- Merck & Co. (Rahway, NJ)
- …modelers, and colleagues in other related function areas. Primary Activities :Prepare compliant programming code for regulatory submissions including ... analysis/modeling datasets, tables, listings, figures and associated documentationEnsure programmatic traceability from data source to analysis/modeling resultSupport the development of programming standards to enable efficient and high-quality production of… more
- Aequor (Athens, GA)
- …monitoring equipment. Utilize standard operating procedures to conduct environmental monitoring activities . Use data management systems to enter and track results. ... Demonstrate a visible & tangible commitment to HSE. In addition to the above, other assigned duties & projects deemed appropriate within the position scope. Able to operate assigned lab equipment. May order supplies needed in the labs. May assist in… more
- Merck & Co. (North Wales, PA)
- …modelers, and colleagues in other related function areas. Primary Activities :Prepare compliant programming code for regulatory submissions including ... analysis/modeling datasets, tables, listings, figures and associated documentationEnsure programmatic traceability from data source to analysis/modeling resultSupport the development of programming standards to enable efficient and high-quality production of… more
- Merck & Co. (Rahway, NJ)
- …collaborative relations with other groupsDirect support of validation activities and compliance-related requirements functions.Willing to constructively challenge ... the status quo and explore continuous improvement opportunitiesStrong abilities in Stakeholder Management and building and strengthening cross-functional networksExcellent communication skills Preferred Experience and Skills: Experience with Operational… more
- Lundbeck (Poughkeepsie, NY)
- …leadership through participation in committees, job rotations, panels and related activities . TRAVEL: Willingness/Ability to travel up to 30% - 40% domestically ... to (a) regularly meet/interact with customer base and internal personnel within assigned territory; and (b) typically attend 4-8 internal/external conferences and meetings spanning locations within the United States. Travel must be able to be completed in a… more
- Cipla (Fall River, MA)
- …and software programs. Strong knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, ... analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP), USP monograph requirements. Technical Knowledge and Computer Systems Skills Understanding of laboratory… more
- Cipla (Fall River, MA)
- …quality assurance (QA). Strong knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug ... products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good Distribution Practices (GDP), etc. Technical Knowledge and Computer Systems Skills Understanding of machines used in pharmaceutical… more
- Merck & Co. (North Wales, PA)
- …and can be located in the United States or Europe (EMEA). - Primary activities include, but are not limited to: Leadership - As a procurement leader, participates ... in development and implementation of business strategy and ensures delivery of required business performance.- The Director of Packaging will have a vision and strategy for the short and long-term success of the category. The incumbent will be expected to act… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …OverviewThe Operations Process Trainer will be responsible for performing training activities for Operations team members who support cGMP Clinical and Commercial ... Cell Therapy Manufacturing. This individual will partner with Training team members in collaboration with management in Operations to support personalized cell therapy production through safe and compliant operations according to cGMP requirements. This… more
- Lundbeck (Bothell, WA)
- …relevant regulatory requirements. Support Process Sciences in technology transfer activities to GMP manufacturing facilities, ensuring compliance with regulatory ... standards. Required Education, Experience, and Skills: Accredited bachelor's degree in Biochemistry, Biotechnology, Chemical Engineering, or a related field 10+ years of relevant experience within the biotechnology or pharmaceutical industry. Experience in… more
