QA-ra Executive

6 days ago

Delhi Delhi, India Naturmed Scientific Full time

**1)**ABOUT US**:
NaturMed Scientific specializes in the development, manufacturing, and supply of high-quality natural plant-based ingredients and extracts for the dietary supplement, pharmaceutical, food, beverage, and sports nutrition industries. We offer a wide range of products, from plant extracts, carotenoids, CO2 extracts, essential oils, oil powder, and fruit powders.

NaturMed Scientific is constantly innovating and developing research-based natural ingredients that improve people's quality of life amid rapidly changing lifestyles. We are committed to developing sustainable processes and relationships across the entire supply chain that allow us to deliver the highest quality ingredients sourced sustainably and ethically.

**2)**COMPETENCE REQUISITES**:
**A) QUALIFICATIONS**:Bachelors in Life Sciences/Pharma/Biotechnology

**B) EXPERIENCE** Fresh graduate or up to 1 year.

**C) SKILLS REQUIRED**:

- Bachelor’s degree in a relevant discipline such as Life Sciences, Chemistry, Biology, or Food Science.
- Fresh graduate or up to 1 year of experience in Quality Assurance and Regulatory Affairs, preferably within the herbal and nutraceutical industry, with exposure to certification processes.
- Understanding of industry-specific certifications, standards, and regulatory requirements**.**:

- Excellent analytical and problem-solving abilities.
- Foundational experience or basic understanding on managing audits, including liaison with certification bodies.
- Effective communication and interpersonal skills.
- Familiar with European (EU) and United States Pharmacopoeia (USP) Standards.
- Proficient in Microsoft Outlook, Word, and Excel.
- Ability to identify and resolve quality-related issues.

**3) ROLES & RESPONSIBILITIES**:

- Monitor and stay up-to-date with industry-specific certifications and regulatory standards, implementing necessary updates to ensure ongoing compliance.
- Coordinate and facilitate both internal and external audits, ensuring comprehensive evaluation of quality systems, processes, and documentation.
- Prepare technical documentation in accordance with international market regulations, including Technical Data Sheets (TDS), Certificates of Analysis (COA), Material Safety Data Sheets (MSDS), product specifications, and other relevant technical materials.
- Develop and compile technical documentation required for export consignments.
- Provide technical support and prepare quality-related documents as requested by the sales team for customer requirements.
- Manage the preparation and dispatch of product samples for laboratory analysis.
- Assist in the development of country-specific regulatory dossiers.
- Support the creation and maintenance of Standard Operating Procedures (SOPs), Hazard Analysis and Critical Control Points (HACCP) plans, and Corrective and Preventive Action (CAPA) documentation in response to deviations and customer complaints.
- Identifying and assessing regulatory risks and developing strategies to mitigate them
- Collaboration with Cross-functional Teams

**Job Types**: Full-time, Permanent

**Benefits**:

- Health insurance

Schedule:

- Morning shift

Application Question(s):

- Do you have a Bachelors degree in a relevant discipline such as Life Sciences, Chemistry, Biology, or Food Science?

Work Location: In person

**Speak with the employer**
+91 8448354526

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