Join Sekhmet Pharmaventures (Optimus Drugs Unit-3) – Walk-In Interviews for Production and Quality Control Professionals
Summary: Sekhmet Pharmaventures (Optimus Drugs Unit-3), a USFDA, EU-GMP & WHO-approved API manufacturing facility in Hyderabad, is seeking talented and motivated individuals to join our Production and Quality Control teams. We are holding walk-in interviews from December 2nd, 2025, to December 13th, 2025, for the positions of Production Executive, Quality Control Executive, QC Microbiology Executive, and Senior Executive. This is an exceptional opportunity to contribute to a rapidly growing organization and advance your career in a dynamic and regulated environment. If you have 1-3 years of experience in API/Bulk Drug manufacturing and are looking for immediate joining, we encourage you to attend our walk-in interview.
About Sekhmet Pharmaventures (Optimus Drugs Unit-3):
We are a leading API (Active Pharmaceutical Ingredient) manufacturing facility committed to producing high-quality pharmaceutical products that meet global regulatory standards. Our state-of-the-art facility in Ramlingampally, Hyderabad, is approved by USFDA, EU-GMP, and WHO, reflecting our dedication to excellence in manufacturing and quality assurance. We offer a supportive and challenging work environment with opportunities for professional growth and development.
We are Hiring:
We are currently seeking qualified candidates for the following positions:
- Production Executive
- Quality Control Executive
- QC Microbiology Executive
- Senior Executive
Key Responsibilities:
The specific responsibilities for each role will vary depending on the position. However, general responsibilities include:
- Operating API production equipment (reactors, centrifuges, dryers, etc.) according to batch manufacturing records.
- Performing in-process sampling, testing, and documentation (BMR/BPR).
- Conducting chemical analysis using HPLC, GC, UV, IR, and wet chemistry methods (QC).
- Executing microbial limit tests, BET, sterility, environmental monitoring, and water analysis (QC Microbiology).
- Ensuring strict adherence to cGMP, safety protocols, and data integrity guidelines.
- Handling deviations, investigations, CAPA (Corrective and Preventive Action), and change controls.
- Coordinating with QA (Quality Assurance), production, and engineering teams.
Eligibility Criteria & Qualifications:
- Education:
- B.Pharm / M.Pharm
- B.Sc / M.Sc Chemistry
- B.Tech Chemical Engineering / Chemistry
- Experience: 1 to 3 years of relevant experience in API/Bulk Drug manufacturing.
- Knowledge: Strong understanding of cGMP (current Good Manufacturing Practices), GLP (Good Laboratory Practices), 21 CFR, and ICH guidelines.
- Availability: Immediate joiners are highly preferred.
- Preferred: Candidates with exposure to regulated markets (USFDA/MHRA) will be given preference.
Salary & Benefits:
We offer a competitive compensation package and benefits, including:
- Expected CTC: ₹3.6 – ₹6.5 LPA (based on experience & interview performance)
- Free transport & subsidized canteen
- Group mediclaim & personal accident insurance
- Provident Fund, gratuity & annual bonus
- Fast-track growth opportunities within a rapidly expanding organization.
Walk-In Interview Schedule:
- Dates: December 2nd, 2025 – December 13th, 2025
- Time: 9:00 AM to 3:00 PM
- Venue: Optimus Drugs Unit-3, Ramlingampally, Hyderabad
Important Information:
- No online applications will be accepted. Only candidates attending the walk-in interviews will be considered.
- Please bring the following documents to the interview:
- Updated resume
- Recent passport-size photograph
- Copies of educational & experience certificates
- Latest salary slip / increment letter
Confirmation:
To confirm your attendance, please email your preferred date and resume to [email protected].
We look forward to meeting you!