- DivIHN Integration Inc (Green Oaks, IL)
- …nutritionals). Regulatory area is preferred but may consider quality assurance , research and development/support, scientific affairs, operations, or ... our Talent Specialists Meghna at ### Rashi at ### Title: Regulatory Affairs Specialist Location: Abbott Park, IL Duration: 7 Months Description Responsible for… more
- DivIHN Integration Inc (Columbus, OH)
- …of us to learn more For further information please contact our Talent Specialist : Rashi | 630 8471027 Title: Medical Safety Reviewer Location: Columbus, OH Duration: ... Report Forms (CRFs) including query resolution and addenda writing, QA of data listings. May manage the activities of...adverse events and works with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …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 ... and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch...with specifications and procedures Works closely with Manufacturing and Quality Control to resolve open issues resulting from record… 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...with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused… more
- Aequor (Seattle, WA)
- …communication Experience working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP ... agencies strongly preferred. Strong knowledge of cGMPs and domestic regulatory requirements. Knowledge of manufacturing quality (manufacturing, packaging,… 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 ... and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch... regulatory agency preferred As applicable, experience with Quality Assurance oversight and support for all… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- The QA Specialist II - Engineering/Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other ... regulatory requirements are adhered to as it relates to...with the Engineering and Validation departments. Job Responsibilities Perform Quality review/approval of URS, FAT, SAT, IQ,OQ,PQ protocols and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview ... The QA Warehouse Incoming/Raw Material Specialist is an...quality and operations counterparts that include Manufacturing Operations, Quality Assurance , Engineering and Validation, Quality… more
- Medline Industries LP (Northfield, IL)
- … science, or related. Work Experience 2 years of experience in medical device regulatory affairs or quality assurance . Knowledge / Skills / Abilities ... Understanding of the current Regulatory environment and demonstrating the ability to perform within. Applied knowledge of FDA regulations and guidelines. Ability to… more
- Merck & Co. (Durham, NC)
- Job DescriptionDurham's Technical Services Specialist will be an energetic, technical leader with strong interpersonal, communication, and collaboration skills to ... Operations IPTs. Responsibilities may include but are not limited to: Author Quality Notifications of varying complexity within established timelines to ensure … more
- BioAgilytix (Durham, NC)
- …workflows. You are the bridge between the lab and the quality assurance team, combining observations on regulatory requirements with your knowledge of ... be a critical part of our beginning-to-end client data quality processes. Through your technical reviews of raw and...and more.We are looking for candidates who have practical regulatory experience with bioanalytical data in a corporate GxP… 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, ... create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and...and track result data; Report any deviations to the Quality Systems and Regulatory Manager in complete,… more
- 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
- Mindlance (North Wales, PA)
- Job Title: Senior Specialist Quality Assurance Job Location: North Wales, PA Zip Code: 19454 Top 3/5 Skills: 1) Product Inspection/Investigation 2) Complaint ... functional testing, and documents all findings in the complaint records. Senior Specialist Quality Assurance - Pharmaceutical Qualifications-- . Looking… more
- Integrated Resources, Inc (Spring House, PA)
- Job Title: Senior Specialist Quality Assurance - Level II (Associate) Job Location: Spring House, PA Duration: 6 Months Pay range: $28 - $32/Hour. on W2 ... documents all findings in the complaint records. Qualifications: . Looking for a Quality Assurance /Complaint Handling Unit Specialist for a 6-month contract.… 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... regulatory and industry expectations. . Assist the QA department in maintaining the Quality focused… more
- Nesco Resource (Central Islip, NY)
- …is partnering with an international Pharmaceutical manufacturer in their search for a Vendor QA specialist . This role would be based out of their Central Islip ... around the US and Canada. If you are a QA specialist who is looking to expand...years of relevant experience in a pharmaceutical-regulated industry in Quality Assurance and Compliance. 2+ years' experience… 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...with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused… more
- Sunrise Systems Inc (Seattle, WA)
- …communication Experience working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP ... agencies strongly preferred. Strong knowledge of cGMPs and domestic regulatory requirements. Knowledge of manufacturing quality (manufacturing, packaging,… more
- FUJIFILM Holdings America Corporation (Holly Springs, NC)
- …1 works closely with Quality Control, Analytical Development, Manufacturing and Quality Assurance to ensure compliance with GMP requirements. What You'll ... External US About This Role The QC LIMS Sr. Specialist 1 is accountable for support of the Laboratory...LIMS training, technical support, problem reporting and resolution(s) to Quality Control laboratory, QA , AD and Manufacturing… more
