Quality Control Job at Sava Healthcare | Apply Now for the Executive Position
A leading regulated pharmaceutical plant in Indore is seeking a QC Executive to join its Quality Control department. This Quality Control Job is designed for professionals with 2–5 years of experience and a background in B.Pharm, M.Pharm, or M.Sc. The executive will be responsible for the analysis of Raw Materials (RM), Finished Goods (FG), and Stability samples, as well as executing Analytical Method Validations (AMV) and Microbiological testing. Candidates must demonstrate strong expertise in cGMP/GLP and the operation of high-end instruments like HPLC and GC for this Pharma Job
- Job Title: QC Executive – (RM / FG / Stability / AMV & PV / Microbiology)
- Location: Indore – Regulated Pharma Manufacturing Plant
About the Company
Sava Healthcare is a Regulated Pharma Manufacturing Plant located in Indore, committed to upholding the highest standards of global pharmaceutical excellence. The facility operates in strict compliance with international regulatory bodies, including the USFDA, EU-GMP, and WHO. By integrating advanced analytical technologies with a robust Quality Management System (QMS), the company ensures that every product manufactured meets stringent safety, efficacy, and purity profiles before reaching patients worldwide.
Quality Control Job Purpose
To perform quality control testing and analysis of raw materials, finished products, stability samples, and microbiological parameters as per current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), pharmacopeial standards, and regulatory requirements to ensure product quality and compliance.
Key Responsibilities of the Pharma Job
1. Testing and Analysis
- Perform chemical and instrumental testing of Raw Materials (RM) and Finished Goods (FG) as per pharmacopeial and in-house specifications.
- Conduct Stability Studies in line with ICH guidelines and maintain records of stability trends.
- Execute Analytical Method Validations (AMV) and support Process Validation (PV) testing.
- Carry out Microbiological analysis of samples, including environmental monitoring, water testing, and microbial limit tests.
2. Documentation and Compliance
- Maintain accurate, complete, and timely documentation (analytical reports, logbooks, LIMS/ERP entries).
- Ensure compliance with cGMP, GLP, and regulatory standards (USFDA, EU-GMP, WHO, etc.).
- Participate in internal audits, external regulatory inspections, and implement CAPAs.
- Prepare and review standard operating procedures (SOPs), specifications, and testing protocols.
3. Equipment Operation & Calibration
- Operate and calibrate instruments like HPLC, GC, UV, IR, Dissolution Apparatus, FTIR, etc.
- Ensure timely preventive maintenance and validation of QC instruments.
4. Cross-functional Coordination
- Coordinate with Production, QA, Regulatory Affairs, and other relevant departments to resolve testing issues and support product release timelines.
- Participate in investigations of OOS/OOT results, deviations, and change controls.
Key Skills & Competencies
- Sound knowledge of cGMP/GLP and ICH guidelines.
- Hands-on experience with analytical instruments and microbiology techniques.
- Strong documentation and data integrity practices.
- Good communication and team collaboration skills.
- Eye for detail and high level of integrity.
Educational Qualifications
- B.Pharm / M.Pharm / M.Sc. (Pharmaceutical Sciences)
Experience Required for the Quality Control Job
- 2–5 years of relevant experience in a regulated pharmaceutical manufacturing environment.
Preferred Certifications
- Training in Data Integrity, cGMP, QMS, or Instrument Handling is an advantage.
