Centaur Pharma Walk in QC, QA & Engineering

QC, QA, Engineering Jobs for M.Pharm in Pune

Centaur Pharma hiring QC, QA & Engineering professionals in Pune. M.Pharm, B.Pharm, MSc eligible. 4–16 years experience required.

Centaur Pharmaceuticals Pvt. Ltd. is conducting a large walk-in interview at its Pune manufacturing facility for experienced professionals across Quality Control, Quality Assurance, Production, and Engineering departments. This hiring drive is focused on strengthening Centaur’s USFDA and MHRA approved Oral Solid Dosage (OSD) manufacturing operations. Candidates with prior exposure to regulated pharmaceutical manufacturing environments are invited to attend and explore long-term career opportunities with a rapidly growing Indian pharmaceutical company.

This walk-in drive targets mid-level to senior professionals as well as freshers for select production trainee roles, offering exposure to regulatory audits, compliance-driven operations, and global quality systems.

Company Overview

Centaur Pharmaceuticals Pvt. Ltd. is one of India’s fast-growing pharmaceutical companies with a strong presence in regulated markets. The company operates a USFDA and MHRA approved OSD manufacturing facility in Pune, supplying high-quality formulations to domestic and international markets.

Centaur is known for its robust quality systems, regulatory compliance culture, and focus on continuous improvement. The organization follows global standards aligned with USFDA, MHRA, and EU regulatory requirements, making it an attractive employer for professionals seeking long-term growth in quality, compliance, and pharmaceutical manufacturing careers.

By joining Centaur, professionals become part of a healthcare-driven mission focused on delivering safe, effective, and affordable medicines worldwide.

Job Role & Responsibilities

Centaur Pharmaceuticals is hiring for multiple roles across Quality Control, Quality Assurance, Production, and Engineering departments. All roles are based at the Pune OSD manufacturing facility.

Quality Control Department

Officer / Senior Officer – Quality Control

Sections: RM, In-Process & Finished Products, Stability, AMV & AMT, GLP, QMS, Microbiology

Key Responsibilities

• Performing raw material, in-process, and finished product analysis
• Conducting stability studies and microbiological testing as applicable
• Handling analytical method validation and analytical method transfer
• Ensuring compliance with GLP and data integrity requirements
• Maintaining laboratory documentation and quality records
• Supporting regulatory audits and inspections (USFDA, MHRA, EU)

Experience: 4–8 Years

Qualification: M.Sc, B.Pharm, M.Pharm

Executive / Senior Executive – Quality Control

Sections: RM, In-Process & Finished Products, Stability, AMV & AMT, GLP, QMS, Microbiology

Key Responsibilities

• Reviewing analytical data and laboratory documentation
• Supporting investigation of OOS, OOT, and deviations
• Ensuring laboratory compliance with regulatory standards
• Training junior analysts and supporting continuous improvement initiatives

Experience: 8–12 Years

Qualification: M.Sc, B.Pharm, M.Pharm

Deputy Manager / Assistant Manager – Quality Control (Section Head)

Sections: RM, FG, Stability, GLP

Key Responsibilities

• Leading QC sections and managing analyst teams
• Overseeing laboratory compliance, data integrity, and audit readiness
• Reviewing and approving analytical reports and SOPs
• Acting as key point of contact during regulatory inspections

Experience: 12–16 Years

Qualification: M.Sc, B.Pharm, M.Pharm

Quality Assurance Department

Executive / Senior Executive – Quality Assurance

Sections: Validation, IPQA

Key Responsibilities

• Handling process validation, cleaning validation, and equipment qualification
• Performing in-process quality assurance activities
• Reviewing batch manufacturing records and validation protocols
• Supporting regulatory inspections and internal audits

Experience: 4–10 Years

Qualification: B.Pharm, M.Pharm, M.Sc

Assistant Manager / Deputy Manager – Quality Assurance

Sections: QMS, AQA

Key Responsibilities

• Managing quality management systems and annual product quality reviews
• Handling audits, deviations, CAPA, and change control systems
• Ensuring continuous compliance with regulatory requirements

Experience: 10–15 Years

Qualification: B.Pharm, M.Pharm, M.Sc

Production Department

Trainee Operator – Production (OSD)

Sections: Granulation, Compression, Coating, Packing

Key Responsibilities

• Assisting senior operators in OSD manufacturing activities
• Learning GMP-compliant production processes
• Supporting documentation and equipment operations

Experience: Fresher

Qualification: B.Sc, D.Pharm, ITI

Engineering Department

Officer / Executive – Engineering

Sections: OSD Process Equipment Maintenance, Engineering Training Coordination

Key Responsibilities

• Maintenance and troubleshooting of OSD manufacturing equipment
• Supporting preventive maintenance and calibration activities
• Coordinating technical training for engineering staff

Experience: 5–8 Years

Qualification: B.E, Diploma in Mechanical Engineering (DME)

Eligibility / Qualifications

Required Education

M.Sc, B.Pharm, M.Pharm, B.Sc, D.Pharm, ITI, B.E, Diploma in Mechanical Engineering

Mandatory Experience Criteria

• Experience in formulation regulated manufacturing companies is mandatory
• Exposure to USFDA, MHRA, or EU regulatory audits is required for experienced roles

Location & Salary

Job Location:
Centaur Pharmaceuticals Pvt. Ltd., Plot No. 4, International Biotech Park, Hinjewadi Phase II, Pune – 411057

Walk-in Date & Time:
01 February 2026 (Sunday) | 08:30 AM to 04:00 PM

Salary:
Salary will be offered as per industry standards and will be commensurate with experience, designation, and regulatory exposure.

Application Process

Interested candidates can directly walk in with a detailed resume and recent passport-size photograph.

Candidates who are unable to attend may send their CVs to:

• Email: hrdesk_pune@centaur.co.in
• Contact: +91-20-66739414

Centaur Pharmaceuticals does not charge any recruitment fees. Candidates are advised to beware of fraudulent calls or payment requests.

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Frequently Asked Questions (FAQs)

Is regulatory audit exposure mandatory?

Yes. Exposure to USFDA, MHRA, or EU audits is mandatory for experienced QC, QA, and Engineering roles.

Are freshers eligible for this walk-in?

Freshers are eligible only for the Production Trainee Operator role.

Where is the walk-in interview venue?

The interview will be held at Centaur Pharmaceuticals Pvt. Ltd., Hinjewadi Phase II, Pune.

Can I apply via email instead of attending the walk-in?

Yes. Candidates may email their resume to hrdesk_pune@centaur.co.in.

Career Growth at Centaur Pharmaceuticals

Working at a USFDA and MHRA approved facility provides professionals with high-value regulatory exposure. Careers in quality assurance, quality control, and engineering within regulated OSD plants offer strong long-term demand, high compensation potential, and global mobility.

Centaur Pharmaceuticals supports continuous learning, leadership development, and career progression, making it an ideal organization for ambitious pharma professionals.

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Summary Table

Category	Details
Company	Centaur Pharmaceuticals Pvt. Ltd.
Vacancies	QC Officer/Sr. Officer, QC Executive/Sr. Executive, QC Asst. Manager/Deputy Manager, QA Executive/Sr. Executive, QA Asst. Manager/Deputy Manager, Production Trainee Operator, Engineering Officer/Executive
Required Education	M.Sc, B.Pharm, M.Pharm, B.Sc, D.Pharm, ITI, B.E, DME
Experience	Fresher to 16 Years (Role dependent)