ANEETA
Website:
girnargroup.com
Job details:
Company Description Aneeta Group of companies is a certified manufacturer of pharmaceutical primary and secondary packaging products, operating under ISO 9001, ISO 14001, ISO 13485, ISO 15378, and DMF standards. The company adheres to cGMP, ISO, and other global regulations, supported by advanced infrastructure and sophisticated equipment. All products are produced in dedicated production blocks with exclusive DMF, ensuring traceability and compliance. An in-house R&D and tool room enable customized solutions, consistent quality, and reliable production. Aneeta Group of Companies portfolio includes seals, droppers, measuring devices, cans, ophthalmic bottles, syringes, vials, tubes, laminates, and other specialized packaging components for the pharmaceutical sector.
Role Description The QA/QC Manager is a full-time, on-site role based in Gandhinagar, Gujarat responsible for overseeing quality assurance and quality control activities across all packaging products and processes. This role includes establishing, implementing, and monitoring quality systems aligned with ISO, cGMP, and DMF requirements, as well as managing documentation, SOPs, and audit readiness. The QA/QC Manager will lead inspection and testing of raw materials, in-process components, and finished goods, investigate non-conformities, and drive corrective and preventive actions. Daily tasks involve coordinating with production, R&D, and regulatory teams to ensure product compliance, maintaining calibration and validation records, and training staff on quality standards. The role also includes supporting customer audits, handling change controls, and continuously improving processes to enhance reliability, safety, and customer satisfaction.
Qualifications
- Strong knowledge of pharmaceutical packaging quality systems, including ISO 9001, ISO 13485, ISO 15378, cGMP, and DMF compliance.
- Experience in QA/QC methodologies such as inspection planning, sampling, testing protocols, validation, and CAPA management.
- Proficiency in quality documentation, including SOPs, batch records, deviation reports, change controls, and audit documentation.
- Familiarity with packaging materials and processes (e.g., seals, blisters, bottles, syringes, tubes, laminates, and sterilization-related products).
- Ability to lead and mentor QA/QC teams, conduct training, and collaborate effectively with production, R&D, and regulatory functions.
- Strong analytical and problem-solving skills, with attention to detail and a focus on continuous improvement.
- Bachelor’s or Master’s degree in Pharmacy, Engineering, Science, or a related field, with prior experience in pharmaceutical or medical device packaging preferred.
- Comfort working on-site in a manufacturing environment, with readiness to support internal and external audits and regulatory inspections.
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