- Cipla (Central Islip, NY)
- …schedule will be Monday to Friday Responsibilities/ Accountabilities Prepare and review Change Controls, Technical Deviations, Methods, Specifications, COAs, ... outside of Cipla's US Subsidiaries or Affiliates Job Title Packaging Technical Writer Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY… more
- Cipla (Central Islip, NY)
- …finished drug products. Responsibilities include but are not limited to GMP documentation review and supporting other QA functions as needed. In this role, the ... associate II" include but are not limited to the following: Review documentation for manufacturing activities associated with commercial, development, and… more
- Tradeweb (New York, NY)
- …+ Prepare quarterly impairment and fair value analyses, including drafting supporting technical accounting memos + Review valuations prepared by the corporate ... Tradeweb is opening an exciting new role for a Technical Accountant - Equity and Debt Securities, to oversee...US GAAP + Participate in investment due diligence, including review of financial information and legal agreements and … more
- Formation Bio (New York, NY)
- …deliverables and compliance with GMP and regulatory standards. Documentation: Author and review technical documents in collaboration with Quality colleagues to ... on the Formation Bio pipeline. This role requires a blend of technical expertise, strategic thinking, leadership capabilities, and a strong regulatory and industry… more
- Cipla (Hauppauge, NY)
- …plans. Collect and analyze all data, write final reports and obtain approvals. Review technical documentation such as batch records, SOPs, calibration records, ... senior management. Maintain departmental compliance pertaining to departmental SOPs, periodic review and reporting of the environmental monitoring system. Generate, … more
- Cipla (Central Islip, NY)
- …/ comparison reports and any other study reports. Prepare and review laboratory investigation (OOS/OOT/Deviation) reports and ensure compliance of same. Verifying ... edition, supplement, amendment, or other changes of any Pharmacopoeia are in effect. Review of laboratory audit trials during data review against standard… more
- Cipla (Hauppauge, NY)
- …standards for completeness of the labels against standard operating procedures (SOPs). Review of laboratory audit trials during data review against standard ... of necessary improvements in the identified areas. Actively participating in review of data related to laboratory investigations and incidents and ensuring… more
- Merck & Co. (Buffalo, NY)
- …at product workshops and conferences, as well as consistent and ongoing review of our Company's promotional materials.- Utilizing analytical skills and tools to ... Requirements:- - Valid Driver's license- Preferred Skills/Experience: - Ability to convey technical concepts accurately and clearly-- Prior experience working in a … more
- Cipla (Central Islip, NY)
- …tablets and capsules to include delivery, in-process samples in a defined schedule. Review and compile the documents generated during the production of tablets and ... quality, productivity, and performance expectations and execution of manufacturing operations. Review batch record after finishing each step for correctness. Provide… more
- Stony Brook University (Stony Brook, NY)
- …to Associate Technical Director SL-5, as assigned. + Conducts monthly review of product QC logs and instrument maintenance logs. Ensures all regulatory ... our team, who will demonstrate a high degree of technical competence and knowledge in current methods and techniques....and LIS (Clinisys & CoPath) order entry and result review screens, new tests additions to the test menu,… more
