Centaur Walk-in QC, QA, Production

BPharm 50+ Vacancies Centaur Pharma Goa Pune Walk-in

B.Pharm, M.Pharm, M.Sc candidates apply for 50+ vacancies at Centaur Pharma Goa & Pune. QC, QA, Production jobs.

Centaur Pharmaceuticals Pvt. Ltd. is conducting a large-scale walk-in interview drive for multiple departments including Quality Control, Quality Assurance, Production, Warehouse, Engineering, and IT. This is a high-potential opportunity for candidates looking for pharma jobs in Goa and Pune, especially in OSD manufacturing, GMP compliance, and regulatory pharmaceutical careers.

If you are aiming for high-paying pharma roles such as QC analyst jobs, QA validation roles, GMP production jobs, or HPLC-based analytical careers, this hiring drive offers excellent exposure to USFDA/EU-GMP environments and long-term career growth.

Company Overview

Centaur Pharmaceuticals is a well-established pharmaceutical company known for its strong commitment to quality, compliance, and innovation. With advanced manufacturing facilities in Goa and Pune, the company specializes in Oral Solid Dosage (OSD) formulations and operates under stringent regulatory frameworks including USFDA and EU-GMP.

The organization focuses on delivering high-quality medicines globally, ensuring patient safety and regulatory compliance. Centaur provides professionals with hands-on experience in regulated environments, making it a preferred employer for pharma professionals seeking growth in manufacturing, quality assurance, and analytical domains.

Job Role & Responsibilities

Production & Packing (OSD Manufacturing)

• Handle granulation, compression, coating, inspection, and packing operations
• Manage blister and bottle packing lines
• Ensure adherence to GMP and production schedules
• Maintain documentation for batch manufacturing and dispensing

Quality Control (QC)

• Perform analysis using HPLC, GC, and other analytical instruments
• Conduct stability testing, AMV, AMT, and raw material analysis
• Handle QC review and documentation processes
• Ensure compliance with GLP and regulatory standards

Quality Assurance (QA)

• Manage IPQA, cleaning validation, and process validation
• Handle QMS activities including deviations, CAPA, and investigations
• Conduct audits and ensure compliance with regulatory guidelines
• Support technology transfer and documentation processes

Warehouse & Documentation

• Manage RM/PM handling, documentation, and QMS processes
• Ensure inventory control and compliance with GDP practices

Engineering & IT

• Maintain plant utilities and manufacturing equipment
• Support IT infrastructure and pharma documentation systems

These roles are critical in ensuring the production of safe, effective, and compliant pharmaceutical products.

Eligibility / Qualifications

Required Education:

• B.Pharm
• M.Pharm
• M.Sc
• B.Sc
• Diploma
• B.E / B.Tech
• BCA / MCA

Relevant Courses:

Pharmaceutics, Pharmaceutical Analysis, Microbiology, Industrial Pharmacy, Mechanical Engineering, Electrical Engineering, Computer Applications

Experience Required:

• Production & Packing: 3–7 Years
• QC / QA / Warehouse: 3–16 Years
• Engineering / IT: 3–8 Years

Skills Required:

• GMP, GDP, and QMS compliance
• HPLC, GC, analytical testing
• OSD manufacturing processes
• Documentation, validation, and investigation handling
• Experience in USFDA/EU-GMP plants preferred

Location & Salary

• Job Locations: Goa (Tuem) & Pune (Hinjewadi)

Salary:

• Competitive salary based on experience
• Additional benefits as per company policy

Application Process

Walk-in Interview Details:

• Date: 03 May 2026 (Sunday)
• Time: 09:00 AM – 04:00 PM

Interview Venue:

Centaur Pharmaceuticals Pvt. Ltd.
Plot No. 60, Tuem Industrial Estate
Pernem, Goa – 403512

Email Applications:

• Goa: tuem_hr@centaurgoa.com
• Pune: hrpune@centaur.co.in

Documents Required:

• Updated Resume
• Passport Size Photograph
• Last 3 Months Salary Slips
• Appointment / Increment Letters
• Educational Certificates (Original & Copy)
• ID Proof

Important Notes:

• Registration is mandatory
• No TA/DA will be provided
• Candidates must be flexible for shift work

Why Join Centaur Pharmaceuticals?

• Work in USFDA and EU-GMP compliant facilities
• Exposure to OSD manufacturing and global pharma standards
• Strong career growth in QC, QA, and production domains
• Opportunities in analytical, validation, and regulatory roles
• Stable career path in high-demand pharmaceutical sectors

These roles contribute directly to global healthcare by ensuring the quality and safety of medicines supplied worldwide.

FAQs

Who can apply for Centaur Pharma jobs?

Candidates with B.Pharm, M.Pharm, M.Sc, B.Sc, Diploma, B.Tech, BCA, or MCA qualifications.

What experience is required?

3–16 years depending on the role.

What skills are important?

GMP compliance, HPLC/GC analysis, QMS documentation, and OSD manufacturing expertise.

Is regulatory plant experience required?

Preferred, especially experience in USFDA or EU-GMP environments.

Are multiple locations available?

Yes, roles are available in Goa and Pune.

Final Thoughts

This Centaur Pharmaceuticals walk-in drive is ideal for professionals aiming to advance their careers in pharmaceutical manufacturing, quality control, and regulatory compliance.

With rising demand for skilled professionals in OSD manufacturing, QC analysis, and QA validation, these roles offer strong salary potential, career stability, and global exposure.

If you are targeting high-CPC pharma keywords such as QC analyst jobs, QA validation roles, GMP pharma jobs, or HPLC jobs in India, this opportunity is highly valuable.

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Company	Centaur Pharmaceuticals Pvt. Ltd.
Vacancies	QC Officer, QA Executive, Production Executive, Engineer, IT Officer
Required Education	B.Pharm, M.Pharm, M.Sc, B.Sc, Diploma, B.Tech, BCA, MCA
Experience	3–16 Years