Redica Systems is hiring for a Data Solutions Coordinator – Regulatory Intelligence in India. The role is suitable for professionals with experience in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence, particularly within the pharmaceutical, biologics, medical device, or animal health sectors.
Job Title: Data Solutions Coordinator – Regulatory Intelligence
Company: Redica Systems
Location: HSR Layout, Bengaluru, Karnataka, India
Work Arrangement: Remote work available
Employment Type: Full-time
Experience: 4+ years preferred
Qualification: Master’s degree in Regulatory Affairs, Pharmaceutics, or Quality Assurance preferred
Industry: Pharmaceutical, Biologics, MedTech, Animal Health
Author: PharmaBharat Editorial Team
About Redica Systems
Redica Systems is a data and analytics SaaS company focused on regulatory and quality intelligence for regulated industries. The company develops technology-enabled intelligence solutions that help organizations monitor regulatory changes, understand their impact, and manage compliance risk.
Redica states that it was founded in 2010 and has developed an intelligence platform serving pharmaceutical, biopharmaceutical, medical device, food, and cosmetics organizations. Its current platform combines regulatory, inspection, enforcement, and other intelligence data to help quality and regulatory teams make informed decisions.
Redica Systems Data Solutions Coordinator Job Description
The Data Solutions Coordinator – Regulatory Intelligence will work with the Regulatory Intelligence team to monitor regulatory developments across global markets.
The position involves identifying regulatory updates, assessing their operational and strategic impact, determining the industries affected, and accurately structuring regulatory intelligence data within Redica’s platform.
This is a multidisciplinary role combining regulatory affairs, GxP knowledge, regulatory intelligence, data classification, and technology-enabled data operations.
Key Responsibilities
- Monitor regulatory authorities across more than 150 countries for relevant regulatory developments.
- Track updates affecting pharmaceutical, biologics, medical device, and animal health sectors.
- Analyze regulatory changes and determine their industry scope and practical impact.
- Distinguish actionable regulatory changes from informational updates.
- Classify regulatory intelligence using appropriate industry and GxP categories.
- Extract important metadata such as effective dates, consultation deadlines, and enforcement timelines.
- Link related regulatory documents and maintain structured regulatory intelligence records.
- Monitor evolving global regulatory frameworks and identify emerging regulatory trends.
- Collaborate with internal teams to improve monitoring scope and classification logic.
- Perform quality checks to maintain data accuracy and integrity.
- Monitor KPIs related to regulatory intelligence and data operations.
- Identify opportunities to improve regulatory intelligence workflows and structured data processes.
Qualifications and Eligibility
Candidates applying for the Redica Systems Data Solutions Coordinator job should ideally have:
- Around 4 years of experience in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence.
- Experience in the pharmaceutical, biologics, medical device, or animal health industry.
- Strong knowledge of GxP principles and global regulatory frameworks.
- Ability to interpret regulatory documents and understand their practical industry impact.
- Experience analyzing regulatory updates, compliance information, or regulatory documentation.
- Strong attention to detail and data accuracy.
- Good analytical and decision-making skills.
- Ability to communicate regulatory information clearly.
- Familiarity with technology and data operations.
- A Master’s degree in Regulatory Affairs, Pharmaceutics, or Quality Assurance is preferred.
Key Skills Required
Regulatory Intelligence | Regulatory Affairs | GxP | Quality Assurance | Pharmaceutical Regulations | Regulatory Data | Data Classification | Regulatory Compliance | Data Analysis | Metadata Management | Global Regulatory Frameworks | Data Quality | Process Improvement
Who Can Apply?
This opportunity may be relevant for experienced professionals working in:
- Regulatory Affairs
- Regulatory Intelligence
- Quality Assurance
- GxP Compliance
- Pharmaceutical Regulatory Operations
- Medical Device Regulatory Affairs
- Biologics Regulatory Affairs
- Animal Health Regulatory Affairs
- Regulatory Data Operations
Candidates should carefully compare their experience and qualifications with the employer’s requirements before applying.
Work Location
The listed office location is:
Floor 4, 147 17th Cross Road, 9th Main Road, opposite Allen Solly, Sector 6, HSR Layout, Bengaluru, Karnataka, India.
The job description also states that employees can work remotely.
Redica’s corporate information confirms that the company has a Bangalore, India presence and describes its workplace as hybrid, with employees distributed globally.
Salary
Salary: Not disclosed in the provided job description.
For accuracy, PharmaBharat does not attribute an estimated salary to Redica Systems as an employer-provided salary. Candidates should confirm the compensation package directly during the recruitment process.
Why This Role Is Relevant for Regulatory Professionals
The position combines conventional regulatory intelligence activities with structured data operations. Candidates will not only monitor regulatory changes but also classify them, extract metadata, assess applicability, and maintain high-quality structured information.
Redica’s regulatory intelligence platform currently describes functionality around regulatory monitoring, classification by GxP and other categories, impact assessment, document versioning, and integration with enterprise systems.