various QA-related tasks. The ideal candidate will have a Bachelor’s...
$86.71k - $140.13k
...Quality (ORAQ) is looking for a GMP, Quality Assurance Associate... ...highest standards of quality and compliance. You will play a key part in... ...of GMP operations. Represent QA in cross‑functional settings... ...reports. Location This position is onsite. Work is performed on‑site or...Work at officeShift work- Beam Therapeutics is seeking a Specialist II for NC Product Quality Assurance in Durham, NC... ...and manufacturing operations to ensure compliance with Good Manufacturing Practices. The Specialist... ...3-4 years of relevant experience in the biotech industry. A detail-oriented approach and...
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- ## QA Specialist II, Quality Operations (Combination Products)Applyremote... ...the first publicly-traded biotech or pharmaceutical company to... ...procedures at the RTP campus.* Review GMP documentation, including,... ...accuracy, completeness, and compliance with UT policies and...
- United Therapeutics Corporation is seeking a Senior QA Specialist, Quality Operations in RTP, North Carolina. In this on-site full-time role, you will ensure compliance with GMP through quality operation activities for clinical and commercial drugs. The ideal candidate...Full time
- Overview QA Specialist (Biotech) needs 3 years of experience in the biotech/pharmaceutical industry within research and development or commercial... ...release activities within the ERP system, ensuring compliance with applicable regulations and internal procedures. Get Certificates...
$55k - $86.9k
...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. The ideal candidate will have GMP...- KBI Biopharma in Durham, 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...
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KBI Biopharma Inc. in Durham, NC is seeking a Principal QA Specialist responsible for compliance review of Biopharmaceutical GMP data. You will provide QA oversight of various laboratory activities and ensure patient safety and regulatory compliance. The ideal candidate...$86.71k - $140.13k
...Regulatory Affairs & Quality (ORAQ) is seeking a GMP, Quality Control Associate II to join our... ...in a GMP cleanroom environment Onsite This position is Onsite. The work is performed... ...development and GMP activities in full compliance with regulatory and quality standards...Work 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 position provides... ...activities and requires experience in a GMP regulated environment. Candidates should possess...Night shift
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- Join Novo Nordisk in Durham, NC as a Quality Assurance professional, responsible for ensuring compliance with regulations and quality processes. This role involves reviewing documentation, supporting investigations, and conducting audits to maintain high-quality standards...
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$66.2k - $86.8k
## QA Specialist (Hybrid)Applylocations: North Carolina, Raleightime type... ...system activities to ensure compliance with cGMPs, internal procedures... ...assurance functions in a GMP setting (e.g., batch record review... ...(a minimum of 3 designated onsite days - T, W, TH)• Values...Work experience placementWork at office- Merck in Raleigh, NC is seeking a Quality Assurance professional to lead audits and ensure compliance with global regulatory requirements. This role involves conducting audits, analyzing data, and collaborating with teams to uphold quality standards. The ideal candidate...Remote job
- ...experience in a regulated manufacturing environment. The successful candidate will direct quality assurance activities, maintain compliance, and improve processes through effective corrective actions. Position offers competitive health insurance and career development...
- BioSpace is seeking a Quality Assurance professional in Durham, NC to ensure compliance with regulations and approve quality documentation. The ideal candidate will have at least two years of QA experience, preferably in the pharmaceutical industry, and excellent...
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