 Medical Affairs Job at Reckitt
Looking for exciting Jobs in Gurugram with a leading global healthcare company? Reckitt Careers has opened an excellent Medical Affairs Job opportunity for professionals from healthcare, medical, pharmacy, and life science backgrounds. This role offers the chance to work at the intersection of medical science, research, innovation, and consumer healthcare while contributing to the development of safe, effective, and scientifically substantiated products used by millions worldwide.
About the Company:
Reckitt is one of the world’s leading health, hygiene, and nutrition companies, home to some of the most trusted consumer healthcare brands globally. Driven by its purpose to protect, heal, and nurture, Reckitt combines scientific expertise, innovation, and consumer insights to create products that improve lives every day. Through its global Research & Development network, the company continues to advance healthcare solutions while maintaining the highest standards of quality, safety, and regulatory compliance.
Job Details:
- Job Role: GCMA Senior Associate – Germ Protection
- Location: Gurugram, Haryana
- Department: Research & Development (R&D)
Job Description:
Under the latest Reckitt Careers opportunity, the organization is hiring a Medical Affairs professional to support medical science activities within its Research & Development division. The role involves working closely with brand teams, regulatory experts, clinical researchers, quality specialists, and external stakeholders to generate medical evidence, support innovation projects, substantiate product claims, and contribute to scientific strategy. This Medical Affairs Job is ideal for candidates interested in consumer healthcare, medical research, clinical evaluation, scientific communication, and product innovation. The position is based in Gurugram and offers exposure to global healthcare projects and multidisciplinary collaboration.
Key Responsibilities for Medical Affairs Job:
- Lead medical representation on assigned category projects.
- Support medical affairs activities and scientific dossier development.
- Act as a subject matter expert in skin health, germ protection, cosmetics, and biocides.
- Drive execution of evidence-generation and medical strategies.
- Support product innovation and pipeline development.
- Provide scientific input for claims substantiation and competitor claim assessments.
- Collaborate with Regulatory, Safety, Quality, Clinical Research, Marketing, and R&D teams.
- Prepare clinical overviews, efficacy summaries, safety summaries, and medical documentation.
- Conduct systematic literature reviews and scientific evaluations.
- Support global product registration activities.
- Respond to medical information requests and provide scientific guidance.
- Ensure that medical and scientific documentation remains accurate and up to date.
- Support interactions with healthcare experts and key opinion leaders.
Educational Requirements:
- Bachelor’s Degree in Medical Sciences, or a related field.
- Postgraduate qualification preferred.
- Additional qualifications in clinical research, medical affairs, scientific writing, or healthcare innovation are advantageous.
Skills Required for Medical Affairs Job:
- Strong scientific and medical knowledge.
- Expertise in literature review and scientific evaluation.
- Medical writing and documentation skills.
- Understanding of healthcare regulations and compliance requirements.
- Clinical and scientific data interpretation abilities.
- Strategic thinking and business awareness.
- Project management and organizational skills.
- Excellent written and verbal communication skills.
- Leadership and stakeholder management capabilities.
- Ability to manage multiple projects simultaneously.
- Strong collaboration and teamwork skills.
Preferred Experience:
- Experience in medical affairs within pharmaceutical, healthcare, or consumer health industries.
- Experience in preparing scientific and medical documentation.
- Knowledge of cosmetics, germ protection products, and consumer healthcare categories.
- Experience in systematic reviews and scientific data appraisal.
- Understanding of clinical research and product development processes.
- Familiarity with healthcare regulations and compliance requirements.
- Exposure to product innovation and commercialization projects.
