Looking for QA jobs or QC jobs in Hyderabad? Sekhmet Pharmaventures (Optimus Group) is conducting a Walk-in Interview on 18 April 2026 for Quality Assurance (Executive/Senior Executive) and Quality Control (Executive/Senior Executive) positions. Candidates with 3–8 years of experience in API Manufacturing or Formulation are invited to attend.
Contents
About the Company
Sekhmet Pharmaventures is part of the Optimus Group and operates under brands such as Anjan Drug Private Limited (ADPL) and Bulk Drugs. The company is engaged in the manufacturing of high-quality Active Pharmaceutical Ingredients (API) and Formulations.
With multiple manufacturing units across Telangana and Chennai, Sekhmet Pharmaventures focuses on quality, regulatory compliance, and continuous expansion in the pharmaceutical sector.
Job Details
- Company Name: Sekhmet Pharmaventures (Optimus Group)
- Positions:
- Quality Assurance (Executive / Senior Executive)
- Quality Control (Executive / Senior Executive)
- Qualification: B.Sc / B.Pharm / M.Sc / M.Pharm
- Experience: 3–8 years in QA/QC (API Manufacturing or Formulation)
- Plant Locations:
- Dothigudem (Unit 1)
- Ramalingampally (Unit 3)
- Pashamylaram (Unit 4)
- Chennai (Unit 5 & 6)
- Walk-in Date: 18 April 2026 (Saturday)
- Time: 8:30 AM – 3:00 PM
Job Description
Sekhmet Pharmaventures is expanding its Quality team and looking for experienced professionals to strengthen QA and QC functions across its API and Formulation manufacturing units. The roles involve ensuring compliance with cGMP, regulatory standards, and maintaining product quality throughout the manufacturing process.
Skills/Qualifications
- B.Sc / B.Pharm / M.Sc / M.Pharm qualification
- 3–8 years of hands-on experience in Quality Assurance or Quality Control
- Experience in API Manufacturing or Formulation is mandatory
- Strong knowledge of cGMP, GLP, SOPs, and regulatory requirements
- Proficiency in analytical instruments (for QC role)
- Good documentation practices and investigation skills
- Ability to work effectively in a team environment
Key Responsibilities
- Execute and monitor Quality Assurance / Quality Control activities
- Perform in-process checks, finished product analysis, and stability studies (QC)
- Conduct audits, investigations, CAPA, and change control (QA)
- Ensure compliance with cGMP and other regulatory guidelines
- Review batch manufacturing records, analytical data, and documentation
- Support regulatory inspections and audits
- Maintain laboratory standards and equipment calibration (QC)
Benefits/Perks
- Opportunity to work with a growing pharmaceutical group
- Exposure to API and Formulation manufacturing
- Career growth in Quality functions
- Professional work environment with modern facilities
- Multiple plant locations to choose from
How to Apply
Walk-in Interview Details
- Date: 18 April 2026 (Saturday)
- Time: 8:30 AM – 3:00 PM
- Venue: Vashishta Banquets, Plot No. 11, Surya Nagar Main Road, Above IDFC First Bank, Opp. Royal Enfield Showroom, Chinthal, Quthbullapur, Hyderabad, Telangana 500037
Email for Queries: careers@sekhmetpharma.com
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Sekhmet LinkedIn page.

Candidates are requested to carry their updated resume, educational certificates, experience letters, and Aadhaar/PAN.
For more QA jobs, QC jobs, API jobs in Hyderabad, and pharmaceutical opportunities across India, visit Pharma Recruiter.
Don’t miss this opportunity — attend the walk-in on 18 April 2026!
Why You Should Join Sekhmet Pharmaventures
Sekhmet Pharmaventures offers a stable and growth-oriented platform for Quality professionals. With multiple manufacturing units and a focus on quality and compliance, the company provides excellent learning opportunities and long-term career prospects in the pharmaceutical industry.
FAQs
What is the walk-in interview date and venue?
The walk-in is on 18 April 2026 from 8:30 AM to 3:00 PM at Vashishta Banquets, Chinthal, Quthbullapur, Hyderabad.
Which qualifications are required?
B.Sc / B.Pharm / M.Sc / M.Pharm with 3–8 years of QA/QC experience in API or Formulation.
Which plant locations are available?
Positions are open at Dothigudem, Ramalingampally, Pashamylaram (Telangana), and Chennai units.
Is experience in API mandatory?
Yes, QA/QC experience in API Manufacturing or Formulation is required.
Can I send my resume by email?
You can email your resume to careers@sekhmetpharma.com, but attending the walk-in is recommended.