Ciron Drugs & Pharmaceuticals Pvt. Ltd., a US FDA and WHO-GMP certified leader, is hosting a walk-in drive on June 28–29, 2025, in Tarapur, Maharashtra. Join our innovative team at our advanced facility.
Contents
- 1 Event Details
- 2 About Ciron Drugs
- 3 Open Positions
- 3.1 Engineering Department
- 3.2 Microbiology Department
- 3.3 Production Department
- 3.3.1 Packing Officer (5 Vacancies)
- 3.3.2 QMS Officer/Sr. Officer (2 Vacancies)
- 3.3.3 Batch Manufacturing Operator (2 Vacancies)
- 3.3.4 Washing (Ampoule/Vial) Operator (2 Vacancies)
- 3.3.5 Eye Drops/Vial/Ampoule Filling Operator (4 Vacancies)
- 3.3.6 Autoclave/LYO Operator (4 Vacancies)
- 3.3.7 Garment Washing Operator (2 Vacancies)
- 3.3.8 Liquid Injection/Packing Sr. Officer/Executive (3 Vacancies)
- 3.4 Quality Assurance (QA) Department
- 3.5 Quality Control (QC) Department
- 3.6 Warehouse Department
- 4 Why These Roles Matter
- 5 Benefits of Joining Ciron Drugs
- 6 How to Apply
- 7 About Our Facility
- 8 Join Our Mission
Event Details
- Date: Saturday & Sunday, June 28–29, 2025
- Time: 10:00 AM to 2:00 PM
- Venue: Unit 1, N-118, N-119 & N-113, M.I.D.C., Tarapur, Boisar, Dist. Palghar – 401506, Maharashtra
- Contact: Email CV to hrd@cironpharma.com or call 8010319276 / 9607989878 / 9168040418 / 8956866757
Requirements: Bring updated CV, 1 photograph, Aadhar & PAN card, last two months’ salary slips, and CTC structure.
About Ciron Drugs
Founded in 1990, Ciron Drugs is a Mumbai-based pharmaceutical leader specializing in injectables, eye drops, and tablets. Our US FDA-approved Tarapur facility ensures global quality standards.
Why Join Us?
Work in a cGMP-compliant environment with cutting-edge technology. Enjoy competitive benefits, career growth, and the opportunity to contribute to global healthcare with a trusted brand.
Open Positions
We’re hiring for roles in Engineering, Microbiology, Production, Quality Assurance (QA), Quality Control (QC), and Warehouse. Below are the details:
Engineering Department
Plant Maintenance Officer/Sr. Officer (2 Vacancies)
- Qualification: B.E./B.Tech Mechanical or Diploma Mechanical
- Experience: 2–4 years
- Responsibilities: Maintain plant equipment, ensure cGMP compliance, and support operational efficiency.
- Skills: Expertise in mechanical maintenance, troubleshooting, and regulatory standards.
Water System Operator (5 Vacancies)
- Qualification: ITI/Diploma
- Experience: 1–2 years
- Responsibilities: Operate and maintain water systems, ensure purified water quality, and follow cGMP.
- Skills: Knowledge of water system operations and aseptic standards.
QMS Officer/Sr. Officer (3 Vacancies)
- Qualification: B.E./Diploma Mechanical
- Experience: 2–4 years
- Responsibilities: Manage QMS processes, ensure compliance, and support audits.
- Skills: Proficiency in QMS, documentation, and cGMP.
HVAC Operator (5 Vacancies)
- Qualification: ITI/Diploma
- Experience: 1–2 years
- Responsibilities: Maintain HVAC systems, ensure cleanroom conditions, and comply with cGMP.
- Skills: Expertise in HVAC maintenance and aseptic operations.
Microbiology Department
Environmental Monitoring Trainee/Officer/Sr. Officer (10 Vacancies)
- Qualification: B.Sc./M.Sc. Microbiology
- Experience: Fresher or 2–8 years
- Responsibilities: Conduct environmental monitoring, perform microbiological testing, and maintain aseptic standards.
- Skills: Knowledge of EM protocols, cGMP, and data integrity.
Production Department
Packing Officer (5 Vacancies)
- Qualification: B.Pharm/M.Pharm
- Experience: Fresher or 1 year
- Responsibilities: Oversee packing operations, ensure quality standards, and follow GDP.
- Skills: Familiarity with packing processes and cGMP.
QMS Officer/Sr. Officer (2 Vacancies)
- Qualification: B.Pharmacy
- Experience: 1–3 years
- Responsibilities: Manage QMS activities, ensure compliance, and support regulatory audits.
- Skills: Expertise in QMS and documentation.
Batch Manufacturing Operator (2 Vacancies)
- Qualification: D.Pharmacy
- Experience: Fresher or 1 year
- Responsibilities: Execute batch manufacturing, maintain cGMP, and ensure product quality.
- Skills: Knowledge of manufacturing processes and GDP.
Washing (Ampoule/Vial) Operator (2 Vacancies)
- Qualification: D.Pharmacy/ITI
- Experience: 2–3 years
- Responsibilities: Perform ampoule/vial washing, ensure sterility, and follow cGMP.
- Skills: Expertise in cleaning and aseptic techniques.
Eye Drops/Vial/Ampoule Filling Operator (4 Vacancies)
- Qualification: HSC + ITI (Fitter/Electrician/Machinist) or D.Pharmacy
- Experience: 2–3 years
- Responsibilities: Operate filling equipment, ensure sterile operations, and comply with cGMP.
- Skills: Proficiency in filling processes and aseptic behavior.
Autoclave/LYO Operator (4 Vacancies)
- Qualification: HSC + ITI (Fitter/Electrician/Machinist) or D.Pharmacy
- Experience: Fresher
- Responsibilities: Operate autoclave/LYO systems, maintain sterility, and follow cGMP.
- Skills: Knowledge of sterilization processes and GDP.
Garment Washing Operator (2 Vacancies)
- Qualification: 10th/12th Pass
- Experience: Fresher
- Responsibilities: Perform garment washing, ensure cleanroom standards, and follow SOPs.
- Skills: Understanding of cleanroom protocols and hygiene standards.
Liquid Injection/Packing Sr. Officer/Executive (3 Vacancies)
- Qualification: B.Pharm/M.Pharm
- Experience: 5–8 years
- Responsibilities: Oversee liquid injection and packing operations, ensure cGMP compliance.
- Skills: Expertise in injectable manufacturing and regulatory standards.
Quality Assurance (QA) Department
Lab QA Officer (1 Vacancy)
- Qualification: B.Pharm/M.Pharm
- Experience: 1–2 years
- Responsibilities: Review lab data, ensure cGMP compliance, and support audits.
- Skills: Proficiency in QA processes and documentation.
QMS Officer (1 Vacancy)
- Qualification: B.Sc./M.Sc./B.Pharm/M.Pharm
- Experience: 2–4 years
- Responsibilities: Manage QMS activities, handle deviations, and ensure compliance.
- Skills: Knowledge of QMS and regulatory standards.
IPQA/Validation Officer/Sr. Officer (3 Vacancies)
- Qualification: B.Pharm/M.Pharm
- Experience: 2–4 years
- Responsibilities: Conduct IPQA, perform validation, and support USFDA audits.
- Skills: Expertise in validation and cGMP compliance.
Quality Control (QC) Department
Stability – HPLC Officer/Sr. Officer (5 Vacancies)
- Qualification: B.Sc./M.Sc./B.Pharm
- Experience: 2–4 years
- Responsibilities: Perform HPLC analysis, conduct stability studies, and ensure cGMP compliance.
- Skills: Proficiency in HPLC and data integrity.
Validation Officer/Sr. Officer (5 Vacancies)
- Qualification: B.Sc./M.Sc./B.Pharm
- Experience: 2–4 years
- Responsibilities: Execute method validation, prepare validation reports, and follow cGMP.
- Skills: Expertise in validation processes and analytical techniques.
Warehouse Department
Raw Material & Packing Material Assistant (3 Vacancies)
- Qualification: 12th Pass
- Experience: Fresher
- Responsibilities: Assist in material handling, maintain inventory records, and follow GDP.
- Skills: Basic knowledge of warehouse operations and organization.
Raw Material & Packing Material Jr. Officer/Officer/Executive (5 Vacancies)
- Qualification: B.Com or Any Graduation
- Experience: 1–9 years
- Responsibilities: Manage material segregation, inventory, and ensure cGMP compliance.
- Skills: Expertise in warehouse management and documentation.
Why These Roles Matter
These roles ensure product quality, regulatory compliance, and operational efficiency in our US FDA-approved facility, directly impacting global healthcare standards.
Benefits of Joining Ciron Drugs
- Competitive salary and comprehensive benefits.
- Work in a US FDA and WHO-GMP certified facility.
- Exposure to global pharmaceutical standards.
- Collaborative and innovative work culture.
- Career growth in injectable manufacturing.
How to Apply
Attend the walk-in drive on June 28–29, 2025, from 10:00 AM to 2:00 PM at our Tarapur facility with required documents. Alternatively, email your CV to hrd@cironpharma.com or call 8010319276 / 9607989878 / 9168040418 / 8956866757.

Application Process
- Step 1: Attend the walk-in or email CV to hrd@cironpharma.com.
- Step 2: HR reviews applications for eligibility.
- Step 3: Interviews conducted during the walk-in event.
- Step 4: Final selection and offer process.
About Our Facility
Our Tarapur facility is US FDA and WHO-GMP certified, specializing in injectables, eye drops, and tablets. Learn more at Ciron Drugs.
Join Our Mission
Join Ciron Drugs to advance global healthcare. Attend our walk-in drive or apply today for roles in Engineering, Microbiology, Production, QA, QC, or Warehouse.