Optimus Pharma Pvt. Ltd., a leading pharmaceutical manufacturing company, has announced a walk-in interview drive for experienced professionals in the Formulations Division. The recruitment drive is being organized through Sekhmet Pharmaventures and offers opportunities in Quality Assurance (QA), Development Quality Assurance (DQA), In-Process Quality Assurance (IPQA), and Quality Control (QC) departments.

Candidates with relevant pharmaceutical industry experience in formulation manufacturing are encouraged to attend this walk-in interview and explore career opportunities with one of India’s growing pharmaceutical organizations.

Company Overview

Optimus Pharma Pvt. Ltd. is known for its expertise in pharmaceutical formulations and adherence to global quality standards. The company focuses on manufacturing high-quality pharmaceutical products while maintaining strict compliance with regulatory requirements and Good Manufacturing Practices (GMP).

Available Positions

1. Quality Assurance (QA)

Qualification: B.Pharm / M.Pharm

Experience: 4–6 Years

Key Responsibilities:

Validation and qualification activities

Documentation review and compliance management

Process validation for formulation products

Regulatory compliance support

2. Development Quality Assurance (DQA)

Qualification: B.Pharm / M.Pharm

Experience: 5–7 Years

Key Responsibilities:

Formulation development quality oversight

Development documentation review

Technology transfer support

Quality system implementation

3. In-Process Quality Assurance (IPQA)

Qualification: B.Pharm / M.Pharm

Experience: 2–6 Years

Key Responsibilities:

Line clearance and in-process checks

Batch manufacturing monitoring

GMP compliance verification

Process control activities in OSD/SSD plants

4. Quality Control (QC)

Qualification: B.Pharm / M.Sc (Chemistry)

Experience: 3–8 Years

Key Responsibilities:

Raw material and packing material analysis

HPLC operation and analytical testing

Stability studies

Finished product testing and documentation

Walk-In Interview Details

Interview Date: 20 June 2026 (Saturday)

Time: 09:00 AM to 01:00 PM

Venue:

Optimus Pharma Pvt. Ltd. (Formulations)

Plot No. 73/B, Survey No. 144/Part, EPIP, Pashamylaram (V), Near Isnapur, Sangareddy, Hyderabad, Telangana.

Why Join Optimus Pharma?

Opportunities in a growing formulations business

Exposure to regulated pharmaceutical manufacturing

Strong quality-driven work culture

Career growth in QA, QC, and compliance functions

Hands-on experience with advanced pharmaceutical processes

Documents to Carry

Candidates attending the interview should bring:

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slips

Government Photo ID Proof

Passport Size Photographs

Technical FAQs

1. What is the role of validation in pharmaceutical Quality Assurance?

Validation ensures that manufacturing processes, equipment, and systems consistently produce products meeting predetermined quality standards. It is a key regulatory requirement under GMP guidelines.

2. What are the major responsibilities of IPQA during manufacturing?

IPQA professionals perform line clearance, monitor critical process parameters, verify GMP compliance, conduct in-process checks, and ensure batch documentation accuracy throughout production.

3. Why is HPLC important in Quality Control laboratories?

High-Performance Liquid Chromatography (HPLC) is used for identification, assay determination, impurity profiling, and stability testing of pharmaceutical products with high accuracy and precision.

4. What is the purpose of stability studies in pharmaceuticals?

Stability studies evaluate how a drug product maintains its quality, safety, and efficacy over time under different environmental conditions, helping establish shelf life and storage conditions.

5. What is the difference between QA and QC in the pharmaceutical industry?

QA focuses on process compliance, documentation, validation, and quality systems to prevent defects, while QC focuses on testing raw materials, in-process samples, and finished products to detect defects and ensure product quality.