IPL Biologicals - Senior Manager/Manager - Regulatory Affairs

IPL Biologicals is currently seeking a highly skilled and experienced Sr. Manager/Manager Regulatory Affairs to join our team. This critical role will be responsible for ensuring compliance with all applicable regulatory requirements for our biological products. The successful candidate will have a strong understanding of regulatory guidelines and requirements, exceptional leadership and strategic planning skills, as well as the ability to work effectively in a fast-paced and dynamic environment.

Job Title: Sr. Manager/Manager Regulatory Affairs

Location: [Location]

Key Responsibilities:

1. Develop and implement regulatory strategies and plans to support the development, registration, and commercialization of biological products in various global markets.

2. Ensure that regulatory submissions, including but not limited to INDs, BLAs, and post-approval submissions, are in compliance with relevant regulations and are of the highest quality.

3. Serve as the primary point of contact for regulatory agencies and lead interactions, meetings, and negotiations with regulatory authorities.

4. Keep abreast of changes in regulatory requirements and guidelines and advise internal teams on potential implications and necessary actions.

5. Provide regulatory guidance and support to cross-functional teams, including R&D, clinical, quality, and commercial teams, to ensure alignment with regulatory requirements and expectations.

6. Conduct regulatory assessments and gap analyses to identify potential issues and develop risk mitigation plans.

7. Collaborate with internal and external stakeholders to ensure that regulatory milestones and objectives are met on time and within budget.

8. Manage and mentor a team of regulatory affairs professionals, providing leadership, guidance, and support to ensure high performance and professional development.

Qualifications:

1. Bachelor's degree in a scientific or related field; advanced degree preferred.

2. A minimum of 8 years of regulatory affairs experience in the biopharmaceutical industry, with a focus on biological products.

3. Strong understanding of regulatory requirements and guidelines, including FDA and EMA regulations.

4. Proven track record of successful regulatory submissions and interactions with regulatory agencies.

5. Excellent communication, leadership, and project management skills.

6. Ability to work effectively in a cross-functional team environment and influence decision-making.

IPL Biologicals offers a competitive salary, comprehensive benefits package, and opportunities for professional growth and development. If you are a dedicated and experienced regulatory affairs professional looking to make an impact in the biopharmaceutical industry, we encourage you to apply for this exciting opportunity.

To apply for this position, please submit your resume and cover letter to [contact information].

We look forward to welcoming a talented and passionate Sr. Manager/Manager Regulatory Affairs to our team at IPL Biologicals.

Roles and Responsibilities:

- Has Done 9 (3) registrations under Insecticides Act, 1968

- Strong understanding of the Registration process and functioning of CIB.

- Prompt in responding to queries raised.

- Managing the registrations process on a day to day basis

- Producing reports and metrics from the database on upcoming registrations

- Maintaining up to date knowledge of registration requirements

- Liaising with clients as needed and work with datelines to achieve tasks.

- Good understanding of Regulations and guidelines (CIB, OECD, US EPA, EC), registration procedures and data requirements.

- Preparation of dossiers for global registration.

- Liaising with private institutions/ GLP laboratories and universities for data generation.

- Preparing various technical information e.g. Public health vector control, Agricultural pest control, Physico-Chemical properties, Labels, MSDS , Specification, Toxicological & Eco toxicological data, Bio efficacy, Persistency & Residue, Environmental fate, & data gap analysis etc. required for the products registration as per required regulatory guidelines.

- Coordinating with foreign clients, consultants for registration updates

Educational Qualification - Post Graduate

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