Centaur Hiring QC, Production & Packaging

M.Sc/B.Sc — QC, Production & Packaging Roles at Centaur Pune

M.Sc/B.Sc/D.Pharm candidates: Multiple openings at Centaur Pharmaceuticals, Pune for QC, Production, Packaging. Apply with experience details.

Centaur Pharmaceuticals Pvt. Ltd., Pune is recruiting across Quality Control, Production, and Packaging Development to support its fast growth in specialty and regulated markets. These roles suit experienced analytical and operations professionals as well as entry-level production trainees. If you work with oral solid dosage forms, stability studies, or packaging development — this is a targeted opportunity to join a WHO/USFDA-facing manufacturer.

Company Overview

Centaur Pharmaceuticals is a leading specialty drug manufacturer in India with a reputation for quality and regulatory compliance. The company supplies formulations that meet international standards and has experience engaging with major regulators like USFDA and MHRA. Centaur’s Pune site focuses on oral solid dosage manufacturing and supports a range of regulated markets. Working here provides exposure to validated processes, stability programs, and technical packaging development — valuable for long-term careers in QC, production, and R&D.

Open Positions & Job Role Details

Centaur is hiring for multiple positions at its Pune facility. Below are the specific roles, sections, qualifications, and experience required.

1. Quality Control — Sr. Executive / Assistant Manager (Stability / RM / PM / GLP / AMV / AMT)

Qualification: M.Sc. (Chemistry)
Experience: 12–14 years

Responsibilities:

• Lead stability program management, oversee long-term and accelerated study execution and data review.
• Supervise raw material (RM), product method (PM), finished product (FP) testing and GLP-compliant lab practices.
• Ensure ALCOA+ data integrity, manage method validation (AMV) and analytical method transfer (AMT) activities.
• Drive continuous improvement in QC processes, mentor junior analysts, and interface with QA for release decisions.
• Coordinate with regulatory teams for dossier quality sections and respond to audit queries.

Why this role matters: Senior QC leadership ensures data credibility, method robustness, and regulatory readiness — critical when supplying regulated markets.

2. Quality Control — Officer / Sr. Officer (Stability / RM / PM / FP / GLP / AMV / AMT)

Qualification: M.Sc. (Chemistry)
Experience: 4–8 years

Responsibilities:

• Perform routine and stability testing for oral solid dosage forms.
• Execute method validation/verification and support analytical method transfer.
• Maintain instrument calibration and troubleshooting for HPLC, UV, and other analytical equipment.
• Ensure adherence to cGMP and GLP standards, accurate record-keeping, and timely reporting of results.

Why this role matters: QC officers maintain day-to-day analytical integrity and play a direct role in batch release and stability claims.

3. Production — Trainee Operator (Granulation / Compression / Packing)

Qualification: ITI / B.Sc / D.Pharm
Experience: Fresher

Responsibilities:

• Assist operators in granulation, compression, and packing operations for oral solids.
• Follow SOPs for equipment setup, in-process checks, and line clearance.
• Learn GMP behavior, cleanroom practices, and basic documentation for batch records.
• Support preventive maintenance and housekeeping for production lines.

Why this role matters: Entry-level operators are the backbone of manufacturing; the role is a practical training ground for skilled production careers.

4. Packaging Development Executive (Packaging Development)

Qualification: B.Sc / B.Pharm / Diploma in Packaging Technology
Experience: 6–10 years

Responsibilities:

• Lead packaging development projects for new and existing oral solid products.
• Design and test primary and secondary packaging, ensure compatibility and stability under regulatory conditions.
• Coordinate artwork, material selection, supplier qualification, and packaging validations.
• Work with QA and Regulatory to ensure packaging meets global market requirements.

Why this role matters: Packaging decisions affect product stability, patient safety, and regulatory acceptability — making this a strategic technical function.

Eligibility / Qualifications (All Positions)

• Preferred disciplines: M.Sc (Chemistry), B.Sc, B.Pharm, D.Pharm, ITI, Diploma in Packaging Technology.
• Core skills: cGMP knowledge, documentation discipline, method validation basics (for QC), hands-on production experience (for production roles), packaging testing and material science understanding (for packaging role).

Relevant courses (comma-separated): M.Sc Chemistry, B.Sc Chemistry, B.Pharm, M.Pharm Pharmaceutical Analysis, D.Pharm, ITI Mechanical/Pharma, Diploma in Packaging Technology, PG Diploma in Quality Assurance, B.Sc Biotechnology

Location & Salary

• Location: Pune site (exact campus/location to be confirmed during recruitment communication).
• Salary: Not specified in HR brief — competitive and aligned with experience and role level. Centaur typically offers market-linked compensation for specialized QC and packaging roles.

Application Process

Share your updated resume by email to:

• Email: nkadam@centaur.co.in

Email subject suggestion: Application — [Position Title] — [Your Name]

In your email, explicitly mention the section you are applying for (e.g., Stability / Packaging), total years of experience, and key technical skills (e.g., stability program management, HPLC method validation, granulation operations, packaging validations).

EEAT & Impact Statement

Centaur’s focus on regulated markets demands technical accuracy and transparent data practices. Each role contributes directly to product quality, regulatory submissions, and patient safety. Senior QC roles strengthen the company’s authoritativeness in analytical claims; packaging development preserves product integrity during distribution; production trainees ensure reliable manufacturing throughput. Together, these functions align with Google’s EEAT principles by building demonstrable expertise, operational authority, and trustworthy product stewardship.

High-CPC Keywords Included Naturally

pharmaceutical jobs, QC analyst jobs, HPLC method validation, stability scientist jobs, packaging development engineer, GMP manufacturing jobs, oral solid dosage manufacturing, pharma production trainee, packaging validation, regulatory submission support.

How to Stand Out — Application Tips (Quick & Direct)

• Tailor your resume to the section: list stability studies, method validations, or packaging projects with measurable outcomes.
• For QC roles, mention specific instruments (HPLC, GC, KF) and validation reports you contributed to.
• For packaging roles, include examples of material compatibility tests, shelf-life studies, and supplier qualifications.
• For production trainees, highlight practical lab coursework, internships, or vocational training.
• Keep CV concise (2 pages max for experienced; 1 page for freshers), use bullet points, and include contactable references.

FAQs

Q: Are remote or hybrid roles available?
A: No. These are on-site manufacturing and laboratory roles requiring presence at the Pune facility.

Q: What is the selection process?
A: Shortlisting based on CV, followed by telephonic interview and on-site technical interview/HR discussion.

Q: Are freshers eligible for any position?
A: Yes — the Production Trainee Operator role accepts freshers with ITI/B.Sc/D.Pharm qualifications.

Q: What documents should I attach?
A: Updated CV, experience certificates, and educational documents on request.

Q: Is relocation support provided?
A: Not specified in the HR brief. Mention relocation willingness in your cover mail if applicable.

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Category	Details
Company	Centaur Pharmaceuticals Pvt. Ltd., Pune
Vacancies	QC Sr. Executive/Asst.Manager (Stability), QC Officer/Sr. Officer, Production Trainee Operator (Granulation/Compression/Packing), Packaging Development Executive
Required Education	M.Sc Chemistry, B.Sc Chemistry, B.Pharm, M.Pharm, D.Pharm, ITI, Diploma in Packaging Technology
Experience	12–14 yrs (Sr QC), 4–8 yrs (QC Officer), Fresher (Production Trainee), 6–10 yrs (Packaging Dev)