Regulatory Affairs Professional

Regulatory Affairs ProfessionalThis role is responsible for leading the development and execution of regulatory strategies and documents in support of clinical trials and product registration.Key Responsibilities:Develop and implement regulatory strategies to ensure compliance with relevant regulations and guidelines.Prepare and review regulatory documents,...

Regulatory Affairs ProfessionalThe ideal candidate will be responsible for working closely with international regulatory teams to ensure compliance with Indian regulations.Develop and maintain in-depth knowledge of India's Medical Device Regulations (MDR).Collaborate with cross-functional teams to implement effective regulatory strategies.Identify and...

Regulatory Affairs SpecialistThis role is a great opportunity for individuals with a strong understanding of regulatory affairs and a passion for ensuring compliance. The Regulatory Affairs Specialist will play a critical role in assisting international regulatory teams with navigating evolving business needs in the Indian market.Key...

Job Title: Regulatory Affairs Specialist">Job Description:">We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to manage and support regulatory submissions, ensure compliance with global regulatory requirements, and maintain the highest standards of operational excellence in regulatory processes.">Technical skills: Deep...

Regulatory Affairs Specialist JobThis is a critical role in our organization, responsible for managing and supporting regulatory submissions to ensure compliance with global regulations.The ideal candidate will have a deep understanding of CDSCO regulations, including the Drugs and Cosmetics Act, 1940, and related rules, guidelines, and circulars.Key...

Position SummaryThe Regulatory Affairs Specialist will be responsible for managing regulatory activities for biosimilar products for the emerging market, with a strong focus on LATAM region. This role involves ensuring compliance with regional regulations, supporting product lifecycle management, and leading submissions for primary filings and variations in...

This role plays a pivotal part in bringing medical devices to market while ensuring ongoing compliance. Key responsibilities include participating on cross-functional teams, developing global regulatory strategies, authoring regulatory submissions, and interacting with regulatory agencies.The ideal candidate will have expertise in product development...

Position Summary The Regulatory Affairs Specialist will be responsible for managing regulatory activities for biosimilar products for the emerging market, with a strong focus on LATAM region. This role involves ensuring compliance with regional regulations, supporting product lifecycle management, and leading submissions for primary filings and variations...

Job Title: Regulatory Affairs Specialist Med/Pharma (Female)Location: Remote Position Overview: We are seeking an experienced Regulatory Affairs professional with expertise in both pharmaceutical and medical device regulatory compliance. The role involves preparing, reviewing, and submitting regulatory documentation to global health authorities, ensuring...

Regulatory Affairs ManagerWe are seeking an experienced Regulatory Affairs Manager to oversee and execute all regulatory activities for drug substances and products.