- Spectraforce Technologies Inc (Bothell, WA)
- Title: Quality Assurance Specialist (Pharma ONLY - NON IT JOB) Duration: 06 Months Location: Bothell, WA *Schedule- 9:00pm - 7:30am, Sun - Wed** **Top ... skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …compliance with specifications and procedures Releases product based on Quality Assurance record review and approval by QA Manager Performs regular internal ... GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch...leading international regulatory agency preferred As applicable, experience with Quality Assurance oversight and support for all… more
- Aequor (Bothell, WA)
- …skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role ... a regulated cGMP environment. The primary focus of the QA Specialist role will be to support...consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test ... our next generation of cutting-edge medications. We are looking for multiple levels QA Specialists (I-IV) What we offer you: Leading pay and annual performance bonus… more
- Integrated Resources, Inc (Bothell, WA)
- …skills include- strong cross-functional experience, strong interpersonal skills Job Description: . The Quality Assurance Specialist position plays a key role ... regulated cGMP environment. . The primary focus of the QA Specialist role will be to support...compliance with regulatory and industry expectations. . Assist the QA department in maintaining the Quality focused… more
- Sunrise System inc (Bothell, WA)
- …skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role ... a regulated cGMP environment. The primary focus of the QA Specialist role will be to support...consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused… more
- Merck & Co. (Rahway, NJ)
- …with internal stakeholders and partners such as Chemical Engineering, Process Chemistry, Quality Assurance and pilot plant support staff.Support internal and ... Research and Development group has an opening for a Specialist based in Rahway, NJ. Join us and experience...for timely results.Support the execution of Good Manufacturing Practices ( GMP ) activities such solvent and excipient release for use… more
- Piper Companies (Spring Lake, MI)
- …computer system and implement changes. Work collaboratively with internal teams, specifically QA ( quality assurance ) in development and implementation of ... , good manufacturing practice, cGMP, current good manufacturing practice, vendor validations, Quality assurance , QA , GAMP, validation, validation plan,… more
- Catalent (Manassas, VA)
- …work with complex formulations to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for ... standards. Communicate any deviations to management. Assist the Quality Assurance team with special projects as...(Standard Operating Procedures and Test Methods) and Knowledge of GMP and quality systems For business and… more
- Merck & Co. (Durham, NC)
- …experience, including a minimum of six (6) years of work experience in a GMP environment supporting a technical or quality role. Required Experience and Skills: ... Job DescriptionDurham's Technical Services Specialist will be an energetic, technical leader with...Responsibilities may include but are not limited to: Author Quality Notifications of varying complexity within established timelines to… more
- Catalent (Manassas, VA)
- … Quality System documentation. Communicate any deviations to management. Assist the Quality Assurance team with special projects as required. Comply with SQF, ... and follow documents (Standard Operating Procedures and Test Methods); Knowledge of GMP and Quality systems.Basic Microsoft Office (Excel, PowerPoint, and Word)… more
- BioAgilytix (Durham, NC)
- …settings, and workflows. You are the bridge between the lab and the quality assurance team, combining observations on regulatory requirements with your knowledge ... role and you will be a critical part of our beginning-to-end client data quality processes. Through your technical reviews of raw and processed data, you will ensure… more
- Integrated Resources, Inc (Smyrna, GA)
- Job Title: Quality Administrative Specialist Location: Smyrna, GA [Hybrid role- 2 days onsite, 3 days remote] Duration: 06 Months on W2 (Temp to hire) JOB ... The goal of this function is to support the Quality Management Systems in the US Affiliate, including but...of the affiliate in accordance with national and international GMP and legal requirements. . Ensure QA … more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill a Quality Assurance Specialist ( GMP Auditing) position. This position will support the GMP Auditing department by ... Prepares written audit documents and reports and ensures the quality and accuracy of all audit documentation. + Identifies...amount of relevant experience for each level: + Associate QA Specialist - 0-2+ years + … more
- Randstad US (Burlington, MA)
- quality assurance specialist - gmp . + burlington...include: + working in a smoke free environment Skills + QA /QC + QAQC + Quality Assurance ... large company in the biopharmaceutical industry, is seeking a Specialist /Senior Specialist to support Quality ...appropriate escalation. + Identify risks and communicate gaps for quality and GMP process/systems. + Reviews and… more
- Bausch Health (Petaluma, CA)
- …mission of improving peoples lives with our health care products. Join our team as a ** Quality Assurance Specialist , GMP ** at our _Petaluma site_ ! We're ... in analytical lab equipment operation. + Review and approve various GMP documents including batch records, specifications, test methods, and validation reports.… more
- United Therapeutics (Eden Prairie, MN)
- …kidney disease. How you'll contribute The Senior QA Specialist - GMP Manufacturing, is responsible for supporting quality operations during GMP ... clinical manufacturing of bioengineered organs at Miromatrix. The Senior QA Specialist collaborates with and provides support...Certificates of Conformance + SOPs: Author, revise and approve Quality -related SOPs in eDMS. Own Change Controls + … more
- United Therapeutics (Eden Prairie, MN)
- …therapies to help patients with liver and kidney disease. How you'll contribute The Quality Assurance Specialist II ensures that all intermediates and ... documentation including SOPs, Work Instructions (WIs), MBRs, Specifications and TMs + Quality Metrics: Support QA manufacturing metrics + SOPs: Author and… more
- Seattle Children's (Seattle, WA)
- …the Seattle Children's Therapeutics with development, implementation, and maintenance of quality assurance systems and activities. Perform internal audits, ... Minimum two (2) years academic, biotechnological, or pharmaceutical industry hands on QA experience in a GMP biologics manufacturing environment. Required… more
- Prime Matter Labs (Miami Gardens, FL)
- …review and for coordinating and/or executing various activities in support of validation and GMP Compliance. The QA / Compliance Specialist will be involved ... and every step in between. We're looking for a QA / Compliance Specialist who will be...operations to ensure that operations are in compliance with GMP and Company procedures. + Conduct investigations into failures… more
