Ciron Drugs & Pharmaceuticals Pvt. Ltd., a USFDA-approved, Mumbai-based pharmaceutical leader established in 1966, is hosting a Walk-in Drive on June 21–22, 2025, at our Tarapur facility in Maharashtra.
We’re hiring for Microbiology, Production, Quality Assurance (QA), Quality Control (QC), Warehouse, and Engineering departments to support our mission of delivering high-quality, affordable generic formulations globally. Join our team at a state-of-the-art plant specializing in ampoules, vials, eye/ear/nasal drops, and lyophilized products.
About Ciron Drugs
Ciron Drugs is renowned for excellence in pharmaceutical manufacturing, with facilities in Tarapur and Palghar certified by USFDA, WHO-GMP, and ISO 9001:2008. Serving 50+ countries, we produce injectables, tablets, capsules, and lyophilized formulations, investing 40% of profits in advanced technology and training.
With 100+ employees and a 3.3/5 AmbitionBox rating, we offer a professional yet challenging work environment. Learn more at Ciron Drugs.
Walk-in Drive Details
We’re seeking freshers and experienced professionals for our Tarapur facility. Below are the event details:
| Event Details | Information |
|---|---|
| Date | June 21–22, 2025 (Saturday & Sunday) |
| Time | 10:00 AM to 2:00 PM IST |
| Venue | UNIT 1: N-118, N-119 & N-113, M.I.D.C., Tarapur, Boisar, Dist. Palghar – 401506, Maharashtra |
| Application Email | hrd@cironpharma.com |
| Contact Numbers | +91 8010319276, +91 9607989878, +91 9168040418 |
Job Opportunities
Below are the open positions, qualifications, experience, and responsibilities at our Tarapur Unit 1 facility. All roles are in a USFDA-approved environment.
1. Microbiology
- Section: Environmental Monitoring (EM)
- Designation: Trainee / Officer / Sr. Officer
- Qualification: B.Sc. / M.Sc. (Microbiology)
- Experience: Fresher, 2–8 years
- Vacancies: 10
- Responsibilities:
- Conduct environmental monitoring in cleanrooms (e.g., air sampling, surface swabs).
- Perform microbial testing and sterility checks for injectables.
- Ensure compliance with USFDA, cGMP, and SOPs.
- Skills: Knowledge of GLP, microbial limits testing, and cleanroom protocols.
2. Production
Section: Packing
- Designation: Officer
- Qualification: B.Pharm
- Experience: Fresher or 1 year
- Vacancies: 5
- Responsibilities:
- Oversee packing operations for vials, ampoules, and eye drops.
- Ensure line clearance and batch packing records accuracy.
- Skills: Familiarity with cGMP and packing line operations.
Section: QMS
- Designation: Officer / Sr. Officer
- Qualification: B.Pharm / M.Pharm
- Experience: 1–3 years
- Vacancies: 2
- Responsibilities:
- Implement QMS processes (e.g., CAPA, deviation handling).
- Support USFDA audit readiness and documentation.
- Skills: Expertise in QMS tools and regulatory compliance.
Section: Batch Manufacturing
- Designation: Operator
- Qualification: D.Pharm
- Experience: Fresher or 1 year
- Vacancies: 2
- Responsibilities:
- Operate reactors and mixers for batch manufacturing.
- Record BMR and maintain cGMP standards.
- Skills: Basic knowledge of batch processes and aseptic techniques.
Section: Washing (Ampoule/Vial)
- Designation: Operator
- Qualification: D.Pharm / ITI
- Experience: 2–3 years
- Vacancies: 2
- Responsibilities:
- Perform ampoule/vial washing and sterilization.
- Ensure cleanroom compliance and equipment upkeep.
- Skills: Experience with washing machines and cleanroom protocols.
Section: Eye Drops / Vial / Ampoule Filling
- Designation: Operator
- Qualification: HSC + ITI (Fitter/Electrician/Machinist) / D.Pharm
- Experience: 2–3 years
- Vacancies: 4
- Responsibilities:
- Operate filling machines for eye drops, vials, and ampoules.
- Maintain aseptic conditions and batch records.
- Skills: Proficiency in filling equipment and cGMP.
Section: Autoclave / LYO
- Designation: Operator
- Qualification: HSC + ITI (Fitter/Electrician/Machinist) / D.Pharm
- Experience: Fresher
- Vacancies: 4
- Responsibilities:
- Operate autoclaves and lyophilizers for sterilization and drying.
- Follow SOPs and maintain equipment logs.
- Skills: Basic understanding of sterilization and lyophilization.
Section: Garment Washing
- Designation: Operator
- Qualification: 10th/12th pass
- Experience: Fresher
- Vacancies: 2
- Responsibilities:
- Clean and sterilize cleanroom garments.
- Maintain hygiene standards and documentation.
- Skills: Attention to detail and cleanroom hygiene awareness.
Section: Liquid Injection / Packing
- Designation: Sr. Officer / Executive
- Qualification: B.Pharm / M.Pharm
- Experience: 5–8 years
- Vacancies: 3
- Responsibilities:
- Supervise liquid injection manufacturing and packing.
- Ensure USFDA compliance and batch release.
- Skills: Leadership and injectable manufacturing expertise.
3. Quality Assurance (QA)
Section: Lab QA
- Designation: Officer
- Qualification: B.Pharm / M.Pharm
- Experience: 1–2 years
- Vacancies: 1
- Responsibilities:
- Review lab data and test reports for compliance.
- Support audit preparation and SOP development.
- Skills: Knowledge of GLP and USFDA guidelines.
Section: QMS
- Designation: Officer
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm
- Experience: 2–4 years
- Vacancies: 1
- Responsibilities:
- Manage QMS activities (e.g., deviations, change controls).
- Ensure cGMP and audit readiness.
- Skills: Proficiency in QMS systems and documentation.
Section: IPQA / Validation
- Designation: Officer / Sr. Officer
- Qualification: B.Pharm / M.Pharm
- Experience: 2–4 years
- Vacancies: 3
- Responsibilities:
- Conduct IPQA checks and process validations.
- Document validation protocols for USFDA audits.
- Skills: Expertise in IPQA and validation processes.
4. Quality Control (QC)
Section: Stability – HPLC
- Designation: Officer / Sr. Officer
- Qualification: B.Sc. / M.Sc. / B.Pharm
- Experience: 2–4 years
- Vacancies: 5
- Responsibilities:
- Perform HPLC analysis for stability studies.
- Ensure cGMP-compliant documentation and instrument calibration.
- Skills: Proficiency in HPLC, stability testing, and GLP.
Section: Validation
- Designation: Officer / Sr. Officer
- Qualification: B.Sc. / M.Sc. / B.Pharm
- Experience: 2–4 years
- Vacancies: 5
- Responsibilities:
- Conduct analytical method validations and equipment qualifications.
- Prepare validation reports for regulatory submissions.
- Skills: Knowledge of validation protocols and USFDA standards.
5. Warehouse
Section: Raw Material & Packing Material (RM & PM)
- Designation: Assistant
- Qualification: 12th pass
- Experience: Fresher
- Vacancies: 3
- Responsibilities:
- Handle material receipt and storage.
- Maintain inventory records per SOPs.
- Skills: Basic inventory management and organization skills.
Section: Raw Material & Packing Material (RM & PM)
- Designation: Jr. Officer / Officer / Executive
- Qualification: B.Com / Any Graduation
- Experience: 1–9 years
- Vacancies: 5
- Responsibilities:
- Manage RM/PM dispensing and inventory control.
- Ensure cGMP-compliant documentation and audit readiness.
- Skills: Expertise in warehouse operations and SAP/ERP.
6. Engineering
Section: Plant Maintenance
- Designation: Officer / Sr. Officer
- Qualification: B.E. / B.Tech (Mechanical) / Diploma (Mechanical)
- Experience: 2–4 years
- Vacancies: 2
- Responsibilities:
- Perform preventive maintenance on production equipment.
- Troubleshoot mechanical issues in cleanrooms.
- Skills: Knowledge of mechanical systems and cGMP.
Section: Water System
- Designation: Operator
- Qualification: ITI / Diploma
- Experience: 1–2 years
- Vacancies: 5
- Responsibilities:
- Operate and maintain purified water systems.
- Conduct routine checks and log documentation.
- Skills: Familiarity with water systems and maintenance.
Section: QMS
- Designation: Officer / Sr. Officer
- Qualification: B.E. / Diploma (Mechanical)
- Experience: 2–4 years
- Vacancies: 3
- Responsibilities:
- Implement QMS for engineering processes.
- Support equipment qualification and audit compliance.
- Skills: Knowledge of QMS and regulatory standards.
Section: HVAC
- Designation: Operator
- Qualification: ITI / Diploma
- Experience: 1–2 years
- Vacancies: 5
- Responsibilities:
- Operate and maintain HVAC systems in cleanrooms.
- Ensure environmental controls meet USFDA standards.
- Skills: Expertise in HVAC operations and cleanroom maintenance.
Why Join Ciron Drugs?
Ciron offers a dynamic career in a USFDA-approved facility. Benefits include:
- Competitive Salary: Officers earn ₹3–8 LPA; Operators ₹1.5–3 LPA in Tarapur.
- Global Exposure: Work in a facility exporting to 50+ countries.
- Career Growth: Training in HPLC, QMS, and cleanroom operations.
- Challenges: Employees note poor career growth (2.9/5) and work-life balance (3.0/5).
- Work Environment: State-of-the-art plant with a 3.3/5 AmbitionBox rating.
Why These Roles Matter
These roles drive Ciron’s production of injectables and lyophilized products for global markets. Your work in microbiology, HPLC analysis, or HVAC maintenance ensures quality and compliance, supporting Ciron’s reputation in Tarapur’s 1,500+ pharma job ecosystem.
Growth Opportunities
Ciron invests in training for cGMP, USFDA audits, and equipment handling, but career growth is rated low (2.9/5). The Tarapur facility offers exposure to regulated markets, with challenges like limited promotions.
Work Environment
The Tarapur plant features cleanrooms, lyophilizers, and HPLC labs, fostering a safety-focused culture (3.8/5 job security). Expect shift work and a moderate work-life balance (3.0/5).
How to Attend
Join us on June 21–22, 2025, from 10:00 AM to 2:00 PM at Tarapur Unit 1. Bring:
- Updated CV.
- 1 passport-size photograph.
- Aadhar and PAN card copies.
- Last two months’ salary slips and CTC structure (if applicable).
If unable to attend, email your CV to hrd@cironpharma.com with the subject line “[Department] – [Designation]” (e.g., “Microbiology – Officer”). Contact +91 8010319276, +91 9607989878, or +91 9168040418 for queries.
Preparation Tips
- Microbiology: Highlight EM or sterility testing experience.
- Production: Detail ampoule filling or lyophilization expertise.
- QA/QC: Emphasize HPLC, validation, or IPQA skills.
- Warehouse/Engineering: Showcase SAP or HVAC maintenance knowledge.
- Prepare for questions like “How do you ensure cGMP in filling operations?” or “What is HPLC method validation?”
Important Disclaimer
Ciron Drugs maintains a transparent recruitment process. We do not charge fees or use free email services (e.g., Gmail, Yahoo) for job offers. Verify opportunities through hrd@cironpharma.com or +91 9168001140/41. Report suspicious activities via the same channels.
Stay Safe from Fraud
- Confirm offers through official Ciron channels.
- Avoid sharing personal or financial information with unverified sources.
- Contact HR for clarifications.
Why Tarapur?
Tarapur, Maharashtra, is a pharma manufacturing hub with 1,500+ jobs, hosting Ciron’s USFDA-approved facility. Its proximity to Mumbai (120 km) and robust infrastructure make it ideal for industrial careers.
Join Ciron’s Mission
Ciron Drugs is committed to providing quality, affordable pharmaceuticals globally. By joining our Tarapur team, you’ll contribute to USFDA-compliant manufacturing of life-saving formulations. Attend our walk-in drive on June 21–22, 2025, or apply online to start your journey!
Next Steps
Arrive early for registration. The selection process may include technical interviews (e.g., HPLC analysis, QMS processes) and document verification. Selected candidates will receive spot offers or follow-up communication.
Contact Us
For queries, email hrd@cironpharma.com, call +91 8010319276 / +91 9607989878 / +91 9168040418, or visit Ciron Contact.
Innovate with Ciron
Join Ciron Drugs to advance pharmaceutical manufacturing in a USFDA-approved facility. Attend our Walk-in Drive on June 21–22, 2025, in Tarapur and be part of our 100+ strong team!
