LUMBAR HEALTHTECH PVT LTD

Role Overview: As a Regulatory Affairs Specialist, you will be responsible for preparing, submitting, and managing regulatory documentation and applications to ensure the approval of products. Your role will involve monitoring regulatory changes, communicating with authorities, and ensuring compliance with standards throughout the product lifecycle. Key Responsibilities: - Prepare and submit regulatory applications for timely approvals. - Stay informed about regulatory changes in various regions. - Interact with regulatory authorities and address their queries. - Verify product labeling and packaging compliance. - Maintain records of submissions, approvals, and correspondence. - Provide regulatory guidance to support product development. - Collaborate with internal teams to ensure compliance at all stages. Qualifications Required: - 1-3 years of experience in regulatory affairs or a related field. - D Pharm / M Pharm degree in life sciences, pharmacy, or a related discipline. - Familiarity with regulatory guidelines and standards. - Strong attention to detail and organizational skills. - Effective communication and problem-solving abilities. Company Details: Omitted as no additional details about the company are provided in the job description. Job Types: Full-time, Permanent Work Location: In person,