Director, Product Development Salary at Adare Pharmaceuticals Inc BETA

Who We Are: TransPerfect was founded with a mission to help the world's businesses navigate the global marketplace. Today, we have grown to be an industry leader organization by helping clients globalize their business no matter what service they might need. TransPerfect provides a full array of language and business support services, including translation, multicultural marketing, website globalization, legal support, and any kind of technology solution. What You Will Be Doing: This role reports to the Solutions Engineering Team Lead as well as the Director of Application Development. Solutions Engineers (SEs) at TransPerfect are passionate about product development, client requests for enhancements and the resolution of production issues. Work with Client Service Representative and Solutions Engineer to resolve Trial Interactive Operations Escalations Assist with data migration with pre-defined utilities and processes Assist with PDC and IQ test scripts preparation and the execution

Position Title: Director, Regulatory, CMC Reports to: ED, Regulatory Affairs Location: Hybrid, Princeton, NJ PMV is seeking an experienced and motivated Director of Regulatory Affairs CMC (Chemistry, Manufacturing, and Controls) to lead the development and execution of CMC regulatory strategy for the Company’s assets. The Director, Regulatory Affairs-CMC will work closely with cross-functional teams, including other Regulatory functions, CMC, Quality Assurance, and external vendors) to ensure the successful submission of CMC dossiers and compliance with regulatory guidelines across regions throughout the product lifecycle. Responsibilities Act as Regulatory CMC Lead: Serve as the primary interface between CMC subject matter experts (SMEs) and Regulatory Affairs. Coordinate and lead all CMC regulatory projects, including budget, timelines, and CMC submission planning, ensuring all deliverables are met on time and within scope. Manage Regulatory CMC contractors/consultants to ensure acti

Reports to: Director, GMP Quality Assurance Location: Princeton, NJ (hybrid) This role is responsible for providing GMP QA expertise, oversight, and auditing support of contract manufacturing organizations of small molecule, oral dosage formulations. Additionally, this role supports PMV’s GxP procedures program, document control, and training activities, utilizing an electronic document management system. Responsibilities Support GMP QA activities spanning across CMC (Chemistry, Manufacturing & Controls) for drug substance, drug product, and clinical trial material, for all outsourced GMP activities. Ensure all API, drug product and packaged and labelled investigational material meet GMP regulations, as applicable to phase of development, and are released in a timely manner. Collaborate with CMC, Clinical Supplies Management, Regulatory Affairs, and other departments to resolve quality issues and implement process improvements. Review and approve GMP-related documents, including master

Are you an entrepreneur, passionate about innovation ? Founded in 1993, ALCIMED is an Innovation and New Business consulting company, specializing in innovative sectors: life science (food, biotech, healthcare), energy, aeronautics, chemistry, cosmetics, materials, space and defense. Our mission is to help our clients in the private and public sectors to explore and develop their uncharted territories including new technologies, innovative products and services, new usages and business models, innovation management, new geographies, and possible futures… We are a team of 200 people with degrees from the best universities and international schools, most possessing a dual background in science and business. We have five offices in Europe, one in the United States and one in Asia. Why Should you join us? Because you are passionate about exploring and developing unchartered territories in Life Sciences (pharmaceuticals, medical devices, biotech firms); Because you will generate and develop

Are you an explorer and interested in Sciences, Technology and Innovation? Founded in 1993, ALCIMED is an Innovation and New Business consulting firm, specializing in innovative sectors: life science (food, biotech, healthcare), energy, aeronautics, chemistry, cosmetics, materials, space and defence. Our mission is to help our clients in the private and public sectors to explore and develop their uncharted territories including new technologies, innovative products and services, new usages and business models, innovation management, new geographies, and possible futures… We are a team of 200 people with degrees from the best universities and international schools, most possessing a dual background in science and business. We have fiveoffices in Europe, one in the United States and one office in Asia. What you will do Under the supervision of a Project Manager: You will be in charge of the end-to-end completion of projects, from information-gathering to the drafting and presentation of

Job Type Full-time Description TerraCycle Overview TerraCycle is an international leader in innovative sustainability solutions, creating and operating first-of-their-kind platforms in recycling, recycled materials, and reuse. Operating in 20 countries, including 12 in Europe, TerraCycle works with manufacturers, retailers and end users to implement turnkey recycling programs through a range of public-facing services for hundreds of everyday waste streams that other waste management companies are unable to recycle. In 2019, TerraCycle introduced Loop - a platform that allows brands, retailers and consumers to move from a disposable to durable supply chain, enabling consumers to responsibly shop for a wide variety of commonly used products in reusable packaging. Since its debut, Loop has developed into the leading global reuse platform and is available in France, the United States and Japan. TerraCycle and Loop have received hundreds of awards and recognitions and have been highlighted

Job Type Full-time Description Summary: The Alumni Engagement Operations Associate is responsible for managing logistics and providing operational support for all in-person, virtual, and hybrid events (approximately 80-100 annually) organized by the Alumni & Development Office. This includes Alumni Weekend, Hill Weekend, affinity gatherings, and other alumni and development programming. This team member will provide event operations support, handle administrative tasks, and work closely with the Director of Alumni Engagement, colleagues, and external vendors to ensure seamless event execution. Additionally, this role supports the creation of alumni event communications and manages alumni event invitation lists to ensure effective outreach. The Alumni Engagement Operations Associate may be required to travel locally and attend certain events in person. Essential Responsiblities Event Logistics: Execute a 12-month production plan for Alumni Weekend, Hill Weekend, and Affinity Alumni Week

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Our Product Development Operations team drives strategic busine