- Aequor (Waltham, MA)
- …Perform the following activities: Document Control: Run Daily Report - QualiPSO Veeva Documents Accept/Closed DCR's Assist with procedure assignment in curriculums ... (assist training coordinator) Assist with paper document archiving and indexing Assist with logbook/MMRs/BMRs management where needed - scanning, archiving, closing out request forms Attend meetings as needed. Assist with Document Vault Assist with general DC… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded Validation Specialist that can help drive our Strategic Operating Priorities.Invent - Pursue the Most ... They are a Competitive Advantage for UsSummary, Focus and PurposeThe Validation Specialist will be an energetic, technical contributor and leader with strong… more
- Aequor (Swiftwater, MN)
- …and other documentation that support site registrations, specific country documentation , and Annual reports. The Regulatory CMC Specialist prepares responses ... Overview of the Position The Regulatory CMC Specialist will work closely with the Regulatory Site...dossiers approved by Health Authorities Prepares and provides Regulatory documentation required for site registration and renewal activities CMC… more
- Merck & Co. (San Diego, CA)
- Job DescriptionTechnology Implementation Specialist will support our sales staff and customers as well as document and provide feedback to our engineering team. The ... Technology Implementation Specialist will also provide on-site, and remote troubleshooting, installation startups and training.Key responsibilities may include, but… more
- Aequor (Golden Valley, MN)
- DTB - PT, Flex Certifications and Specifications Specialist This is an ITQ Dynamic Talent Bench, 1300 hour track position. Seeking flexible, part-time talent with ... (please no Macs). JOB SUMMARY: The Certifications & Specifications Specialist will be responsible for supporting our team of...R&D, Sourcing, Labeling, etc.) to ensure all the right documentation and information is collected to comply with food… more
- Aequor (NV)
- …for you? 1) Warehouse operator, 2) transportation booking experience (ie prepared shipping documentation ), 3) short-term employment - it takes 3-4 months for us to ... Key Responsibilities o Transaction management Broker management Import for export Documentation records Country of origin Classifications Write, review, and update… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Are you ready to realize your potential? The Position The Senior Specialist , EEO Investigations role will work under the supervision of EEO Investigators ... addressing both internal and external complaints received by the Company. The Sr. Specialist will also be responsible for researching and analyzing data relevant to… more
- Aequor (Bothell, WA)
- …problem, and asset management PURPOSE AND SCOPE OF POSITION:The Benchtop Support specialist position will be responsible for providing IT support in our Digital ... guidance, GxP compliance, Software Development Life Cycle, and Good Documentation Practices.Comprehensive knowledge of SOPs, cGMPs, and other compliance requirements… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... assess Corrective and Preventive Actions Reviews and approves validation documentation Reviews and assesses deviations; includes tracking, follow-up and… more
- Merck & Co. (Durham, NC)
- …work. Provide the independent quality approval of key qualification/validation documentation such as policies, procedures, acceptance criteria, plans, protocols, ... and use of computerized systems. Provide Quality Unit review/approval of SDLC documentation . Mentor and provide guidance to junior members of the team. -… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewWe are actively seeking a proficient Master Data Governance Sr. Specialist with a specific focus on Materials orchestration throughout the End-to-End… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... OverviewThe Operations Support Specialist will be part of the Technical Operations team...BSL-2 cleanroom facility.Physical dexterity sufficient to use computers and documentation .Ability to accommodate shift work including evenings and weekends… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist I as part of the Technical Operations team based in Raritan, NJ. ... and 600, 601, and 610 is preferred. Experience authoring and executing documentation including but not limited to: Batch Records, SOPs, Work Instructions, CQV… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Inventory Control Specialist as part of the Technical Operations team based in Raritan, New ... Jersey. Role OverviewThe Operations Inventory Control Specialist will be part of the Raritan CAR-T Operations team responsible for building operations activity area… more
- Merck & Co. (Rahway, NJ)
- …working with trade compliance processes such as classification, licensing, documentation , and reporting; working with pricing procedures, condition types, and ... rebate processing within OtC module with focus on Gross to Net.; and experience in 3PL and WM integration.Up to 10% domestic and international travel required.Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... signature authority for deviation closure Reviews and approves Validation Documentation Reviews and assesses Corrective and Preventive Action Reports Participates… more
- Eclaro (Hamilton Square, NJ)
- Pharmacovigilance Specialist Job Number: 24-02811 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Pharmacovigilance ... Specialist for our client in Lawrenceville, NJ. ECLARO's client...and Excel Skills. Knowledge of Validation processes and associated documentation . Excellent verbal, writing, presentation, and project management skills.… more
- Eclaro (Alfred, ME)
- Plant Document Specialist Job Number: 24-02785 Use your skills where innovative technology solutions begin. ECLARO is looking for a Plant Document Specialist for ... a chance at this rewarding opportunity! Position Overview: The Plant Document Specialist is responsible for managing Document Control programs that ensure all… more
- Eclaro (Echo Lake, WA)
- Benchtop Support Specialist Job Number: 24-02953 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Benchtop Support ... Specialist for our client in Bothell, WA. ECLARO's client...guidance, GxP compliance, Software Development Life Cycle, and Good Documentation Practices. Comprehensive knowledge of SOPs, cGMPs and other… more
- Eclaro (Lynbrook, NY)
- Senior Desktop Support Specialist Job Number: 24-02952 Use your skills where innovative technology solutions begin. ECLARO is looking for a Senior Desktop Support ... Specialist for our client in Far Rockaway, NY. ECLARO's...in Active Directory administration, Windows operating systems, imaging technologies, documentation practices, and excellent communication skills. Pay Rate: 35.00-40.00$/Hour… more
