- Curaleaf (Ravena, NY)
- …a meaningful impact, drive innovation, and help shape the future of cannabis. Manager , Operations Location: Ravena, NY - On-site About the Role: As an Operations ... Manager at Curaleaf, you'll be the driving force behind...and compliant facility, ensuring all equipment and spaces meet cGMP standards Create and manage production schedules and inventory… more
- Cresilon, Inc. (Brooklyn, NY)
- …matter expert in areas including polymer material science, formulation strategies, analytical chemistry , and biomaterial interactions with biological systems. ... Learn more about the company at www.cresilon.com. The R&D Formulation Manager /Principal Scientist will lead the design, development, and implementation of novel… more
- Aquestive Therapeutics (Portage, IN)
- …drug product manufacturing as a lead role (Director, Associate Director or Sr. Manager ). Deep understanding of cGMP , ICH guidelines, USP requirements and ... Raw Material Test Program, Stability Program, Environmental Monitoring Program and Analytical Method Transfer Program. Provide expertise, direction and resources for… more
- curium (Noblesville, IN)
- …supporting policies, programs and procedures as directed by the Health Physics Manager or designee. The successful candidate will oversee the Radiation Safety ... on-call rotation. Essential Functions As assigned by the Health Physics Manager , supervise Radiation Safety Technicians and their day-to-day operations. Must… more
- Novo Nordisk (Bloomington, IN)
- …help us make what matters. The Position Responsible for leading the QC Chemistry department to ensure fulfillment of departmental targets in accordance with the Novo ... compliance with applicable regulations & SOPs. Manage the Site QC Chemistry Laboratory testing, processes & personnel. Relationships Reports to Director. Essential… more
- AbbVie (North Chicago, IL)
- …regulatory policies and government regulations. Qualifications + Bachelors, Masters, or Ph.D. in Analytical Chemistry typically with a minimum of 14 (BS), 12 ... experience. + Direct people-management experience. + Strong technical background in analytical chemistry , excellent analytical problem-solving skills.… more
- Cambrex High Point (Charles City, IA)
- … Development, Chemical Development, Process Support Group and Quality Control. + Perform analytical chemistry assays based on new and existing methodologies + ... materials. + May also perform other duties as required. Qualifications/Skills Analytical Chemistry Knowledge : Beginning to demonstrate an understanding… more
- Cambrex High Point (Minneapolis, MN)
- … Development, Chemical Development, Process Support Group and Quality Control. . Perform analytical chemistry assays based on new and existing methodologies . ... materials. . May also perform other duties as required. Qualifications/Skills Analytical Chemistry Knowledge: Strong understanding of the fundamentals of… more
- Cambrex High Point (Minneapolis, MN)
- … Development, Chemical Development, Process Support Group and Quality Control. . Perform analytical chemistry assays based on new and existing methodologies . ... reference materials. . May also perform other duties as required. Qualifications/Skills Analytical Chemistry Knowledge: Good understanding of the Principles of … more
- Cambrex High Point (Charles City, IA)
- … Development, Chemical Development, Process Support Group and Quality Control. + Perform analytical chemistry assays based on new and existing methodologies + ... reference materials. + May also perform other duties as required. Qualifications/Skills Analytical Chemistry Knowledge : Strong understanding of the fundamentals… more
- Cambrex High Point (Durham, NC)
- …+ Some supervisory experience in a laboratory environment is highly desired. + Strong analytical chemistry knowledge and an SME in at least one functional area ... for drug substance and drug product. Reporting to the ( Manager , Associate Director, or Director), the Analytical ...+ cGMP knowledge with experience in RCA + Strong familiarity… more
- CoreRx (Clearwater, FL)
- …Performs relevant QC testing, such as HPLC, GC, Dissolution, Malvern and wet chemistry testing as required in compliance with cGMP requirements, compendia ... resume. Thank you for choosing CoreRx as your employer of choice. DESCRIPTION The Analytical Chemist II is an integral part of the team, contributing to our success… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …managing and conducting activities related to current Good Manufacturing Practice ( cGMP ) site audits, quality control and manufacturing (QCM) product documentation ... to promote engaged, collaborative, and results-driven work environments. _The Senior Manager , Verification Programs has the following responsibilities:_ * Leads the… more
- Cambrex High Point (Longmont, CO)
- …or MS in Chemistry or related field and 8+ years in cGMP chemical manufacturing environment with increasing responsibility + At least 3+ years supervisory ... and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years… more
- Catalent Pharma Solutions (Harmans, MD)
- **Senior Manager , CAPA** **Summary:** _Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... and life-saving treatments for patients annually._ _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the… more
- DuPont (Hemlock, MI)
- …healthcare market quality requirements (including Current Good Manufacturing Practice [ cGMP ] standards). This person will provide leadership while maintaining ... ISO-13485:2016, etc.) are implemented and maintained in accordance with cGMP (US 21 CFR 820) and FDA regulations. +...in a technical field of study (eg: Industrial Engineering, Chemistry , etc.). + Relevant credentials (eg: ISO Lead Auditor… more
- Fujifilm (College Station, TX)
- **Position Overview** **_Summary_** **:** The Quality Assurance Program Quality Manager (QA PQM) is responsible for the operational oversight and execution of ... in close collaboration with cross-functional teams, the Program Quality Manager helps ensure successful program outcomes through detailed coordination, compliance… more
- Catalent Pharma Solutions (Baltimore, MD)
- **Job Title:** Sr. Manager Upstream Process Development **City:** Baltimore **State** : MD **JOB DESCRIPTION** : + Lead the client projects starting from the ... development and optimization toward cGMP manufacturing for clinical trials, registration, or improvements of...and compliant laboratory work environment: coordinate with the EHS manager to implement EHS initiatives; work with team leaders… more
- Cambrex High Point (Waltham, MA)
- …at Snapdragon Chemistry , a Cambrex company, to ensure compliance with cGMP and internal quality standards. + Maintain and manage the Quality Management System ... across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. With over 40 years...career where You Matter by applying today! About Snapdragon Chemistry Snapdragon Chemistry was acquired by Cambrex… more
- Bristol Myers Squibb (Indianapolis, IN)
- …with RayzeBio policies, standards, procedures and global current Good Manufacturing Practice ( cGMP ). The Senior Manager provides Quality support and oversight ... RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Senior Manager , QA for QC is responsible for quality oversight of the Quality Control… more
