- Charles River Laboratories (Rockville, MD)
- …build a career that you can feel passionate about. **Job Summary** The Associate Director Quality is responsible for partnering with functional stakeholders at ... leadership and strategic direction to operate with and maintain compliance to regulatory and industry quality standards in support of existing and new cell-based… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …true to the best of my knowledge. **Job Description** About the role: As the Associate Director of Process Engineering, you will be member of the engineering ... time-efficient, innovative design solutions that meet user, safety, quality, and regulatory requirements. + Oversee and review feasibility studies, design packages,… more
- Publicis Groupe (New York, NY)
- …present in more than sixty countries with over 23,000 employees worldwide. **Overview** The Associate Director of Business Affairs is an integral part of the ... content. In particular, identify risk relating to intellectual property, the regulatory environment, SAG-AFTRA Union regulations etc., Ensure agency best practices… more
- Carrier (Indianapolis, IN)
- …. **About this role:** The ** Associate Director , Environmental Health ... and in compliance with local, state, and national requirements or any other regulatory agency rules and regulations. + Lead process of reviewing and approving safety… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . **Position Summary:** We are seeking an experienced Associate Director , Customer Experience (Cx), Patient & Care Partner ... access measures, digital engagement). + Monitor industry trends, competitor offerings, and regulatory changes in the behavioral health market. + Build and nurture… more
- Citigroup (New York, NY)
- …tactics, and driving marketing innovation. We are seeking a highly experienced SEM Associate Director to join our Paid Search Activation team. This individual ... Lead to ensure all SEM activities adhere to stringent internal policies and regulatory requirements. Assist in building and enforcing a standardized QA framework. +… more
- Lilly (Indianapolis, IN)
- …to enable the making of medicine "with safety first and quality always". As Associate Director in Lilly's IT group partnering with Engineering and Global ... Tech at Lilly collaborations. + Ensure that all solutions adhere to regulatory , compliance, and security standards, including GxP, ensuring data and system… more
- Otsuka America Pharmaceutical Inc. (Madison, WI)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of clinical ... are manufactured, packed, labelled, stored, and transported accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role has… more
- Takeda Pharmaceuticals (Boston, MA)
- …DP/PKG** **Location: Cambridge, MA** **About the role:** As a Process Scientist ( Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), ... and the life cycle management of existing products. You will lead regulatory interactions, including the preparation of Chemistry, Manufacturing, and Controls (CMC)… more
- Lilly (Indianapolis, IN)
- …have a focus on minimizing the impact to our environment. **Position Brand Description:** The Associate Director will play a critical role in leading the site IT ... and innovation in manufacturing operations + Ensure compliance with regulatory requirements and industry standards in all digital transformation initiatives… more
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