CIRO Pharma Private Limited has announced a walk-in recruitment drive for experienced professionals in Quality Control, Microbiology, Production, Warehouse, and Engineering Stores departments. Candidates with relevant pharmaceutical industry experience are invited to attend the walk-in interview at the company’s manufacturing facility in Telangana.
If you are looking for pharmaceutical jobs in Quality Control, Production, or Microbiology, this recruitment drive offers multiple opportunities across different functions.
Job Overview
Company Name: CIRO Pharma Private Limited
Job Type: Walk-In Interview
Walk-In Date: 19 July 2025 (Sunday)
Interview Time: 10:00 AM
Job Location: Siddipet, Telangana, India
Preferred Candidates: Immediate Joiners, Male Candidates, and Relocating Individuals
Available Positions
| Department | Position | Experience | Vacancies |
|---|---|---|---|
| Quality Control | Analyst | 5 Years | 15 |
| Quality Control | Chromatographic Reviewer | 7 Years | 2 |
| Quality Control | Method Validation Reviewer | 7 Years | 2 |
| Quality Control | GLP Coordinator | 5 Years | 2 |
| Microbiology | Document Reviewer | 8 Years | 2 |
| Microbiology | Junior Executive | 3 Years | 5 |
| Microbiology | Junior Executive (Culture & Media Management) | 3 Years | 5 |
| Microbiology | Executive | 3 Years | 5 |
| Microbiology | Executive (BET/Sterility) | 5 Years | 2 |
| Production | Junior Executive (Granulation, Compression, Coating & Capsule Filling) | 5 Years | 5 |
| Production | Junior Executive (Bottle & Blister Packing) | 5 Years | 5 |
| Warehouse | Executive | 5 Years | 5 |
| Engineering Stores | Executive | 5 Years | 2 |
Roles & Responsibilities
Depending on the position, selected candidates will be responsible for:
- Perform HPLC, GC, UV, IR, TLC, KF, Potentiometry and Wet Analysis.
- Conduct raw material, packing material and water sample testing.
- Execute calibration, preventive maintenance and qualification activities.
- Review chromatographic data, audit trails and analytical reports.
- Handle Analytical Method Validation (AMV) documentation and review.
- Coordinate with vendors and third-party laboratories.
- Review microbiology documents and perform MLT, BET and sterility validation.
- Conduct environmental monitoring of aseptic areas.
- Manage microbiological cultures and media.
- Perform water, product and microbial limit testing.
- Execute granulation, compression, coating and capsule filling operations.
- Operate bottle packing, CVC and blister packing lines.
- Handle isolator dispensing, cleaning and warehouse operations.
- Manage engineering stores, project materials and laboratory consumables.
Required Qualifications
The official notification highlights experience requirements for each role. Relevant qualifications generally applicable to these positions include:
- B.Pharm
- M.Pharm
- B.Sc.
- M.Sc.
- Diploma
- B.Tech / B.E.
- ITI (for relevant technical roles)
Candidates should possess relevant pharmaceutical manufacturing experience as specified for the respective role.
Experience Required
- 3 Years
- 5 Years
- 7 Years
- 8 Years
Experience requirement varies according to the position applied for.
Salary & Benefits
Salary is expected to be offered based on qualification, experience and company standards.
Typical expected salary range:
- โน3.5 LPA โ โน10 LPA (depending on role and experience)
Additional benefits may include:
- Competitive compensation
- Career growth opportunities
- Professional work environment
- Learning and development opportunities
Walk-In Venue
CIRO Pharma Private Limited
Plot No. 28, Biotech Park Phase III,
Karakapatla, Markook Mandal,
Siddipet, Telangana
Documents to Carry
Candidates should carry:
- Updated Resume
- Recent Passport Size Photographs
- Educational Certificates
- Experience Certificates
- Latest Salary Documents (if applicable)
- Government Photo ID Proof
How to Apply
Eligible candidates can directly attend the walk-in interview on the scheduled date and time with all required original documents and photocopies.
Candidates are advised to reach the venue before the reporting time to complete the registration process smoothly.
