Pharmaceutical professionals seeking growth in a GMP-compliant environment will find an exciting opportunity at Stanford Laboratories Pvt. Ltd. The company, a WHO-GMP certified manufacturer of formulations, is hiring a QA/QC Executive for its facility in Una, Himachal Pradesh. This on-site, full-time position suits candidates passionate about quality assurance and control in the pharma sector.
With a focus on compliance, testing, and continuous improvement, this role offers hands-on involvement in maintaining high-quality standards for pharmaceutical products.
Key Responsibilities
The QA/QC Executive will handle critical functions across Quality Assurance and Quality Control departments:
Quality Assurance (QA):
- Ensure full compliance with GMP, GLP, ISO standards, and all relevant regulatory guidelines
- Prepare, review, and manage SOPs, protocols, formats, and associated records
- Support and participate in internal audits, external audits, and regulatory inspections
- Manage deviations, change controls, CAPA implementation, and risk assessment activities
- Monitor and implement quality management systems effectively
- Review batch manufacturing records, analytical reports, and other quality-related documentation
- Conduct training sessions for staff on quality procedures and regulatory compliance
Quality Control (QC):
- Perform or supervise testing of raw materials, in-process samples, and finished pharmaceutical products
- Adhere strictly to approved testing methods, specifications, and protocols
- Review and approve test results, Certificates of Analysis (COAs), and lab records
- Investigate Out of Specification (OOS), Out of Trend (OOT) results, and other non-conformances
- Oversee calibration, maintenance, and qualification of laboratory equipment and instruments
- Maintain laboratory safety protocols and ensure proper housekeeping standards
Required Qualifications and Experience
- Educational Background: B.Pharm, B.Sc., M.Pharm, or M.Sc. in relevant disciplines (Pharmaceutical Chemistry, Quality Assurance, or related fields preferred)
- Experience: 1–5 years in QA/QC roles within the pharmaceutical industry
- Strong knowledge of GMP/GLP guidelines and regulatory requirements
- Excellent documentation, analytical, and problem-solving skills
- Ability to work in a fast-paced, on-site manufacturing environment
Salary and Benefits The company offers a competitive salary package commensurate with experience and industry standards, typically in the range of ₹3.5 LPA to ₹6 LPA for this level (based on similar pharma roles in Himachal Pradesh). Additional benefits may include performance incentives, health coverage, and professional development opportunities in a supportive work culture.
How to Apply Interested and eligible candidates can share their updated CV directly with the hiring team at: anu.singh@stanlabs.com
