Lead RA Work Flexibility: Onsite Key Areas of Responsibility: Translates regulatory intelligence into actionable local, regional, and global regulatory strategies aligned with business goals. Anticipates regulatory risks and emerging issues , offering proactive, solutions‑oriented guidance throughout the product lifecycle. Evaluates products for classification, jurisdiction, and market‑access requirements , identifying the most efficient regulatory pathways. Provides technical regulatory input across quality, preclinical, clinical, and manufacturing teams to ensure compliance. Leads regulatory submissions end‑to‑end —planning, preparing, submitting, and managing interactions with global health authorities. Reviews scientific documentation (quality, preclinical, clinical) for completeness, accuracy, and regulatory acceptability. Collaborates effectively with cross-functional teams , supporting meetings with regulatory authorities and advisory committees. Develops and enhances regulatory SOPs , strengthens compliance, and trains stakeholders on evolving regulatory expectations. Manages complex regulatory projects with autonomy, strong organization, and sound decision‑making. Demonstrates inclusive leadership , embracing diverse perspectives and supporting the development of Specialists/Sr. Specialists. Adapts to challenging assignments , navigates organizational dynamics, and continuously builds regulatory expertise. Qualifications Bachelor’s degree in Engineering, Science, or related field; Master’s in Regulatory Science preferred 4+ years of regulatory affairs experience in healthcare, medtech, pharma, or related regulated industries Regulatory Affairs Certification (RAC) is a plus Strong understanding of regulatory pathways, compliance, submissions, quality systems, and post‑market requirements Excellent communication, technical writing, and project management skills Ability to operate with autonomy, judgment, and cross‑functional influence Travel Percentage: 20% Experience Level Senior Level
ఇతర details
- It is a Full Time రిక్రూటర్ / హెచ్ఆర్ / అడ్మిన్ job for candidates with 4 - 6+ years Experience.
Lead Regulatory Affairs Specialist job గురించి మరింత
ఈ Lead Regulatory Affairs Specialist job కు అర్హత ప్రమాణాలు ఏమిటి?
Ans : అభ్యర్థులు అన్ని విద్యాస్థాయిలు అర్హత, 4-7 సంవత్సరాల అనుభవం కలిగి ఉండాలి, ఇది Stryker India Private Limited ఇచ్చే job, IMT Manesar, Gurgaon లో ఉంది.
ఈ Lead Regulatory Affairs Specialist job కు ఎంత జీతం ఉంటుంది?
Ans : Salary details will be shared during the hiring process.
ఈ job లో ఏ shiftఉన్నాయి?
Ans : ఈ job లో Day shift ఉంది.
ఈ job కోసం ఆఫీస్ కు వెళ్లాలా?
Ans : అవును, అభ్యర్థులు IMT Manesar, Gurgaon లోని ఆఫీస్ కు వెళ్లి పని చేయాలి.
ఈ Lead Regulatory Affairs Specialist job లో ఎన్ని vacancies ఉన్నాయి?
Ans : ఈ position కి 1 opening ఉంది.
ఈ job అన్ని genders కు అందుబాటులో ఉందా?
Ans : అవును, ఈ job పురుషులు మరియు మహిళలు ఇద్దరికీ అందుబాటులో ఉంది.
ఈ position యొక్క job location ఏమిటి?
Ans : ఈ position యొక్క job location IMT Manesar, Gurgaon.
ఈ Lead Regulatory Affairs Specialist job ను మంచి అవకాశంగా ఏమి చేస్తుంది?
Ans : The employer has not disclosed the salary for this role, but it is a Full Time opportunity with 1 opening.