- Cipla (Hauppauge, NY)
- …role ensures the integrity, accuracy, and completeness of batch records related to pharmaceutical manufacturing processes, providing assurance that products are ... authorities. Review, creation and revision of BPRs, SOPs, and other documents related to manufacturing processes. Ensure batch records are audit-ready and fully… more
- Cipla (Central Islip, NY)
- …are not limited to the following: Reviewing and confirming the compliance related to raw materials, in process and finished product analytical documents. Monitoring ... in the identified areas. Actively participating in review of data related to laboratory investigations and incidents and ensuring proper compliance. Performing… more
- Bayer (Buffalo, NY)
- …tomography (CT) and cardiovascular (CV) portfolio, including injectors, contrast media, and related software and workflow solutions. They generate demand for the CT ... outcomes;Bachelor’s or advanced degree in business, life sciences, engineering, or related discipline;Demonstrated track record of achieving sales targets in a… more
- Formation Bio (New York, NY)
- …review and approval of batch records, release testing, and other quality- related documentation. Foster a culture of continuous improvement and development within ... quality strategies that identify and address potential quality risks. Managing quality- related activities related to manufacturing, clinical trials, and… more
- Cipla (Hauppauge, NY)
- …actions and ensure proper follow-up. Generate and maintain quality reports related to packaging material management, inspection results, and audit findings. Ensure ... for accuracy and compliance. Knowledge of pharmaceutical industry regulations related to packaging, labeling, and product distribution. Educational Qualification:… more
- Cipla (Central Islip, NY)
- …for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. ... as communicated time to time by department management/designee. Participate in safety related programs and or safety teams as needed. Enforce and follow safety… more
- Cipla (Central Islip, NY)
- …for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process. ... as communicated time to time by department management/designee. Participate in safety related programs and or safety teams as needed. Enforce and follow safety… more
- Cipla (Central Islip, NY)
- …document in applicable Log Books Determine when to stop a line related to safety or quality. Operate automatic packaging equipment. Document packaging activities. ... Segregate waste products and materials. Return unused material/product. Participate in safety related programs and or safety teams as needed. Reconcile product bulk,… more
- Cipla (Central Islip, NY)
- …GMP documents Change control documents Review of system records Perform activities related to periodic audit trail review of all quality softwares, ensure compliance ... Qualifications/Experience Entry level position. Master's degree in chemistry, pharmaceutical or related field is required. May require 1+ years' experience in a… more
- Lundbeck (Poughkeepsie, NY)
- …2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience. Must demonstrate the intellectual capacity to ... Strong leadership through participation in committees, job rotations, panels and related activities. TRAVEL: Willingness/Ability to travel up to 30% - 40%… more
