- Tris Pharma (Monmouth Junction, NJ)
- …limited to: procurement, enforcement, monetization, etc.Registered to practice before the United States Patent and Trademark Office (USPTO)Current, hands-on ... Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned US biopharmaceutical company with a focus on development and commercialization of innovative… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Head of Compliance as part of the Global Quality team based in ... Raritan, NJ. Role OverviewThe Head of Compliance will be responsible for...audit program.Schedule, execute, report and follow-up on internal and US and Global external audits (travel required).Ensure audit observations… more
- Aequor (Framingham, MA)
- …or FDA -regulated environment a mustNice to have: Previous experience with Veeva, quality agreements, supplier compliance , supplier change notifications preferred ... the MA BioCampus, ensuring excellence in quality standards and regulatory compliance across external partnerships. This role requires leading Supplier Change… more
- Cipla (Fall River, MA)
- …supervisor position is an individual contributor role and reports to the Head Quality Assurance Analytical for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary ... include but are not limited to the following: Confirming and ensuring the compliance of the protocols and reports of method validations / verifications / comparison… more
- Legend Biotech USA, Inc. (Dallas, TX)
- …ethical standards and will adhere to the regulatory requirements of the FDA and other government agency guidelines, without exception. This position will report ... directly to the Head of Sales.This position will work within the following...in the event that performance improvement is not achieved.Ensure compliance , without exception, with all corporate policies and procedures… more
- Cipla (Fall River, MA)
- …in a pharmaceutical environment is responsible for managing controlled documents to ensure compliance with GMP, GDP, and regulatory standards such as FDA 21 ... Any other work assigned by Operation Lead, QMS Lead, Head Unit Quality Assurance and Quality Head ....in the key markets of India, South Africa, the US , and other economies of the emerging world. Cipla… more
- Cipla (Fall River, MA)
- …schedules of projects. Monitor packaging processes for adherence to cGMP, FDA , and Cipla's quality standards. Identify and resolve operational inefficiencies, ... standard operating procedures (SOPs) Monitor operational metrics such as efficiency, compliance rates, and resource utilization. Identify areas for improvement in… more
- Cipla (Fall River, MA)
- …safe and efficient execution of their job duties, while ensuring product compliance to established standards. Essential Duties and Responsibilities : Responsible for ... cGMP policies, documentation and record keeping in accordance with industry and FDA standards and Safety and sanitation regulations. Performs a combination of manual… more
- CSL Behring (King Of Prussia, PA)
- The Head of Global Regulatory Affairs - Advertising and Promotion is responsible for leading and overseeing the regulatory strategy and compliance of promotional ... company policies. The incumbent will provide leadership across regions (eg, US , EU, APAC, LATAM) and collaborate with cross-functional partners including Marketing,… more
- BeOne Medicines (Emeryville, CA)
- …affairs, legal, healthcare compliance and other business functions primarily in the United States with some activities globally to ensure compliance with ... **General Description:** This role is the head of Promotional Regulatory, and provides regulatory leadership, support, oversight, and strategic guidance on… more
- embecta (Parsippany, NJ)
- …channels on? LinkedIn ,? Facebook ,? Instagram ?and?X (http://twitter.com/embecta) .? **Why join us ?** A career at embecta means being part of a team that values ... varying needs of our diverse and global employees. The ** Head of Internal Audit** is a key member of...with a focus on financial integrity, operational efficiency, regulatory compliance , and enterprise risk management. As a senior leader… more
- Endo International (St. Louis, MO)
- …of manufacturing sites in the area of Quality Systems, and Training. + Interfaces with FDA and regulatory agencies outsite the US for events that include but are ... **Why Us ?** We want the best and brightest people...The Sr. Director, Quality is responsible for ensuring cGMP compliance and product quality at the Saint Louis, MO… more
- Endo International (Webster Groves, MO)
- **Why Us ?** We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our ... Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone...The main result of the incumbent is to ensure compliance with cGMP, regulatory and internal requirements regarding the… more
- ITG Brands (Greensboro, NC)
- …and nicotine products. The ideal candidate will bring deep expertise in FDA regulation, multi-state compliance , and regulatory litigation, with the ability ... industry (tobacco, pharmaceuticals, medical devices). + Strong background in FDA regulatory matters, state-regulatory compliance , regulatory litigation, FOIA.… more
- CSL Behring (King Of Prussia, PA)
- …GRA. With support, engaging with health authority (HA) in stationed country ( FDA or EMA), maintaining productive relationship with HA contacts and driving positive ... to product health authority interaction with support GRL or Regulatory TA Head . Partner with GRAST members to achieve regulatory deliverables (including leading… more
- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …Pharma has established itself as a leading player in the generics market in the US , and we are rapidly ramping up our presence in the specialty branded market with ... Device Specialist II** , you will support the QA Head in ensuring that all medical devices and combination...and enhancing our **Quality Management System (QMS)** , ensuring compliance with global regulatory requirements, and preparing the site… more
- J&J Family of Companies (Santa Clara, CA)
- …Category:** People Leader **All Job Posting Locations:** Santa Clara, California, United States of America **Job Description:** **POSITION SUMMARY** Robotics ... of Johnson & Johnson Medtech Surgery Group, seeks a Head of Quality and Compliance for the...requirements, and supporting the Regulatory Affairs team to ensure compliance with FDA , EU MDR, and other… more
- Stanford Health Care (Palo Alto, CA)
- …current job openings. Your best is waiting to be discovered. Day - 10 Hour ( United States of America) Head /Neck Advanced Practice Provider (APP) Job ... wish to work in Oncology, with a sub-specialty in Head /Neck Medical Oncology, we are actively recruiting for 2...Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA -approved… more
- Genentech (South San Francisco, CA)
- **The Position** **The Opportunity** The Head of US Medical Population Science & Health (USM PS&H) will lead the CMG US Medical Population Science & Health ... team reporting to the VP Head of US Medical. This role is...economic environments impacting Roche/Genentech, coupled with thorough knowledge of US regulatory/ FDA requirements. + Scientific credibility and… more
- J&J Family of Companies (Titusville, NJ)
- …- MD **Job Category:** People Leader **All Job Posting Locations:** Raritan, New Jersey, United States of America, San Diego, California, United States ... health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are... of America, Titusville, New Jersey, United States of America **Job Description:** At Johnson & Johnson… more
