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Production and Qc Chemist
2 weeks ago
**Position**: Production and QC Chemist
**Location**:Nagole, Telangana
**Department**: Production and Quality Control
**Experience**:10 years
**Education**: Graduate/Postgraduate in Pharmacy or Life Sciences
**Industry**: Formulations, Veterinary Health Care, Pharmaceuticals
**Job Summary**:
**Key Responsibilities**:
**1. Production Oversight**:
- Manage and supervise the production of pharmaceutical formulations, ensuring adherence to GMP and standard operating procedures (SOPs).
- Collaborate with the production team to optimize workflow and ensure product quality during each stage of production.
- Monitor equipment, raw materials, and processes to ensure smooth and efficient production operations.
**2. Quality Control**:
- Develop, implement, and oversee quality control systems for testing raw materials, in-process samples, and finished products.
- Conduct routine QC tests in accordance with established protocols, analyzing test data to verify product quality.
- Ensure proper documentation and reporting of QC results in compliance with regulatory standards.
**3. Compliance and Documentation**:
- Ensure compliance with GMP, safety, and environmental regulations throughout the production process.
- Maintain accurate production records and QC documentation, including batch records, test reports, and deviations.
- Lead investigations into any quality-related issues and implement corrective and preventive actions (CAPA).
**4. Team Management**:
- Provide training and guidance to junior chemists, production staff, and QC personnel.
- Coordinate with the R&D, supply chain, and regulatory departments to ensure seamless communication and efficient processes.
**5. Process Improvement**:
- Identify areas for process optimization, cost reduction, and efficiency improvement in production and QC.
- Stay updated on the latest industry trends, technologies, and regulatory changes to ensure continuous improvement.
**Key Skills and Qualifications**:
- Graduate/Postgraduate degree in Pharmacy or Life Sciences.
- Minimum 10 years of experience in pharmaceutical formulations and GMP.
- Strong knowledge of pharmaceutical production processes, equipment, and quality control techniques.
- Experience in handling regulatory audits and compliance with quality standards (e.g., WHO GMP, ISO).
- Proficiency in using analytical instruments such as HPLC, GC, and UV-Vis Spectrophotometer.
- Excellent problem-solving, communication, and leadership skills.
- Ability to work independently and as part of a team in a fast-paced, dynamic environment.
**Benefits**:
- Competitive salary and benefits package.
- Opportunity for career advancement in a growing industry.
- Professional development and training opportunities.
Pay: ₹15,000.00 - ₹25,000.00 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
Supplemental Pay:
- Overtime pay
**Education**:
- Bachelor's (required)
**Experience**:
- Quality control: 1 year (required)
- Quality assurance: 1 year (required)
- Leadership: 1 year (required)
Work Location: In person