- Cipla (Central Islip, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate II AQA FLSA Classification: Professional, Exempt Work Location: Central Islip, NY ... but are not limited to the following: Scope: The Analytical Quality Assurance (AQA) associate II O III position is an team or individual contributor role and reports… more
- Cipla (Fall River, MA)
- …are not limited to the following: Scope : The Analytical Quality Assurance (AQA) associate I position is an team contributor role and reports to the Supervisor ... laboratory activities in areas such as active pharmaceutical ingredients ( API ), drug products, analytical development, Quality Control (QC), Good Laboratory… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the full ... - Required Experience and Skills: Minimum of five (5) years of manufacturing , technology, laboratory, and/or quality operations experience within GMP environment GMP… more
- Cipla (Fall River, MA)
- …8:30AM - 5:00PM (may vary based on business needs) Reports To : Manufacturing Manager Salary Range: $62,400 - $75,400 Purpose: The content and statements documented ... Invagen Pharmaceuticals is searching for experienced candidates for the position of Manufacturing Validation Engineer . The Manufacturing Validation Engineer is… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …API Process Engineering, you will be Takeda's global expert for small-molecule API manufacturing processes across batch and continuous platforms. You will ... and external CMOs. How you will contribute Lead the Small Molecules API Manufacturing Sciences activities within Global Process Science, serving as expert for… more
- Novo Nordisk (Clayton, NC)
- …in the production of ingredients for Novo Nordisk's innovative oral products. At API , you'll join a global network of manufacturing professionals who are ... of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable… more
- Otsuka America Pharmaceutical Inc. (Salem, OR)
- Job Summary The Associate Director, Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at CMOs ... Assurance support, including oversight of upstream and downstream biologics manufacturing processes, ensuring compliance with biologics-specific GMP requirements. This… more
- Deloitte (Minneapolis, MN)
- …off-shore technologists and vendor relationships. You will be part of API management strategies to enable seamless communication between applications. You will ... Develop and implement solutions that adhere to established enterprise architecture frameworks. API Management: Design, build, and manage APIs using API … more
- Novo Nordisk (Clayton, NC)
- …Team Novo Nordisk and help us make what matters. The Position Operate API manufacturing equipment to achieve production goals. Relationships Reports to Shift ... of ingredients for Novo Nordisk's innovative oral products. At API , you'll join a global network of manufacturing...Qualifications + High school graduate or equivalent required + Associate 's Degree or higher in Tech, Science, or Engineering… more
- Lilly (Indianapolis, IN)
- …requirements have been met prior to batch release. + Provide quality support of API manufacturing with the focus on holistic review of key activities associated ... the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization ( API -EM) that delivers a diverse...medicines essential to our patients around the world. The API EM Quality Associate provides support to… more
- Lilly (Indianapolis, IN)
- …third-party partners. Job Responsibilities: + Lead and manage quality aspects of external API manufacturing sites, including but not limited to batch record ... or related field. + Minimum of 5-8 years (Senior Associate ) or 8+ years (Principal Associate ) of...pharmaceutical or biopharmaceutical industry, with a strong focus on API manufacturing and external supply. + In-depth… more
- Lilly (Indianapolis, IN)
- …or commercialization / technical agenda projects + Deep technical knowledge of bulk API manufacturing equipment and unit operations. + Demonstrated ability to ... solutions to support communities through philanthropy and volunteerism. **Responsibilities:** The Associate Director - API EM Engineering Leader for Peptides… more
- Lilly (Lebanon, IN)
- …better for people around the world. _Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN ... API ). This facility is Lilly's largest investment in manufacturing capacity and is intended to provide APIs for...Purpose and Objectives of Position:** The Sr. Principal HSE Associate /Engineer is part of the Lilly Lebanon API… more
- Lilly (Lebanon, IN)
- …process chemistry + Demonstrated basic knowledge in small molecule, peptide, or oligonucleotide API Manufacturing . + Relevant industrial experience in any of the ... following discipline such as API Manufacturing , TS/MS (Technical Services/ Manufacturing Sciences), Quality Control, Quality Assurance, or Development. +… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …API Process Engineering, you will be Takeda's global expert for small-molecule API manufacturing processes across batch and continuous platforms. You will ... external CMOs. **How you will contribute** + Lead the Small Molecules API Manufacturing Sciences activities within Global Process Science, serving as expert for… more
- Takeda Pharmaceuticals (Boston, MA)
- …Authorities. **How will you contribute:** + Lead the Global Process Science, Small Molecules API Manufacturing Science team and serve as Takeda's expert on small ... following activities, along with Pharmaceutical Sciences and/or Operation Units: API Manufacturing Process Characterization, Technology Transfer from/to external… more
- Lilly (Indianapolis, IN)
- …#WeAreLilly **Responsibilities:** The Associate Director - Quality Assurance (QA) API External Manufacturing is responsible for managing the activities of ... support activities, implementation of Quality projects, technology transfers, and commercialization. The API EM QA Associate Director is responsible for quality… more
- Lilly (Lebanon, IN)
- …advanced manufacturing facility for production of Active Pharmaceutical Ingredient ( API ) molecules located in Lebanon, Indiana, USA. This facility is Lilly's ... the culture to enable a successful startup into GMP manufacturing operations. **Position Description:** The ** Associate Director...and resilience as the site grows to full scale API GMP manufacturing through start up. **Responsibilities:**… more
- Lilly (Houston, TX)
- … sites. These brand-new facilities will utilize the latest technology for API Manufacturing and will include several platforms including Peptides, Small ... of medicine "with safety first and quality always". The Associate Director for MQ Tech@Lilly will be part of...+ Position will be based out of a new API Lilly Manufacturing site in either Texas… more
- Lilly (Lebanon, IN)
- …better for people around the world. _Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. ... facility and the culture to enable a successful startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical… more
