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Company Description Nicsphere is a leading manufacturer of high-quality USP and EP grade nicotine API, operating advanced automated production facilities in Dakor, India. Candidates joining Nicsphere can expect to work in a technically driven environment focused on quality, safety, and continuous improvement.
Role Description This is a full-time, on-site QA Executive role based in Dakor. The QA Executive will oversee day-to-day quality assurance activities, including monitoring compliance with internal standards, regulatory requirements, and customer specifications. Responsibilities include reviewing and approving quality documentation, SOPs, and batch records; coordinating with production and quality control teams to investigate deviations and non-conformances; and supporting root cause analysis and corrective and preventive actions (CAPA). The role also involves performing or supporting internal quality audits, maintaining quality management systems, and contributing to continuous improvement initiatives. The QA Executive will collaborate with cross-functional teams to ensure consistent product quality, assist in training personnel on QA procedures, and prepare reports and summaries for management review.
Qualifications
- Strong foundation in Quality Control and familiarity with laboratory testing and inspection processes.
- Experience in Quality Assurance, including SOP development, documentation review, and compliance monitoring.
- Knowledge of Quality Management systems and principles, with exposure to standards such as USFDA or similar frameworks.
- Background in Quality Auditing, including participation in or coordination of internal and external audits.
- Educational background in chemical or related scientific disciplines (chemistry, chemical engineering, pharmaceuticals) is preferred.
- Understanding of regulatory and industry standards relevant to API manufacturing.
- Strong analytical and problem-solving skills, with the ability to support investigations and CAPA implementation.
- Effective communication skills and ability to work collaboratively with production, QC, and management teams.
- Attention to detail, good documentation practices, and proficiency with basic computer applications.
- Prior experience in a manufacturing environment, especially pharmaceuticals, is an advantage.
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