Research And Development Officer

Saipro Industries; Pirangut; On-site; INR 600,000 - 900,000; Full time

Job summary

Saipro Industries in Maharashtra seeks a Regulatory Affairs & Quality Assurance professional to oversee NPD and regulatory compliance for nutraceuticals, health supplements, and dietary products. You will coordinate audits, maintain FSSAI and Ayush documentation, and drive CAPA for zero-defect production.

You will implement standards like FSSC 22000, HACCP, VACCP, and WHO-GMP while ensuring confidentiality of formulations and timely reporting to management.

Qualifications

• Oversee regulatory requirements for nutraceutical products.
• Maintain documentation per FSSAI and Ayush norms.
• Implement CAPA and ensure zero-defect processes.
• Coordinate external audits and internal quality programs.
• Drive adherence to FSSC 22000, HACCP, VACCP, WHO-GMP, GHP.

Responsibilities

• Overlook NPD & regulatory requirements of all products.
• Develop testing schedules & implement as per plan.
• Regulatory compliance for FSSAI & external audits.
• Maintain records and documentation per rules.
• Address customer complaints and plan CAPA actions.
• Ensure proper recall tracking and record-keeping.
• Formulate reports to track progress and QA activities.
• Maintain secrecy of formulation and R&D work.

Skills

Regulatory compliance

Documentation

CAPA management

Audit coordination

NPD coordination

Team communication

Time management

Confidentiality

Job description

• Research And Development of Nutraceuticals / Health Supplements / Dietary Supplements / Instant Premixes.
• Overlook NPD & regulatory requirements of all products.
• Developing testing schedules & implementation as per schedule.
• Responsible for Regulatory requirements of FSSAI & External audits.
• Develop strategies to improve the production process.
• Coordination with all customers for new product developments & regulatory requirements.
• Make sure whether the product goes through auditing and testing
• Responsible for record keeping and documentation as per FSSAI rules & regulations & Ayush.
• Take a look at customer complaints, implementation of CAPA, plan strategies to achieve zero defect product.
• Ensure that appropriate records are maintained and that a well-documented tracking and recall program exists.
• Make sure whether all the legal standards are met and review thoroughly the existing policies and standards
• Formulate timely reports and documentation to track progress.
• Make documentation of internal audits and quality assurance activities.
• Active participant of team for implementation of FSSC 22000, HACCP, VACCP, WHO-GMP, GHP.
• Eyeing on the objectives to maximize the profitability of the organization.
• Must be able to communicate effectively with team members and management.
• Must have superior organizational and time management skills.
• Responsible for maintaining secrecy of all formulation & research and development work.