Quality Control Specialist

Company Description Vihita Drug & Intermediate is a pharmaceutical company focused on the development and production of drug substances and intermediates with a strong emphasis on quality, safety, and regulatory compliance. The organization is committed to maintaining robust manufacturing and testing standards to support reliable supply to its customers. Team members are encouraged to follow established processes while contributing to continuous improvement initiatives. The company offers opportunities to grow professionally within a structured, quality-driven environment.
Role Description The Quality Control Specialist is a full-time, on-site role based in Ankleshwar. This role is responsible for performing routine and non-routine testing of raw materials, intermediates, and finished products using established analytical methods. The specialist documents and reviews test results, ensures compliance with internal specifications and regulatory standards, and promptly reports deviations or nonconformities. Day-to-day responsibilities include maintaining laboratory instruments, preparing test protocols and reports, participating in stability studies, and supporting investigations and root cause analysis. The role also collaborates closely with production and quality assurance teams to ensure that products consistently meet defined quality requirements.
Qualifications
Candidates should possess strong skills in Quality Control, including sampling, testing, data recording, and documentation.
Candidates should possess skills in Quality Assurance and Quality Management to support compliance, continuous improvement, and adherence to company policies.
Candidates should possess knowledge of Good Manufacturing Practice (GMP) and Quality Auditing to ensure regulatory alignment and effective internal audits.
Relevant qualifications such as a diploma or degree in Pharmacy, Chemistry, or a related scientific discipline.
Experience in pharmaceutical or chemical manufacturing environments, particularly in QC or QA roles, is preferred.
Ability to work with laboratory instruments, follow SOPs precisely, and interpret analytical data accurately.
Strong attention to detail, problem-solving skills, and the ability to collaborate effectively with cross-functional teams.

Work arrangement
No