Average salary: $262,500 /yearly
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- ...Job Description Job Description About the Opportunity: A fast-growing cannabis company is seeking an experienced Compliance Manager to oversee regulatory compliance across all aspects of our operations. This role is key to maintaining our standing with local...SuggestedFull timeLocal area
Cannabis Cartridge Company - unspecified
Tempe, AZ17 days ago - Job Description Associate Director Regulatory Affairs Our client is seeking an experienced Associate Director of Regulatory Affairs to lead clinical regulatory strategy for a portfolio of small-molecule drug programs progressing from late clinical development through...Suggested
Codon Partners
Boston, MA17 days ago $138.38k - $198.15k
...and technical studies. Lead permit strategy development and application processes with state and federal agencies. Manage compliance for linear infrastructure projects, including telecom and energy. Collaborate with Account Directors to expand ERMs footprint...SuggestedFull timeContract workFixed term contractCasual workWorldwideFlexible hoursERM
Walnut Creek, CA9 days ago$138.38k - $198.15k
...preparation of permit applications and negotiate conditions with applicable state and federal agencies. Direct permitting and compliance associated with telecom, energy infrastructure and other linear development projects with an emphasis on U.S. Army Corps of Engineers...SuggestedFull timeContract workERM
Walnut Creek, CA9 days ago$138.38k - $198.15k
...Lead permit strategy development and negotiate permit applications with state and federal agencies. Direct permitting and compliance for telecom, energy infrastructure and linear development projects, focusing on U.S. Army Corps of Engineers, California Coastal...SuggestedFull timeWorldwideERM
Pasadena, CA9 days ago$138.38k - $198.15k
...preparation of permit applications and negotiate conditions with applicable state and federal agencies. Direct permitting and compliance associated with telecom, energy infrastructure and other linear development projects with an emphasis on U.S. Army Corps of Engineers...SuggestedFull timeContract workShift workERM
San Jose, CA9 days ago$170k - $200k
Associate Director, Regulatory Affairs - San Diego, CA Mirador is a next-generation precision medicine company focused on immunology and inflammation. The companys Mirador360 precision development engine leverages the latest advances in human genetics and cuttingedge...SuggestedFull timeBioSpace
San Diego, CA2 days ago- ...and external stakeholders (including partners, CROs, CMOs, consultants, and contractors) in order to execute program objectives in compliance with applicable regulations What Knowledge & Experience youll bring to us Bachelor or Masters degree required Minimum of...SuggestedFull timeContract workFor contractorsLocal area
Nuvation Bio, Inc.
Boston, MA10 days ago $153.6k - $241.34k
...). Act as a strategic partner throughout the product lifecycle, from clinical development to marketing maintenance. Ensure compliance with EFPIA, IFPMA, FDA codes, and regulations. Minimum Qualifications: ~ BSc Degree (preferred) or BA. ~8+ years of pharmaceutical...SuggestedFull timeRemote workWorldwideTakeda
Boston, MA10 days ago$156k - $195k
...coordinate, author, and prepare regulatory submissions and work with Regulatory Operations in the electronic submission Ensure compliance with global regulatory requirements and adherence to internal policies and processes; coordinate global regulatory compliance...SuggestedFull timeWorldwideFlexible hoursSumitomo Pharma
Honolulu, HI10 days ago$164k - $205k
...Laboratory Developed Test (LDT) products, including labeling, promotional materials, product changes, and documentation required for compliance and regulatory approval. Monitor and report on international regulatory developments and LDT requirements that may...SuggestedFull timeLocal areaFlexible hoursGRAIL
Boston, MA8 days ago$160k - $275k
Associate Director or Director, Regulatory Affairs Kymera is a clinicalstage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients...SuggestedFull timeKymera Therapeutics
Boston, MA9 days ago$182.07k - $235.62k
Position Associate Director, CMC Regulatory Affairs Biologics Overview Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes medicines in areas of unmet medical need. We focus on HIV/AIDS, liver diseases...SuggestedFull timePart timeFor contractorsWorldwideGilead Sciences, Inc.
Foster, CA10 days ago$170k - $200k
A next-generation precision medicine company is seeking an Associate Director of Regulatory Affairs in San Diego, CA. This role develops and implements regulatory strategy while leading cross-functional teams in clinical trials. Candidates should have over 8 years of Regulatory...SuggestedFull timeMirador Therapeutics
San Diego, CA6 days ago$153.6k - $241.34k
...Provides strategic and tactical advice to teams to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. Is a leader both in the department and within R&D, contributing to cross-functional...SuggestedMinimum wageFull timeTemporary workLocal areaRemote workTakeda
Boston, MA10 days ago$10k
Overview The Associate Director, Regulatory Affairs will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for product development and approval, in alignment with the global business strategy. Responsible for leading ...Full timeTemporary workFor contractorsLocal areaBiogen
San Francisco, CA6 days ago$153.6k - $241.34k
...affairs for GI & Inflammation programs. Provides strategic and tactical advice, leads crossfunctional initiatives, and maintains compliance with regulatory requirements. Accountabilities Lead global regulatory strategies for complex or highly complex projects....Full timeRemote workTakedaPharmaceutical Nordics AB
Boston, MA3 days ago$159.7k - $199.6k
...CMC regulatory guidance and strategy including identifying and assessing/mitigating regulatory risks. Participates in ensuring compliance of CMC activities with applicable regulatory requirements. Evaluates manufacturing processes and changes, assesses the...Full timeWork at officeLocal areaRemote workWorldwideNight shift3 days per weekAcadia Pharmaceuticals Inc.
San Diego, CA9 days ago- ...developing global regulatory strategies for small molecule therapeutics, coordinating across multidisciplinary teams, and ensuring compliance with regulatory requirements. Candidates should possess a Bachelor's degree in a life science and at least 8 years of relevant...Full timeWork at office3 days per week
Acadia Pharmaceuticals Inc.
San Diego, CA9 days ago - ...Responsibilities Responsible for independently managing assigned CMC programs, including daily execution of plans, strategic activities, and compliance for clinical and commercial products. Lead the development, preparation and submission of the CMC dossiers, technical...Full timeWork at office
Alexion Pharmaceuticals
Boston, MA7 days ago $182.07k - $235.62k
...risk assessments on major global CMC regulatory issues. Provides regulatory assessments for manufacturing changes and quality compliance and participate in technical risk assessment exercises. Coordinates and facilitates development of Regulatory CMC strategies with...Full timeLocal areaGilead Sciences, Inc.
Foster, CA10 days ago$172k - $187k
...strategic regulatory direction and managing CMC related activities in close partnership with crossfunctional development teams, ensuring compliance with global regulatory standards and alignment with internal program goals. This position is eligible for a hybrid workplace...Full timeWork at officeLocal areaAlkermes
Boston, MA10 days ago- ...information and labeling documentation for all relevant Gilead products across our product portfolio to ensure Gilead's ongoing compliance with governing laws, regulations, and company policies and procedures. Product information and labeling documentation contains the...Full time
Gilead Sciences, Inc.
Foster, CA9 days ago $182.07k - $235.62k
...accurate and thorough input and recommendations into resource plans required to complete own deliverables. Track resources to ensure compliance with agreed resource allocation, including budgets. Ensure own work complies with established practices, policies and...Full timeFor contractorsLocal areaGilead Sciences, Inc.
Foster, CA9 days ago- Associate Director, Regulatory Affairs Advertising and Promotion Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across crossfunctional teams. RA Ad...Full timePart timeFor contractorsLocal area
Gilead Sciences, Inc.
Foster, CA9 days ago - ...a contract basis. The role offers flexible remote or hybrid options and involves leading regulatory submissions and maintaining compliance with global health authorities. Candidates should have over 8 years of regulatory experience in the pharmaceutical or biotech industry...Full timeContract workRemote workFlexible hours
Real Staffing
Boston, MA9 days ago - ...and external consultants/service providers in support of registration activities, and developing and maintaining documentation for compliance programs such as labeling, promotional material review and other regulatory requirements. Responsibilities Lead regulatory...Full timeRemote work
BD (Tissuemed Ltd)
San Diego, CA10 days ago - ...join our team on a contract basis. This role will support regulatory strategy and execution across development programs, ensuring compliance with global health authority requirements. The ideal candidate is a proactive problem-solver with strong leadership skills and...Full timeContract workRemote workFlexible hours
Real Staffing
Boston, MA9 days ago $185k - $250k
...functional Collaboration Partner with Process Development, Quality, Manufacturing, and Business Development teams to ensure regulatory compliance and readiness. Provide regulatory guidance during the design and construction of the GMP manufacturing facility. Compliance...Full timeTemporary workSummer holidayFlexible hoursCodexis, Inc.
Redwood City, CA7 days ago- Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic...Full timeWork at office
AbbVie
Chicago, IL4 days ago
