Regulatory Affairs Job at Alcon | Chemistry Graduates Apply Now
Are you looking for a Regulatory Affairs Job or a CMC Job in the pharmaceutical industry? This is a great opportunity through Alcon Careers for the role of Senior Associate, Regulatory Affairs CMC in Bangalore. Ideal for candidates seeking an MSc Chemistry Job, this position offers exposure to global regulatory strategies, submissions, and compliance. If you are exploring Pharma Regulatory Jobs or Pharmaceutical Jobs, this role provides excellent career growth in regulatory affairs.
About Alcon
Alcon is a global leader in eye care and pharmaceutical innovation, dedicated to improving vision and enhancing quality of life. Through Alcon Careers, professionals can explore opportunities in Regulatory Affairs Jobs, CMC Jobs, and Pharmaceutical Jobs. The company develops advanced medical devices, pharmaceuticals, and surgical solutions for global markets. It offers an excellent platform for MSc Chemistry Job seekers to build careers in regulatory affairs and healthcare innovation. With a strong commitment to quality, compliance, and patient care, Alcon continues to lead the industry while providing excellent career growth opportunities in the pharmaceutical sector.
- Job Title: Senior Associate, Regulatory Affairs CMC
- Locations: Bangalore, India
- Job Requisition ID: R-2026-44755
Job Profile Summary
Develops and implements global
chemistry, manufacturing, and control (CMC) regulatory strategies throughout the lifecycle of biologics, pharmaceuticals, and devices. Prepares and directs the development of CMC submissions, including initial market registrations, progress reports, supplements, amendments, and/or periodic experience reports. Represents the company during communications and meetings with health authorities. Interacts and negotiates with regulatory agencies in order to expedite approval of pending registration and answer any questions. Participates in the identification of risk areas and develops alternative courses of action. Assesses the impact of new regulations and implements appropriate changes, leads the development of the company policy and positions on draft regulations and guidance.Job Description
This role is part of Alcon’s Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly. The Sr. Associate, Chemistry Manufacturing & Control (CMC) (Professional Path), is primarily responsible for supporting global CMC regulatory strategies and maintenance for biologics, pharmaceuticals, and devices. You will assist in preparing CMC submissions, support product registration preparation, and support and manage maintenance activities of approved products. You’ll also identify regulatory risks, develop alternative solutions, and assess new regulations for necessary changes.
Specifics Include:
- Support and manage registration maintenance activities for the approved products
- Assist in developing and implementing global CMC regulatory strategies for biologics, pharmaceuticals, and devices
- Help prepare CMC submissions, including market registrations, progress reports, annual reports, supplements, amendments, and periodic experience reports
- Participate in identifying risk areas and developing alternative courses of action
- Assess the impact of new regulations and implement necessary changes
- Adhere to GxP regulations by following SOPs, maintaining accurate documentation, ensuring quality control, and completing required training
- Meet individual job requirements and contribute to overall organizational compliance and continuous improvement with regulatory requirements
Qualifications: An associate shall have the appropriate education and experience to successfully perform the responsibilities/activities of this role.
