Quality Assurance Sampling Executive

Company Description Pharmaceuticals Company Goa is a growing pharmaceutical manufacturer focused on producing safe, high-quality medications for domestic and international markets. The organization is committed to strict regulatory compliance and continuous improvement across all production and quality functions. Team members work in a collaborative environment with modern facilities and standardized procedures. The company values integrity, scientific rigor, and a strong focus on patient safety, offering opportunities for professional development in quality-focused roles.
Role Description The Quality Assurance Sampling Executive is a full-time, on-site role based in Goa, India. This position is responsible for systematic sampling of raw materials, in-process materials, and finished products in accordance with established standard operating procedures and regulatory guidelines. Daily tasks include coordinating with production and QC teams, labeling and documenting samples, maintaining sampling records and logs, and supporting investigations related to deviations or nonconformities. The role involves verifying adherence to quality standards on the shop floor, assisting in internal audits, and contributing to continuous improvement initiatives. The executive will also help ensure that all sampling activities comply with Good Manufacturing Practices (GMP) and internal quality policies.
Qualifications
Demonstrated skills in Quality Control and Quality Assurance for pharmaceutical or related manufacturing environments.
Experience or knowledge in Quality Management and Quality Auditing to support compliance with GMP and regulatory requirements.
Background in Food Technology or related scientific disciplines, with the ability to apply technical knowledge to sampling and testing processes.
Degree or diploma in Pharmacy, Pharmaceutical Sciences, Chemistry, Food Technology, or a related field.
Strong attention to detail, documentation accuracy, and familiarity with GMP and regulatory guidelines (e.g., WHO, FDA, or similar).
Ability to work on-site in a manufacturing environment, collaborate with cross-functional teams, and follow standardized procedures.
Basic computer skills for data entry, report preparation, and use of quality management systems; prior experience in pharmaceuticals is an advantage.

Work arrangement
No