QA Area Specialist I - SDF (2nd shift)
Novo Nordisk A/S
Benefits Leading pay and annual performance bonus for all positions All employees enjoy generous paid time off including 14 paid holidays Health Insurance, Dental Insurance, Vision Insurance – effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave Free access to Novo Nordisk-marketed pharmaceutical products Tuition Assistance Life & Disability Insurance Employee Referral Awards The Position Ensure Batch Production Records (BPRs) and/or relevant quality processes are compliant with regulations and/or relevant standard operating procedures (SOP's) and guidance. Accountable for Quality review & approval of Change Requests (CR's), Deviations & other documentation. Perform Self Audits (in conjunction with line of business (LoB)), Quality Assurance (QA) presence & process confirmation on shop floor. Relationships Reports to Manager, Quality Assurance. Essential Functions Ensure site compliance with Regulations, International Organization for Standardization (ISO) standards, corporate & local SOPs Review & approve documentation for Quality approval – batch records and other documentation Support, review & approve investigations & root-cause analysis using LEAN tools and continuous improvement Participate in process confirmations & Go Look Sees Evaluate trend & report data for Quality Management Reviews (QMRs) & Annual Product Review (APR) reports Perform QA role to review and approve local production related Customer Complaint Investigations (escalate if necessary) Participate in & support the audit management team as needed during internal, external audits and inspections Responsible for training of AP and FP members responsible for conducting investigations Follow all safety & environmental requirements in the performance of duties Other duties as assigned Physical Requirements May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required to be on your feet for up to a 12-hour shift. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections. Qualifications Associate’s degree in life sciences or related field from an accredited college required. Bachelor’s degree preferred May consider a High School Diploma or GED with a minimum of six (6) years of experience in QA or related quality experience Minimum of two (2) years QA and /or quality related, or API experience required, preferably in the pharmaceutical industry Quality Experience preferred General knowledge of pharmaceutical regulations & quality systems preferred Knowledge of Quality and one or more of the following: Aseptic Production, Business Support, QC, Production Support, Warehousing/Transport, API, and/or Finished Production processes preferred Basic computer skills in MS Office, MS Project, PowerPoint, etc. required We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at View phone number on click.appcast.io. This contact is for accommodation requests only and cannot be used to inquire about the status of applications. #J-18808-Ljbffr Novo Nordisk A/S
- ...treatments for patients with type 2 diabetes. SDF maintains a curious and pioneering spirit,... ...of business (LoB)), Quality Assurance (QA) presence & process confirmation on shop... ...required to be on your feet for up to a 12-hour shift. May require corrected vision to 20/20 or...Afternoon shiftLocal areaShift work
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- ...years experience or MS with 8+ years experience in a CGMP regulated environment within biopharmaceuticals or equivalent. Experience in QA review of analytical data (release, in‑process, and stability). Experience in reviewing method qualifications/validations and...Suggested
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...full lifecycle of GMP operations. Represent QA in cross‑functional settings and provide... ...and trend quality metrics to identify areas of concern. Assist with inspections and manage... ...fast‑paced environment. Adaptability to shift priorities. Problem‑solving skills and a...Work at officeShift work- 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...
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Job Summary The Manufacturing Quality Assurance (MQA) Specialist supports the manufacturing process within a rapidly expanding GMP contract... ...to represent quality and become qualified trainers. Salary & Shift Pattern Salary range: $55,000-$86,900. MQA Specialist shifts: 1...Contract workShift work- 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... ...interface with QA and functional area staff on vendor qualification topics. Identify...Local area
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...approval of in-process, release, and stability test data. Provides QA oversight of analytical and microbial laboratory activities... ...laboratory investigations and laboratory deviations. The Principal QA Specialist provides exemplary service to both internal and external...Immediate start$28 - $31 per hour
...Description: Manager’s note: This is a supportive QA role focused on Review and approval of... ...Get notified about new Quality Assurance Specialist jobs in Durham, NC . REMOTE - Quality... ...Assurance Senior Quality Assurance Area Specialist I - MSAT Focused We’re unlocking...Contract workFor contractorsRemote workNight shift- ...to combination products. Perform quality assurance activities, including inspections of production equipment (cleanliness, gowning, area line clearances), in-process packaging checks, AQL inspections, and floor audits. Review and disposition manufacturing/packaging and...
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...related field. Experience serving as final QA signature for release of raw materials or... ...fast‑paced environment. Adaptability to shift priorities. Problem‑solving skills and a... ...Track and trend quality metrics to identify areas of concern. Assist with inspections and...Work experience placementWork at officeShift work- NCBiotech is seeking a Quality Specialist III in Durham, NC, responsible for ensuring quality assurance support for Chemistry, Manufacturing... ...release review, deviation assessments, and collaborating with QA leadership. The ideal candidate will have a Bachelor's degree in...
- Precision BioSciences, Inc in Durham, NC is seeking a Quality Specialist III to provide dedicated quality assurance support for Chemistry, Manufacturing, and Controls operations. This role includes reviewing batch releases, performing deviation assessments, and ensuring...
- ...week across 10 southeastern and mid‑Atlantic states. Category / Area of Expertise Retail Operations Job Requisition 507792 Address USA... ...and seek to reduce costs and improve labor productivity Follow QA daily check list and sanitation standards set by Food Lion...Local areaNight shift
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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....- KBI Biopharma, Inc. is seeking an individual contributor for a Quality Assurance role focused on compliance with regulatory guidelines. This position involves interfacing with clients regarding batch status, managing quality issues, and ensuring systems are effective and...
- Novo Nordisk A/S in Durham, North Carolina seeks a Quality Assurance professional to ensure compliance with regulations and internal standards. The role involves documentation review, root cause analysis, and participation in audits. Candidates should have at least two ...
- 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 laboratory...
$113k - $156k
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...- ...QA Compliance Specialist Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely... ...classifications of DTRs. Collaborates with functional areas to improve the Deviation/CAPA system to include support in...
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- ...Raleigh, a Campus of Duke University Hospital Working hours: ~1st shift ~2nd shift ~3rd shift Occupational Summary Performs routine manual housekeeping work cleaning areas within a DUHS entity. Work Performed Empty trash. Clean, mop,...Afternoon shiftNight shiftDay shift
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- Cintas is seeking a Warehouse Associate - Loader/Unloader in Durham, NC. The incumbent will drive company trucks to designated areas for unloading soiled products and load clean uniforms and floor mats on trucks according to customer routes. Candidates must be authorized...Afternoon shift
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