Alcon has announced three Regulatory Operations job openings in Bangalore within its Quality & Regulatory Affairs function. These opportunities are suitable for candidates interested in regulatory affairs, regulatory submissions, state licensing, regulatory information management, compliance, labeling, UDI, and regulatory documentation.

The three openings include Associate I, Regulatory Operations, Associate I, Regulatory Operations – State Licensing, and Associate II, Regulatory Operations. Selected professionals will support regulatory submissions, maintain regulatory databases and archives, prepare dossiers and licensing documentation, and help ensure compliance with applicable regulations and Alcon’s internal quality standards.

1. Associate I, Regulatory Operations

Job Requisition ID: R-2026-49220

The Associate I, Regulatory Operations role supports regulatory submission activities across Alcon franchises. The position involves dossier preparation, submission management, regulatory databases, publishing, licensing, labeling, archives, and technical file administration.

Key Responsibilities

• Support operational activities related to regulatory submissions.
• Prepare and manage regulatory dossiers and submission documentation.
• Maintain databases covering regulatory submissions and approvals.
• Support submission publishing, licensing, and labeling activities.
• Maintain Regulatory Affairs archives and technical files.
• File product notifications, applications, and relevant quality-testing information with regulatory agencies.
• Support product compliance with external regulations and internal standards.
• Review proposed regulatory changes and assist in assessing their business impact.
• Support and audit regulatory compliance processes.
• Provide regulatory guidance concerning product changes, labeling, literature, quality testing, and advertising.
• Follow applicable GxP requirements and company SOPs.
• Maintain complete and accurate regulatory documentation.

2. Associate I, Regulatory Operations – State Licensing

Job Requisition ID: R-2026-49183

This Regulatory Operations position focuses primarily on U.S. state licensing. The associate will support regulatory filings, applications, renewals, amendments, licensing databases, compliance records, and submission deadlines across U.S. jurisdictions.

Key Responsibilities

• Support activities involving U.S. state regulatory agencies and licensing requirements.
• Perform data entry, document preparation, record maintenance, and filing activities.
• Assist with applications, license renewals, amendments, discontinuations, and related regulatory filings.
• Maintain state license certificates, submission records, approvals, and licensing documentation.
• Track regulatory filing and licensing deadlines.
• Monitor submission status and help ensure timely completion.
• Work with Regulatory Affairs, Legal, Quality, Supply Chain, Commercial Operations, and other teams.
• Research applicable regulatory and licensing requirements.
• Support compliance with requirements including DSCSA, PDMA, FDCA, and state licensing regulations.
• Help improve regulatory data quality and operational efficiency.
• Maintain accurate documentation and comply with SOP and GxP requirements.

3. Associate II, Regulatory Operations

Job Requisition ID: R-2026-49237

The Associate II position involves more complex Regulatory Operations activities, including regulatory submissions, dossiers, publishing, licensing, labeling, technical files, compliance processes, and regulatory information management.

Key Responsibilities

• Manage complex regulatory operations activities and documentation.
• Support timely and accurate regulatory submissions.
• Maintain submission and approval databases.
• Prepare regulatory dossiers across different franchises.
• Support regulatory publishing, licensing, and labeling.
• Maintain Regulatory Affairs archives and technical file documentation.
• File notifications and applications with relevant regulatory agencies.
• Assess regulatory requirements and their potential business impact.
• Support implementation and auditing of regulatory compliance processes.
• Provide regulatory guidance to development and marketing stakeholders.
• Maintain accurate GxP documentation.
• Support quality control and continuous improvement activities.

Preferred Skills

Candidates with knowledge or exposure to the following areas may have an advantage:

• Unique Device Identification (UDI)
• GUDID
• EUDAMED
• Regulatory Information Management (RIM) systems
• Regulatory data governance
• Regulatory submissions and publishing
• Regulatory databases
• Medical device regulations
• GxP and SOP compliance
• Regulatory documentation
• Cross-functional stakeholder management
• Risk identification and issue resolution

Qualifications

Alcon has not specified a mandatory degree in these job descriptions. The company states that candidates should possess appropriate education and experience to successfully perform the responsibilities of the role.

Based on the regulatory, healthcare, medical-device, quality, and compliance nature of these positions, potentially relevant educational backgrounds may include:

B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Biomedical Science, Microbiology, Biochemistry, B.Tech/M.Tech Biotechnology, Biomedical Engineering, and other relevant science, healthcare, engineering, or regulatory-related degrees.

Important: This broader degree list is guidance based on the nature of the work and is not an official Alcon eligibility list. Candidates should rely on Alcon’s application screening criteria for final eligibility.

Skills Relevant to Alcon Regulatory Operations

Applicants can strengthen their profiles by demonstrating knowledge of regulatory affairs, dossier preparation, submission management, regulatory publishing, labeling, licensing, technical documentation, GxP, SOP compliance, document control, regulatory databases, UDI, GUDID, EUDAMED, RIM systems, and regulatory data governance.

Strong attention to detail, documentation accuracy, communication, organizational skills, deadline management, problem-solving, and the ability to collaborate with cross-functional teams are also highly relevant.

Salary for Alcon Regulatory Operations in Bangalore

Alcon has not disclosed salary information in the supplied job postings. For structured-data purposes, a reasonable market estimate for comparable Regulatory Operations positions in Bangalore may be approximately:

Estimated Salary: ₹4.5 lakh – ₹10 lakh per annum

Actual compensation can vary significantly according to the specific Associate I or Associate II position, relevant experience, education, regulatory expertise, internal compensation structure, and interview performance. This range should not be represented as an officially disclosed Alcon salary.

Benefits of Working in Regulatory Operations

These roles provide exposure to global Quality & Regulatory Affairs operations and can help professionals build experience across regulatory submissions, medical-device regulations, regulatory information management, licensing, labeling, UDI, data governance, and compliance.

Regulatory Operations experience can also support longer-term career progression into Regulatory Affairs, Regulatory Information Management, Regulatory Publishing, Regulatory Data Management, UDI, Labeling, Quality & Regulatory Compliance, and Regulatory Operations leadership positions.

How to Apply

Apply for Associate I – Regulatory Operations (R-2026-49220)

Apply for Associate I – State Licensing (R-2026-49183)

Apply for Associate II – Regulatory Operations (R-2026-49237)