Company Description Globela Pharma Private Limited is a reputed pharmaceutical company based in Surat, Gujarat, India, with a manufacturing unit in the Sachin G.I.D.C. industrial area. The company operates state-of-the-art, WHO-GMP approved facilities dedicated to producing high-quality general and oncology (anti-cancer) pharmaceutical products.

Its manufacturing units are certified by multiple international regulatory authorities, including those in Myanmar, Sri Lanka, Vietnam, Cambodia, Nigeria, Kenya, and Tanzania. Operations are led by skilled and experienced professionals across Production, Quality Control, Quality Assurance, and R&D; under the guidance of top management.

Globela

Pharma is expanding its generic product range and is committed to achieving strong growth through quality, innovation, and support from its stakeholders.

Role Description This is a full-time, on-site QA/QC role based at the manufacturing facility in Surat. The role involves routine quality testing of raw materials, in-process samples, and finished products, ensuring compliance with internal standards and regulatory requirements.

The QA/QC professional will review and maintain documentation, including batch records, standard operating procedures, and deviations, while supporting change control and CAPA activities. Daily responsibilities include monitoring adherence to WHO-GMP guidelines on the shop floor, participating in internal audits,



and assisting in qualification and validation processes. The role also collaborates closely with Production and R&D; teams to resolve quality issues, support continuous improvement initiatives, and maintain a strong culture of quality and safety.

Qualifications

- Strong foundation in Quality Control, including routine testing, data recording, and laboratory practices.
- Experience in Quality Assurance activities such as documentation control, deviation management, and CAPA implementation.
- Knowledge of Quality Management principles, including risk-based thinking and continuous improvement methodologies.
- Hands-on understanding of Valuable Manufacturing Practice (GMP) and WHO-GMP requirements in a pharmaceutical environment.
- Exposure to Quality Auditing, including participation in internal audits and support during regulatory or customer audits.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Pharmaceutical Science, or a related discipline.
- Familiarity with analytical instruments and basic statistical analysis of test results.
- Strong attention to detail, documentation skills, and ability to work systematically in a regulated environment.
- Effective communication and collaboration skills for working with cross-functional teams.
- Prior experience in oncology or generic pharmaceutical manufacturing is an advantage.

📌 QA/QC (Surat)
🏢 Globela Pharma Private
📍 Surat