- Takeda Pharmaceuticals (Concord, NH)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic ... Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, you… more
- Takeda Pharmaceuticals (Concord, NH)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible ... You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met for… more
- Takeda Pharmaceuticals (Concord, NH)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
- Bristol Myers Squibb (Devens, MA)
- …standards, and comparability studies. In addition, the ASL Associate Director will be accountable for enabling regulatory filings (analytical related), ... in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** ASL Associate Director , Analytical Strategy & Lifecycle Group Lead… more
- Takeda Pharmaceuticals (Concord, NH)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
- Merck (Concord, NH)
- …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
- Merck (Concord, NH)
- …Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- AbbVie (Waltham, MA)
- …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Medical Director provides specialist medical/scientific strategic and ... management plans. Responsible for routine and adhoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse Events (AE's)… more
- Kelly Services (Burlington, MA)
- **Sr. Manager/ Associate Director - Quality Assurance** **Burlington, MA** **Direct Hire** **Compensation: $125k-165k base + 10-15% annual bonus** **Candidate ... Quality function. This individual will report to the Sr. Director of Global GCP/GLP compliance and while...US. + Lead and participate in third party and regulatory audits including preparation and responses. + Oversee qualification… more
- Takeda Pharmaceuticals (Lexington, MA)
- …is true to the best of my knowledge. **Job Description** The Associate Director , Clinical Research provides clinical project management and leadership ... applicable internal legal and compliance policies as well as external US-specific regulatory guidelines. + Partners with US Medical TA leadership to determine… more
- Ford Motor Company (Concord, NH)
- …ready to change the way the world moves? **In this position ** As the Associate Director of M&A Integration, you will lead the strategic integration of merged ... smooth transition. + Ensure that all integration activities comply with regulatory requirements and company policies. + Drive synergy identification and realization,… more
- …included, respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to ... of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a...- Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio… more
- Bristol Myers Squibb (Devens, MA)
- …within the department and with Manufacturing, Quality Control, Quality Assurance, IT, global master data management, and Global Supply Chain organizations to ... reliable batch records and supporting data. + Collaborate with other stakeholders ( global and site) to maintain and optimize product hierarchy while maintaining… more
- Bristol Myers Squibb (Devens, MA)
- …one or more areas (ie, research, analytical, quality, engineering, manufacturing, regulatory CMC, or IT). + Proven ability to understand complex processes/problems ... propose alternate solutions (required based on need to design and implement global business processes and policies, which requires critical thinking and analysis… more
- Bristol Myers Squibb (Devens, MA)
- …pharmaceutical manufacturing to cGMP standards including extensive knowledge of regulatory guidelines and validation practices + Working knowledge of pharmaceutical ... + Knowledge of suppliers, industry trends and emerging players in global pharmaceutical manufacturing services + Strong presentation and communication skills both,… more
- Veralto (Waltham, MA)
- …That is the tomorrow Veralto is creating today. Veralto is a $4.8B global leader in essential technology solutions. Our industry-leading companies are building on a ... and authenticate the billions of goods that travel the global supply chain every day. And our Water Quality...**About The Role** Veralto is looking for a Senior Director of Strategic Development to contribute to the corporate… more
- Marriott (Concord, NH)
- …with the Global Information Security team and ensure that all regulatory standards and followed and implemented. The leader also set up governance, policy, ... **Position Type** Management **JOB SUMMARY** Marriott International (MI) is transforming its global network technology to offer the most advanced, most secure, most… more
- AbbVie (Waltham, MA)
- …multiple driver indications within a Therapeutic Area and supports the Manager ( Global Regulatory Lead (GRL), Associate Director , or Director ), in ... Description Responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or… more
- embecta (Andover, MA)
- …validation of electromechanical medical devices developed by embecta. Reporting to the Associate Director , R&D - Verification and Validation, the successful ... embecta is a global diabetes care company that is leveraging its...requirements are satisfied to all relevant Quality System and regulatory requirements. + Defines and leads the execution of… more
- embecta (Andover, MA)
- …of electromechanical medical devices developed by embecta. Reporting up to the Associate Director , R&D - Verification and Validation, the successful candidate ... embecta is a global diabetes care company that is leveraging its...requirements are satisfied to all relevant Quality System and regulatory requirements. + Definesand leads the execution of a… more