Centaur Hiring QA, R&D, AR&D

QA, R&D, AR&D Openings for BSc/MSc/B.Pharm in Ambernath | Centaur

Centaur hiring multiple QA, R&D, AR&D professionals (1–20 yrs) for its Ambernath API facility. Walk-in details, qualifications, and vacancies.

Centaur Pharmaceuticals is conducting a large-scale hiring drive for its API manufacturing facility in Ambernath. This recruitment covers multiple functions across Quality Assurance, Research and Development, Analytical Research and Development, and QMS. The company is looking for experienced professionals who can support GMP compliance, documentation accuracy, quality control systems, and research excellence. Candidates with experience in regulated API environments will find strong career alignment with Centaur’s operations, infrastructure, and global compliance standards.

Company Overview

Centaur Pharmaceuticals is a respected name in the pharmaceutical industry, known for its focus on API manufacturing, regulatory compliance, and consistent quality assurance practices. The company operates facilities accredited by leading global regulatory bodies such as USFDA, EDQM, and MHRA. Centaur maintains a structured quality system that supports precision, transparency, and adherence to international guidelines. The organization prioritizes continuous improvement, strong analytical competencies, and well-governed R&D systems.

Job Role & Responsibilities

Centaur is hiring across several levels and departments, including QA, R&D, AR&D, and QMS. Below is a structured breakdown to help applicants choose the right role.

QUALITY ASSURANCE

• Analytical QA Lead (Dy. Manager, 12–15 yrs)
  Oversees analytical documentation, compliance, review processes, and GMP governance.
• Analytical QA Reviewer (Executive/Sr. Executive, 7–10 yrs)
  Reviews analytical records, methods, and validations for compliance.
• Microbiology QA Reviewer (Executive/Sr. Executive, 7–10 yrs)
  Manages microbiology documentation and GMP-focused review activities.
• APQR Preparation (Executive/Sr. Executive, 8–10 yrs)
  Handles Annual Product Quality Review documentation and data compilation.
• Engg. QA & ITQA (Executive/Sr. Executive, 8–10 yrs)
  Oversees QA activities related to engineering and IT systems.
• Regulatory / Marketing Support (Executive/Sr. Executive, 8–10 yrs)
  Provides documentation, dossier support, and compliance data for global submissions.
• Control Sample & Stability Sample Management (Sr. Officer/Executive, 5–8 yrs)
  Handles sample storage, stability monitoring, and documentation.
• IPQA (Executive/Sr. Executive, 5–8 yrs)
  Performs in-process checks across API manufacturing lines.
• QMS (Executive/Sr. Executive, 5–8 yrs)
  Supports change control, deviation management, CAPA, and QMS documentation.
• Investigation Lead (Dy. Manager, 12–15 yrs)
  Leads investigations for deviations, OOS, OOT, and prepares compliance reports.

RESEARCH & DEVELOPMENT (R&D)

• Scientist / Group Leader (Chemist to Sr. Executive, 1–8 yrs)
  Executes API research activities, method development, and optimization.
• Asst. Manager to Sr. Manager (10–20 yrs)
  Leads R&D teams, manages project execution, and drives innovation.

ANALYTICAL RESEARCH & DEVELOPMENT (AR&D)

• Chromatography (Officer/Sr. Officer, 2–5 yrs)
  Hands-on HPLC experience, understanding of GDP and GLP.
• Wet Lab Analyst (Officer, 1–3 yrs)
  Executes KF, IR, UV, melting point testing, sample preparation, handling, and documentation.
• Chemist (1–2 yrs)
  Assists in routine analytical activities and documentation.

Eligibility / Qualifications

Accepted educational backgrounds include:

• B.Sc Chemistry, M.Sc Chemistry, B.Pharm, Ph.D Chemistry
• Additional relevant fields: Organic Chemistry, Analytical Chemistry, Industrial Chemistry, Pharmaceutical Chemistry

Preferred Candidate Profile:

• API pharmaceutical experience from regulated facilities (USFDA, EDQM, MHRA)
• Strong understanding of GMP, GLP, GDP, and documentation accuracy
• Readiness to work in all shifts

Location & Salary

Location: Centaur Pharmaceuticals Pvt Ltd, Chikhloli MIDC, Ambernath West, Maharashtra

Salary will depend on role, experience, and department. Industry-competitive packages will be offered.

Application Process

Candidates interested in the walk-in should bring:

• Updated CV
• One passport-size photograph

For other departments such as API Production, Safety, ETP, Maintenance, QC, and HR (4–6 yrs experience), resumes may be sent to:

• apihrd@centaurlab.com
• Contact: +91 251 6611900

Walk-In Drive Details

Date: Saturday, 13 December 2025
Time: 10 AM – 4 PM
Venue: Centaur Pharmaceuticals Pvt Ltd, Plot 75–76, Chikhloli MIDC, Ambernath West – 421501

FAQs

Can freshers apply?

These openings are intended for candidates with 1–20 years of API, QA, R&D, or AR&D experience.

Are shift duties mandatory?

Yes. Candidates must be willing to work in all shifts.

What regulatory experience is preferred?

Experience with USFDA, EDQM, and MHRA-compliant facilities is strongly preferred.

What skills improve shortlisting chances?

Strong documentation skills, GMP knowledge, analytical expertise, and experience in regulated API environments.

Is this walk-in mandatory?

Walk-in is recommended for faster shortlisting, but email submissions are accepted for other departments.

Summary Table

Category	Details
Company	Centaur Pharmaceuticals Pvt Ltd
Vacancies	Multiple roles across QA, R&D, AR&D, QMS
Required Education	B.Sc, M.Sc, B.Pharm, Ph.D Chemistry
Experience	1–20 years depending on position