Global 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 AssociateThis is a critical role that involves providing regulatory support to various departments across the organization. The successful candidate will be responsible for ensuring that all regulatory activities align with business needs.Key Responsibilities:The Regulatory Affairs Associate will be responsible for:Providing regulatory...

Regulatory Affairs Manager RoleThis role is ideal for a highly motivated individual with strong knowledge of FDA CVM and EMA guidelines, experience with CMC registrations in the US and Europe, and excellent communication and organizational skills.The successful candidate will be responsible for developing regulatory strategies, overseeing submission...

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...

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...

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...

As a Regulatory Affairs Specialist, you will play a critical role in ensuring our products meet local and international standards. We seek a detail-oriented and proactive professional to support strategies, submissions, and compliance activities across global markets.Key Responsibilities:Regulatory Submissions & Approvals:Prepare, review, and submit...

RoleAPI Regulatory Affairs DMF Filing/ Compilation (Global market)Level Associate Manager / Manager Level:-Required Education/Exp :-Experience Req. : 11 yrs.18 yrs. Qualification:M.Sc. / M.PharmaResponsibilities1. Hands on Regulatory Affairs-API /DMF Filing/ DMF Compilation/ Submission/ Customer Communication etc.2. Compilation and submission of DMFs...

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...