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Pharma Quality Control Officer - Min 1 Year Experienced, must have HPLC instrument Knowledge
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Lezivia Lifesciences
Job Description
Company Description Lezivia Lifesciences is a well-established pharmaceutical company recognized for delivering high-quality products to patients. Most of its portfolio is manufactured at WHO-approved facilities, ensuring stringent compliance with international quality standards. The company focuses on reliability, safety, and consistency across its product range. Lezivia Lifesciences values professionals who are committed to quality and continuous improvement in pharmaceutical manufacturing. The organization offers an environment where quality-focused individuals can contribute to patient well-being and professional growth.
Role Description This is a full-time, on-site role based in Amritsar for a Pharma Quality Control Officer with a minimum of 1 year of experience and hands-on HPLC instrument knowledge. The role involves performing routine and non-routine quality control tests on raw materials, in-process samples, and finished products using HPLC and other analytical instruments. The officer will prepare, review, and maintain test reports, ensure adherence to standard operating procedures and regulatory guidelines, and support investigations of deviations or non-conformities. Daily responsibilities include calibrating instruments, maintaining laboratory records, collaborating with quality assurance and production teams, and contributing to continuous improvement of testing methods and quality standards. The role requires strict compliance with safety protocols and GMP practices within the laboratory environment.
Qualifications
Role Description This is a full-time, on-site role based in Amritsar for a Pharma Quality Control Officer with a minimum of 1 year of experience and hands-on HPLC instrument knowledge. The role involves performing routine and non-routine quality control tests on raw materials, in-process samples, and finished products using HPLC and other analytical instruments. The officer will prepare, review, and maintain test reports, ensure adherence to standard operating procedures and regulatory guidelines, and support investigations of deviations or non-conformities. Daily responsibilities include calibrating instruments, maintaining laboratory records, collaborating with quality assurance and production teams, and contributing to continuous improvement of testing methods and quality standards. The role requires strict compliance with safety protocols and GMP practices within the laboratory environment.
Qualifications
- Strong Quality Control and Quality Assurance skills, with knowledge of GMP and regulatory requirements.
- Proficient Analytical Skills, including experience with HPLC and other relevant analytical instruments.
- Solid Laboratory Skills, including sample preparation, method execution, documentation, and instrument calibration.
- Effective Communication skills for clear reporting, documentation, and coordination with cross-functional teams.
- Minimum 1 year of experience in pharmaceutical quality control or a related laboratory role.
- Bachelor’s degree in Pharmacy, Chemistry, or a related scientific discipline.
- Attention to detail, strong organizational skills, and ability to follow standard operating procedures accurately.
- Familiarity with data integrity principles and basic computer skills for laboratory information management.
Required Skills
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