- Merck & Co. (North Wales, PA)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... data governance reviewsThe Global Clinical Data Standards (GCDS) Data Standards Specialist may contribute to the definition and maintenance of business processes… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Specialist , Manufacturing Automation ( Hybrid ) g, quality and engineering groups.- -Supports a large spectrum of sophisticated ... within Manufacturing Operations; providing multiple opportunities to learn new automatioThe Specialist is a member of the Focus Factory Automation team responsible… more
- Merck & Co. (Philadelphia, PA)
- Job DescriptionThe Associate Specialist of Regulatory Planning & Publishing works closely with various stakeholders of regulatory and safety submissions to ... job role skills and regulatory knowledge. Shared Services: ( Regulatory Submission Specialist )-Provide regulatory submission/systems support.-Manage … more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must actively support, participate and embrace an empowered team culture… more
- Merck & Co. (Durham, NC)
- …with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract ... and attendant quality control problems. Basic understanding of GMPs and of regulatory requirements as they apply to the vaccine, sterile pharmaceutical or related… more
- Merck & Co. (Rahway, NJ)
- …Maintains personal awareness of developments in the fields of medical information, regulatory policy , adverse event reporting, information storage and retrieval, ... Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and… more
- Merck & Co. (Rahway, NJ)
- …CCDS, CCPPI, CCIFU) and US labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of the EU Labeling and other ... and implementing US Labeling for assigned products in line with regulatory requirements and internal standards and guidelines.- Assisting with developing and… more
- Merck & Co. (Rahway, NJ)
- …dedicated colleagues while developing and expanding your career.The Senior Trial Initiation Specialist in Global Site Budgets and Payments will be responsible for ... and presentation skills.Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines which includes knowledge of Standard of Care/Routine Care and… more
- Merck & Co. (Durham, NC)
- …with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract ... be responsible for activities that support Good Manufacturing Practice and regulatory compliance during product manufacturing within the respective VMF's to include… more
- Merck & Co. (Durham, NC)
- …Durham employs 1,000+ people. This role as a Training Operations Associate Specialist will be an energetic individual with strong interpersonal, leadership, and ... manufacturing and related systems (ie SAP) Familiarity with pharmaceutical regulatory requirements Project management and data analysis skillsTechnical writing… more
- Merck & Co. (Rahway, NJ)
- …Pharmacology and Pharmacometrics --Immune/Oncology-(QP2-IO)-team in the role of-Senior Specialist .--QP2-IO team is part of the Global Clinical Development ... senior scientists you will develop a comprehensive understanding of global regulatory expectations for small molecules and biologics, including support and authoring… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the ... project level in developing and executing regulatory strategy and compliance plans to promote and support...1-2 indirect reports. This position will work on site Hybrid in Franklin Lakes, NJ three days per week.… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- **Job Description Summary** The Senior Regulatory Affairs (RA) Specialist within the BD Interventional Surgical Devices Business unit will work on regulatory ... for the development of complex global regulatory strategies and preparation of regulatory submissions. The Senior RA Specialist will provide regulatory … more
- BD (Becton, Dickinson and Company) (Covington, GA)
- **Job Description Summary** As Regulatory Affairs Specialist II, you will be responsible for the implementation of strategies including domestic and ... and other product project team supports. This is a hybrid position where the candidate is required to be...possible** with us. **Key responsibilities will include:** + Provide regulatory support through the product life cycle on product… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** As Staff Regulatory Affairs Specialist , Infusion, you will be responsible for Regulatory Affairs projects within the Medication ... Management Systems Infusion portfolio. Regulatory Affairs activities, will include: development, execution and management of submissions, development and review of… more
- Southern California Edison (Rosemead, CA)
- Job Description **Join the Clean Energy Revolution!** Become an **Energy Policy , Pricing, & Customer Analytics Sr Specialist ** at Southern California Edison ... distributed energy resources, microgrids, and building electrification). As an **Energy Policy , Pricing, & Customer Analytics Sr Specialist ,** your work… more
- Eversource Energy (East Berlin, CT)
- The Accounting Specialist for Accounting Research is responsible for performing research, documenting conclusions, and maintaining all accounting policies and ... but not limited to complex contracts, new and/or unusual transactions, and regulatory outcomes\. This position will assist with renewable energy accounting matters,… more
- Merck (West Point, PA)
- **Job Description** The Manufacturing Execution System (MES) Specialist acts as a subject matter expert and an area(s) site MES key point of contact, for Operations ... areas utilizing electronic Master Batch Records. The MES Specialist 's primary responsibility is to ensure that the deployment of the Korber PAS-X electronic Master… more
- Merck (Durham, NC)
- **Job Description** **Position Description: Specialist , Manufacturing Automation ( Hybrid )** g, quality and engineering groups. Supports a large spectrum of ... within Manufacturing Operations; providing multiple opportunities to learn new automatio The Specialist is a member of the Focus Factory Automation team responsible… more
- Merck (North Wales, PA)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... governance reviews + The Global Clinical Data Standards (GCDS) Data Standards Specialist may contribute to the definition and maintenance of business processes… more
