Hetero Hiring Pharmacy Graduates | QC Chemist Role
Looking for a pharma fresher job in the pharmaceutical industry? This latest QC Chemist Jobs opportunity is an excellent choice for candidates with a B.Pharm, M.Sc. Analytical Chemistry or Organic Chemistry background. The role involves API quality testing, HPLC, GC, FTIR, UV-Vis analysis, GMP/GLP compliance, documentation, and stability studies. If you are eager to build a rewarding career in pharmaceutical quality control, don’t miss this exciting pharma freshers job offering valuable hands-on laboratory experience through QC Chemist Jobs.
About the Company
Hetero is a leading pharmaceutical company based in India, specializing in the development and manufacturing of generic medicines and active pharmaceutical ingredients (APIs). With a commitment to quality and innovation, Hetero operates in various therapeutic segments and aims to provide affordable healthcare solutions globally. The organization is known for its rigorous adherence to quality standards, making it an excellent choice for those pursuing qc chemist jobs.
Job Details
- Position: QC Chemist
- Location: Nakkapally, Anakapali, Andhra Pradesh, India
Job Description
The QC Chemist will be responsible for ensuring the quality of raw materials, intermediates, and finished products through rigorous testing and analysis. The role involves performing various chemical and physical tests, documenting results, and ensuring compliance with regulatory standards. This position is crucial for maintaining the high-quality standards that Hetero is known for in the pharmaceutical industry.
Key Responsibilities
- Perform sampling of raw materials, intermediates, and finished Active Pharmaceutical Ingredients (APIs) according to standard procedures.
- Conduct routine and non-routine chemical and physical tests to ensure quality standards are met.
- Analyze products using techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis spectroscopy, FTIR, and other analytical instruments.
- Accurately document all analytical results and observations in laboratory notebooks or electronic systems.
- Prepare and review certificates of analysis (CoA) for finished products and intermediates.
- Ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) in all documentation.
- Adhere to established quality standards as per pharmacopeias (USP, BP, IP, EP, etc.) and regulatory guidelines.
- Participate in internal and external audits and implement corrective actions where required.
Eligibility Criteria
- Education: Master’s degree in Analytical Chemistry, Organic Chemistry, or B. Pharmacy.
- Technical Skills:
- Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR, and titration.
- Familiarity with laboratory software such as Chromeleon, LabSolutions, or Empower.
- Understanding of GMP, GLP, and regulatory requirements.
- Soft Skills:
- Strong analytical and problem-solving abilities.
- Attention to detail and commitment to quality.
- Effective communication and documentation skills.
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