Ciron Drugs & Pharmaceuticals walk-in alert! A USFDA-approved pharmaceutical company is hiring Officer / Sr. Officer / Executive positions in the Quality Control (QC) department at its Unit-1 facility in Tarapur, Boisar, Maharashtra.
This is an excellent opportunity for candidates with 2–8 years of experience seeking QC jobs, pharma jobs, HPLC jobs, analytical chemistry roles, and stability section vacancies in Maharashtra.
Total Vacancies: 10
Contents
About the Company
Ciron Drugs & Pharmaceuticals Pvt. Ltd. is a USFDA-approved manufacturer of high-quality pharmaceutical formulations and APIs. With state-of-the-art facilities in Tarapur, Boisar (Maharashtra), the company specializes in developing and manufacturing a wide range of sterile and non-sterile products for both domestic and international markets.
Known for its strong focus on quality, regulatory compliance, and timely delivery, Ciron has earned approvals from major global authorities including the USFDA. The company is committed to maintaining the highest standards of GMP and GLP while continuously investing in advanced analytical instruments and infrastructure to meet evolving customer and regulatory requirements.
Job Details
- Company Name: Ciron Drugs & Pharmaceuticals Pvt. Ltd.
- Department: Quality Control (QC)
- Position: Officer / Sr. Officer / Executive
- Experience: 2 to 8 years
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm
- Total Vacancy: 10
- Location: Tarapur, Boisar, Dist. Palghar, Maharashtra
- Work Type: On-site
Job Description
Ciron Drugs is looking for experienced professionals to strengthen its Quality Control team. The roles cover multiple sections including Analytical Method Validation (AMV), Raw Material, Finished Product, Stability, and GLP sections. Candidates will be responsible for handling sophisticated instruments such as HPLC and GC while ensuring compliance with regulatory standards.
Officer / Sr. Officer / Executive – Quality Control
- Department: Quality Control
- Section: AMV, Raw Material, Finished Product, Stability Section, GLP Section (Handling Instruments like HPLC / GC)
- Designation: Officer / Sr. Officer / Executive
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm
- Experience: 2 to 8 years
Skills/Qualifications
- Hands-on experience in Analytical Method Validation (AMV)
- Strong knowledge of Raw Material (RM) and Finished Product (FP) analysis
- Experience in stability studies and GLP documentation
- Proficiency in operating and troubleshooting HPLC and GC instruments
- Good understanding of GMP, GLP, ICH guidelines, and regulatory requirements
- Excellent documentation and data integrity skills
- Ability to work independently and manage multiple sections effectively
Key Responsibilities
- Perform analysis of Raw Materials, Finished Products, and Stability samples
- Conduct Analytical Method Validation and verification activities
- Operate and maintain HPLC and GC instruments
- Ensure compliance with GLP and cGMP requirements
- Maintain accurate records, calibration logs, and documentation
- Support investigations, OOS/OOT, and CAPA activities
- Contribute to audit readiness and regulatory compliance
Benefits/Perks
- Work with a USFDA-approved pharmaceutical manufacturing company
- Career growth in a well-established QC department with multiple sections
- Exposure to advanced analytical instruments and global quality standards
- Stable employment with opportunities for learning and advancement
- Professional work environment focused on quality and compliance
For more QC jobs and pharma jobs in Maharashtra, explore current openings on Pharma Recruiter.
How to Apply
Candidates can attend the walk-in interview directly at the venue or share their CV via email/phone.
- Email: hrd@cironpharma.com / hr.plant1@cironpharma.com
- Mobile: 8010319276 / 9356969478 / 9607989878
- Landline: 9168001140 / 41 (Ext. 254)
Please mention “QC Officer / Executive” in the subject line while sending your CV.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Ciron Drugs LinkedIn page.
Apply now and join a USFDA-approved leader in pharmaceutical manufacturing!
Walk-in Interview Details
- Venue: UNIT 1: N-118, N-119 & N-113, M.I.D.C., Tarapur, Boisar, Dist. Palghar – 401506, Maharashtra
Why You Should Join
Ciron Drugs & Pharmaceuticals offers a stable and growth-oriented platform for QC professionals. With USFDA approval and modern analytical infrastructure, the company provides excellent opportunities to work on diverse product portfolios while building expertise in high-standard quality control practices.
Joining Ciron means contributing to quality medicines that reach patients worldwide while advancing your career in a regulated, quality-focused environment.
FAQs
What is the experience required for Ciron QC positions?
2 to 8 years in Quality Control, preferably with experience in AMV, HPLC, GC, stability, or raw material analysis.
What qualifications are accepted?
B.Sc., M.Sc., B.Pharm, or M.Pharm.
How many vacancies are available?
Total 10 vacancies in the Quality Control department.
Can I apply by email if I cannot attend the walk-in?
Yes, you can send your CV to hrd@cironpharma.com or hr.plant1@cironpharma.com.
