Senior Research And Development Executive

Saipro Industries

Pirangut

On-site

INR 600,000 - 900,000

Full time

7 days ago
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Job summary

Saipro Industries in India seeks a Regulatory and Quality Assurance professional to oversee R&D of nutraceuticals, health supplements, and instant premixes. The role focuses on overseeing NPD, regulatory requirements, testing schedules, and documentation as per FSSAI, Ayush, and external audits.

You will lead CAPA planning, implement FSSC 22000, HACCP, VACCP, WHO-GMP, and GHP programs, maintain audit readiness, and coordinate with customers on new product developments while safeguarding the

Qualifications

  • Experience with FSSAI and Ayush regulatory requirements.
  • Knowledge of record-keeping and documentation per FSSAI rules.
  • Experience implementing internal audits and quality assurance activities.
  • Strong CAPA planning and zero-defect mindset.
  • Ability to communicate with team and management.
  • Excellent organizational and time-management skills.

Responsibilities

  • 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.

Skills

Regulatory compliance
Quality assurance
Documentation
CAPA
Audits
FSSAI
NPD oversight
GMP
HACCP
FSSC 22000

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.
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