The Quality Control Specialist - HPLC position at Cropel Lifesciences Pvt. Ltd. in Chhatral is a full-time role that involves managing and performing HPLC analyses to ensure the highest standards of quality control and support quality assurance initiatives. Your responsibilities will include conducting QC tests, interpreting test results, maintaining lab equipment, adhering to Good Manufacturing Practice (GMP) guidelines, and contributing to quality audits. It is essential to document and report findings accurately and promptly. To excel in this role, you should possess skills in Quality Control and Quality Assurance, along with experience in Quality Management and Quality Auditing. Proficiency in GMP standards, strong analytical and problem-solving abilities, attention to detail, and excellent documentation skills are also crucial. A Bachelor's degree in Chemistry, Biochemistry, or a related field is required, while previous experience in the pharmaceutical or biotech industry would be advantageous. Additionally, good communication and teamwork skills will be beneficial for collaborating effectively in this role.,
As a Quality Control Specialist - HPLC at Cropel Lifesciences Pvt. Ltd., located on-site in Chhatral, your role will involve performing and managing HPLC analyses to ensure the highest standards of quality control. Your responsibilities will include carrying out QC tests, interpreting test results, maintaining lab equipment, adhering to Good Manufacturing Practice (GMP) guidelines, and supporting quality assurance initiatives. Additionally, you will be involved in assisting in quality audits and accurately documenting and reporting findings. Key Responsibilities: - Perform and manage HPLC analyses - Conduct QC tests and interpret test results - Maintain lab equipment - Adhere to Good Manufacturing Practice (GMP) guidelines - Support quality assurance initiatives - Assist in quality audits - Document and report findings accurately and promptly Qualifications: - Quality Control and Quality Assurance skills - Experience with Quality Management and Quality Auditing - Proficiency in Good Manufacturing Practice (GMP) - Strong analytical and problem-solving abilities - Attention to detail and excellent documentation skills - Bachelor's degree in Chemistry, Biochemistry, or a related field - Previous experience in a pharmaceutical or biotech industry is a plus - Good communication and teamwork skills,