Optimus Pharma Pvt. Ltd. is conducting a walk-in interview for experienced professionals in Quality Assurance (QA), Development Quality Assurance (DQA), In-Process Quality Assurance (IPQA), and Quality Control (QC) at its Formulations Division in Hyderabad.
This is an excellent opportunity for B.Pharm, M.Pharm, and M.Sc Chemistry graduates seeking career growth in a reputed pharmaceutical formulations company. Candidates with experience in validations, qualifications, development operations, OSD/SSD IPQA, and QC analytical testing are encouraged to attend.
Job Highlights
- Company: Optimus Pharma Pvt. Ltd. – Formulations Division
- Department: Quality Assurance & Quality Control
- Interview Date: 20 June 2026 (Saturday)
- Interview Time: 09:00 AM to 01:00 PM
- Location: Pashamylaram, Hyderabad
- Industry: Pharmaceutical Formulations
- Experience Required: 2–8 Years
Available Positions
| Department | Qualification | Experience | Key Responsibilities |
|---|---|---|---|
| QA | B.Pharm / M.Pharm | 4–6 Years | Validation and Qualification activities in formulations |
| DQA | B.Pharm / M.Pharm | 5–7 Years | Formulation development quality operations |
| IPQA | B.Pharm / M.Pharm | 2–6 Years | In-process quality assurance activities in OSD/SSD plants |
| QC | B.Pharm / M.Sc Chemistry | 3–8 Years | Raw material, packing material, stability and finished product analysis |
Key Responsibilities
Quality Assurance (QA)
- Execute validation and qualification protocols.
- Ensure compliance with GMP requirements.
- Review and approve quality documentation.
- Support audits and regulatory inspections.
Development Quality Assurance (DQA)
- Oversee formulation development quality systems.
- Ensure documentation compliance during product development.
- Support technology transfer and scale-up activities.
In-Process Quality Assurance (IPQA)
- Conduct line clearance and in-process checks.
- Monitor manufacturing operations in OSD/SSD facilities.
- Ensure adherence to SOPs and GMP standards.
Quality Control (QC)
- Perform raw material and packing material testing.
- Conduct HPLC-based analysis and stability studies.
- Manage stability chambers and finished product testing.
- Prepare analytical reports and documentation.
Eligibility Criteria
Educational Qualification
- B.Pharm
- M.Pharm
- M.Sc Chemistry (for QC roles)
Experience
- QA: 4–6 Years
- DQA: 5–7 Years
- IPQA: 2–6 Years
- QC: 3–8 Years
Preferred Skills
- GMP and regulatory compliance knowledge
- Validation and qualification expertise
- HPLC operation and troubleshooting
- Documentation and investigation handling
- OSD and SSD manufacturing exposure
Salary & Benefits
Based on current pharmaceutical industry standards, the expected salary range is:
- ₹4.5 LPA – ₹10 LPA (depending on role, experience, and interview performance)
Additional benefits may include:
- Performance-based growth opportunities
- Exposure to regulated pharmaceutical operations
- Learning and career advancement programs
- Competitive compensation package
Walk-In Interview Details
Date: Saturday, 20 June 2026
Time: 09:00 AM – 01:00 PM
Venue:
Optimus Pharma Pvt. Ltd. (Formulations)
Plot No. 73/B, Survey No. 144/Part, EPIP, Pashamylaram Village, Near Isnapur, Sangareddy, Hyderabad, Telangana
