- Novo Nordisk Inc. (West Lebanon, IN)
- …Performs walk-through audits of NNUSBPI Manufacturing facilities Releases product based on Quality Assurance record review and approval by Manager, Quality ... experience in a pharmaceutical or biotechnology company with one (1) year direct Quality Assurance experience Knowledge, Skills, and Abilities: Ability to work… more
- Aequor (Thousand Oaks, CA)
- …equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or ... Fully remoteResponsibilities: Coordinate Global Incoming Quality Process Operations to support Global Process Owner lead. Interface with IQA Network, various… more
- Aequor (West Greenwich, RI)
- …Systems comply with cGMP practices and other applicable regulations Provide support for Global Process Owners executing key quality systems processes Ensures the ... 8-5 PM What is the working environment for this role? Role supports quality management systems, office based, EW will be supporting recall regulatory reporting 50%… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …records. Will be a QA presence on the manufacturing floor. Relationships Quality Assurance . Essential Functions Reviews all manufacturing and support records ... are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product...compliance with specifications and procedures Releases product based on Quality Assurance record review and approval by… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …is preferable that the candidate have 2 years + of experience working in Quality Assurance . Previous cell therapy experience is a plusKnowledge of cGMP ... Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one...in the treatment of multiple myeloma.Legend Biotech is seeking Quality Project Management Specialist as part of… more
- Merck & Co. (Durham, NC)
- Job DescriptionResponsibilities: Responsible for the quality aspects of good manufacturing practices (GMP) computerized systems and the supporting infrastructure ... company policies, procedures, and regulatory expectations. Be involved in all quality -related activities for computerized systems which are required by the company… more
- Aequor (Swiftwater, MN)
- …with 2&plus years Regulatory Affairs experience OR Master's degree in Regulatory Affairs/ Quality Assurance or an appropriate combination of other relevant ... Overview of the Position The Regulatory CMC Specialist will work closely with the Regulatory Site...Health Authority is helpful but not essential Knowledge of global regulations/guidelines, key Health Authority/Industry Guidance and trends are… more
- Merck & Co. (Rahway, NJ)
- …junior analysts in core cyber threat intel tradecraft, analysis, and productionResponsible for Quality Assurance and Quality Control (QA/QC) of CTI ... solutions that reduce risk and enable new organizational capabilities.The CTI Senior Specialist is responsible for the daily prioritization and actioning of Cyber… more
- Merck & Co. (Durham, NC)
- …specifically in pharmaceutical operations, technical operations, validation and/or process Quality Assurance . - Required Experience and Skills: Previous ... Job DescriptionSenior Specialist , Quality Systems and Compliance (P3)...Systems and Compliance (P3) Our company is expanding its global recombinant vaccine production network by investing and adding… more
- Merck & Co. (North Wales, PA)
- …who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) organizations within our Research & Development Division . ... Job Description Position Description: Senior Specialist , Financial Planning & Analysis Our company's mission...and analytical support to our Research & Development Division, Global Regulatory Affairs & Clinical Safety (GRACS), and QA… more
