L 5 - NDDS/TT
savaglobal
Executive/Sr. Executive - Quality Assurance (IPQA)
savaglobal· QA - IPQA - (Surendranagar)
About this role
Job Title: Executive - Quality Assurance
Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories.
Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations.
Job Location: Surendranagar Plant
Job Summary:
We are seeking a dedicated and detail-oriented Quality Assurance (QA) Personnel to join our Pharma Manufacturing Plant. The ideal candidate will be responsible for ensuring that our manufacturing processes comply with regulatory standards and internal quality protocols. This role is critical in maintaining product quality, safety, and efficacy, and ensuring our products meet all required specifications before reaching the market.
Key Responsibilities
Quality Management System (QMS):
- Maintain and enhance the Quality Management System (QMS) to ensure compliance with GMP (Good Manufacturing Practices) and other regulatory requirements.
- Develop, review, and update quality assurance policies, procedures, and SOPs.
Documentation and Records:
- Ensure all quality-related documentation is accurate, complete, and maintained according to regulatory standards.
- Review and approve batch records, quality control reports, and other manufacturing documentation.
Compliance and Audits:
- Conduct internal audits and support external audits to ensure compliance with regulatory requirements and company standards.
- Prepare audit reports, identify non-conformances, and implement corrective and preventive actions (CAPAs).
Product Quality Assurance:
- Monitor and verify the quality of raw materials, in-process materials, and finished products through regular inspections and testing.
- Investigate and resolve quality issues, deviations, and complaints related to manufacturing processes and products.
Process Validation and Improvement:
- Participate in process validation activities to ensure manufacturing processes are robust and reproducible.
- Identify areas for process improvement and implement quality enhancement initiatives.
Training and Development:
- Provide training and guidance to manufacturing staff on quality assurance practices, GMP, and regulatory requirements.
- Stay updated on the latest industry trends, regulations, and best practices in quality assurance.
Risk Management:
- Conduct risk assessments to identify potential quality issues and implement strategies to mitigate risks.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
Qualifications
Education:
- Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related field. Advanced degree or professional certification (e.g., Certified Quality Auditor) is a plus.
Experience:
- Minimum of 3-5 years of experience in quality assurance within the pharmaceutical manufacturing industry.
- Strong understanding of GMP, regulatory requirements (e.g., FDA, EMA), and quality management systems.
Skills:
- Excellent analytical, problem-solving, and decision-making skills.
- Strong attention to detail and organizational skills.
- Effective communication and interpersonal skills.
- Proficiency in using quality management software and MS Office Suite (Word, Excel, PowerPoint).
Personal Attributes:
- High level of integrity and commitment to maintaining quality standards.
- Ability to work independently and collaboratively in a team-oriented environment.
- Proactive and results-oriented with a focus on continuous improvement.
Frequently Asked Questions
Is the salary disclosed for the Executive/Sr. Executive - Quality Assurance (IPQA) position at savaglobal?
The salary for this Executive/Sr. Executive - Quality Assurance (IPQA) role at savaglobal is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Executive/Sr. Executive - Quality Assurance (IPQA) position at savaglobal located?
This Executive/Sr. Executive - Quality Assurance (IPQA) role at savaglobal is based in Surendranagar, GJ, India. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Executive/Sr. Executive - Quality Assurance (IPQA) role at savaglobal full-time or part-time?
This is listed as a FULL TIME position. It is posted as a Executive/Sr. Executive - Quality Assurance (IPQA) role in the QA - IPQA - (Surendranagar) department at savaglobal.
Which team or department does the Executive/Sr. Executive - Quality Assurance (IPQA) at savaglobal belong to?
This Executive/Sr. Executive - Quality Assurance (IPQA) position is part of the QA - IPQA - (Surendranagar) department at savaglobal. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Executive/Sr. Executive - Quality Assurance (IPQA) position at savaglobal?
Click the "Apply Now" button on this page. You will be redirected to savaglobal's official application portal hosted on keka where you can submit your application directly.
When was the Executive/Sr. Executive - Quality Assurance (IPQA) job at savaglobal posted?
This Executive/Sr. Executive - Quality Assurance (IPQA) position at savaglobal was posted on Jul 12, 2026. Apply as soon as possible — early applications are often reviewed first.
Executive/Sr. Executive - Quality Assurance (IPQA)
savaglobal
You'll be redirected to savaglobal's official application page on keka.