QC Job at Sava Healthcare | Pharmacy Graduates, Apply Now
SAVA Healthcare is seeking an Executive – QC for its state-of-the-art pharmaceutical manufacturing facility in Surendranagar. This QC Job at Sava Healthcare is ideal for professionals with 3–5 years of QC experience who want to ensure compliance, uphold high-quality standards, and contribute to continuous improvement in pharmaceutical manufacturing. Join one of India’s fastest-emerging pharma companies with a strong global presence.
- Job Position: Executive Quality Control
- Location: Surendranagar Plant
About the Company
SAVA Healthcare is one of India’s fastest-growing pharmaceutical companies, with a global footprint spanning Canada, Ukraine, the CIS, Asia, Latin America, Africa, and the Far East. With manufacturing plants in Surendranagar, Malur, and soon Indore, SAVA produces a wide range of dosage forms across multiple therapeutic categories. Its GMP-compliant, state-of-the-art facilities include specialized sections for tablets, oral dry powders, capsules, nasal sprays, DPIs, creams, gels, and ointments. Supported by an advanced in-house R&D center, SAVA focuses on formulation and analytical development, with an annual turnover exceeding ₹200 crore and a dedicated team of over 500 employees.
Job Description
The Executive – QC will be responsible for maintaining high-quality standards in pharmaceutical manufacturing at the Surendranagar Plant. This includes performing chemical, physical, and microbiological tests, ensuring compliance with GMP/GLP, and contributing to audits and continuous improvement initiatives.
Key Responsibilities
- Conduct routine and non-routine testing of raw materials, in-process samples, and finished products.
- Perform stability testing, validation studies, and advanced analytical work using HPLC, GC, and UV-VIS.
- Maintain accurate QC records and ensure compliance with GMP, GLP, and regulatory requirements.
- Prepare, review, and update SOPs and test methods.
- Participate in internal and external audits, inspecting raw and packaging materials.
- Investigate quality issues, deviations, and OOS results with CAPA implementation.
- Support new product development through QC expertise.
- Train junior QC staff and stay updated on industry advancements.
Qualifications
- Bachelor’s/Master’s in Chemistry, Pharmacy, Microbiology, or related field.
- 3–5 years of pharmaceutical QC experience.
- Strong knowledge of GMP, GLP, and global regulatory standards (FDA/EMA).
- Hands-on experience with analytical instruments and LIMS software.
- Excellent attention to detail, analytical, and communication skills.
Preferred Qualifications:
- Experience in method development and advanced analytical techniques.
- Certification in Quality Management Systems (ISO 9001).
- Awareness of the latest QC industry trends and best practices.
Benefits of Joining the Company
- Work in a GMP-compliant, world-class manufacturing environment.
- Exposure to global markets and international regulatory standards.
- Opportunities for professional growth and learning in pharmaceutical QC.
- Collaborative and innovation-driven work culture.
