Senior Executive Quality Assurance

Company Description Noronic Pharmaceutical Pvt Ltd is a growing pharmaceutical organization committed to delivering safe, effective, and high-quality medicines to improve patient health outcomes. The company focuses on stringent quality standards, regulatory compliance, and continuous improvement across its manufacturing and distribution processes. With a collaborative work environment, Noronic Pharmaceutical encourages innovation, professional development, and ethical practices in all operations. Team members have the opportunity to contribute to systems and products that support healthcare providers and patients. The organization values accountability, transparency, and long-term career growth for its workforce.
Role Description The Senior Executive Quality Assurance will oversee day-to-day quality assurance activities to ensure compliance with applicable regulatory guidelines, internal SOPs, and industry standards. This full-time, on-site role in Ahmedabad includes monitoring batch manufacturing and packaging records, conducting in-process checks, and reviewing documentation for accuracy and completeness. The Senior Executive will coordinate change control, deviation handling, CAPA implementation, and investigation of quality issues, while supporting internal and external audits. The role involves collaboration with production, QC, regulatory, and other cross-functional teams to maintain GMP compliance and drive continuous improvement initiatives. The position also requires training team members on quality procedures, preparing quality reports, and supporting qualification and validation activities as needed. Also they had to prepare BMR/BPR/stability /process validation /coa /moa
Qualifications
Candidates should possess strong knowledge of pharmaceutical Quality Assurance, including GMP, GLP, and relevant regulatory guidelines (e.g., WHO, FDA, EMA as applicable).
Candidates should possess experience in document control, batch record review, SOP preparation, and effective handling of deviations, change controls, and CAPA.
Candidates should possess skills in audit preparation and participation, internal quality audits, and coordination with regulatory and compliance teams.
Candidates should possess familiarity with validation and qualification processes (equipment, utilities, processes) and basic understanding of risk assessment in quality systems.
Candidates should possess strong analytical, problem-solving, and decision-making skills, with attention to detail and a focus on accuracy.
Candidates should possess effective communication and collaboration skills to work with cross-functional teams and support training on quality procedures.
Beneficial qualifications include a bachelor’s or master’s degree in Pharmacy, Chemistry, or a related scientific discipline, and prior experience in a similar QA role within the pharmaceutical industry.
Beneficial attributes include proficiency with standard QA software tools, comfort with documentation in digital systems, and the ability to manage multiple tasks in a fast-paced environment.

Work arrangement
No