QA Area Specialist I - SDF (1st shift)
Novo Nordisk A/S
What we offer you: 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 14weeks 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 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. #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...Day shiftLocal areaShift work
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...Biopharmaceutical GMP data. This includes the review and approval of in-process, release, and stability test data. The Principal QA Specialist provides QA oversight of analytical and microbial laboratory activities, including but not limited to method qualification,...- LeadStack Inc. is seeking a Quality Assurance Specialist to ensure corporate compliance with GMP standards. Located in Research Triangle Park, NC, this role entails managing QA responsibilities and supporting product quality systems. The ideal candidate will hold a Bachelor...Contract work
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...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- ...critical documentation, and supporting the quality process on the shop floor. The ideal candidate will have a Bachelor's degree in life sciences and at least three years of relevant QA experience in a pharmaceutical environment. #J-18808-Ljbffr Initial Therapeutics, Inc.
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## KBI: US - Principal QA SpecialistApplylocations: USA - NC - Durham - Hamlin Rdtime type: Full timeposted on: Posted Yesterdayjob... ...laboratory investigations and laboratory deviations. The Principal QA Specialist provides exemplary service to both internal and external...Immediate start$55k - $86.9k
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- Overview Join to apply for the Sr QA Specialist role at BioSpace . The Senior Specialist, Quality Assurance Laboratory Operations leverages... ...Onboarding Training. Actively communicate with the various areas and departments to identify areas of improvement. Seek new ways...Full time
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Mercor is seeking a Remote Golf Video Annotation Reviewer to support a golf data annotation project. The role involves reviewing and correcting annotations on approximately 50 golf videos, each about 20 minutes long, focusing on quality control. The ideal candidate must...Remote jobHourly pay$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....- ...consulting firm located in North Carolina is looking for an experienced Quality Assurance professional. The role involves providing QA support to manufacturing processes, reviewing, and approving critical documentation. Candidates should have a Bachelor's degree and over...
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