U.S. Pharmacopeia Hiring Quality Assurance Specialist
- Opportunity for QA Specialists with MSc Chemistry or Pharmacy Background – Hyderabad Location
- Position Overview
- Key Responsibilities
- H3: Quality Systems & Process Audits
- Supplier Quality Management
- Document & Data Review
- Investigations and CAPA Implementation
- Required Educational Background
- Experience & Skills Required
- About USP
- Â How to Apply
- Quick Summary Table
Quality Assurance Specialist Jobs in Hyderabad | Hiring MSc Chemistry, MSc Pharmacy Professionals
Apply now for QA Specialist job in Hyderabad at USP. Open for MSc Chemistry, MSc Pharmacy graduates with 8-10 years experience. Full-time opportunity.
Opportunity for QA Specialists with MSc Chemistry or Pharmacy Background – Hyderabad Location
The U.S. Pharmacopeial Convention (USP) is actively hiring for the position of Quality Assurance Specialist at its Hyderabad location. This full-time opportunity is ideal for professionals with an MSc in Chemistry, Pharmacy, or related life sciences and a strong foundation in quality assurance processes within the pharmaceutical or analytical industry.
This role offers a dynamic, inclusive work environment and the chance to contribute to a globally respected organization setting quality standards for health products.
Position Overview
Job Title: Quality Assurance Specialist
Job Location: Hyderabad, India
Job Type: Full-Time
Department: Quality Assurance
Req ID: QUALI002667
As a QA Specialist, you will review reference standards qualification records, conduct internal audits, and support continuous quality system improvements. The position requires a hands-on approach, contributing to supplier evaluations and resolution of non-conformities while maintaining ISO and GMP compliance.
Key Responsibilities
H3: Quality Systems & Process Audits
- Support and implement quality programs and SOPs.
- Review and approve IQ/OQ/PQ, calibration, and batch record documents.
- Lead internal process audits and ensure ISO 9001/17025 adherence.
Supplier Quality Management
- Conduct supplier evaluations and performance audits.
- Manage supplier-related investigations and CAPAs.
Document & Data Review
- Review method validation reports, technical documents, and analytical data.
- Ensure compliance with quality standards for reference and analytical materials.
Investigations and CAPA Implementation
- Evaluate deviations, quality complaints, and recommend corrective/preventive actions.
- Support resolution and closure of quality incidents.
Required Educational Background
Candidates must have a:
- Master’s degree in Chemistry, Pharmacy, or Biology
- Additional preference for individuals with analytical method validation and laboratory equipment experience.
Experience & Skills Required
- 8–10 years of industry experience in Quality Assurance roles.
- At least 3 years hands-on experience in analytical lab environments.
- Strong understanding of ISO 9001, ISO 17025, and GMP regulations.
- Effective communication and leadership skills.
- Familiarity with MS Office (Word, Excel, PowerPoint).
About USP
The U.S. Pharmacopeial Convention is a global, nonprofit organization working with leading scientific minds to improve public health standards for medicines and dietary supplements. Headquartered in the U.S. and with operations in over 20 countries, USP champions equity, transparency, and global quality assurance.
 How to Apply
👉 Interested candidates can apply directly via the USP careers page:
Apply Here
Quick Summary Table
| Company Name | Current Vacancies | Required Education | Experience Required |
|---|---|---|---|
| USP (U.S. Pharmacopeial Convention) | Quality Assurance | MSc Chemistry, MSc Pharmacy | 8–10 years in QA, 3+ years in lab operations |
To apply for this job please visit usp.jobs.