- 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 (West Greenwich, RI)
- …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% ... who is comfortable working remotely and able to work independently, understanding quality management systems (QMS systems), looking for a candidate who has… 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...and approve multisite procedures, deviation, change control and other quality records to support RM Network. Candidate must have… 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 ... certify compliance with specifications and procedures Releases product based on Quality Assurance record review and approval by QA Manager Performs regular… more
- Merck & Co. (Rahway, NJ)
- …allows the organization to continue advancing medical innovation and improve lives. SPECIALIST (P-2), -Audit and Assurance ServicesOur Company Corporate Audit ... is to provide value-added independent and risk based audit and assurance services.Position Responsibilities:Under the direction of the Client Audit Director ("CAD")… 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 ... an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Quality Project Management Specialist as part of the Quality team based in… 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...industry experience eg, Quality and/or Manufacturing Requires knowledge and understanding of CMC… 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) Our company is expanding its global recombinant vaccine production network by investing and… 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
