Cadila Hiring QC Officers/Executives

Pharma Stuff; Gujarat; On-site; INR 300,000 - 540,000; Full time

Job summary

Cadila Pharmaceuticals is hiring QC Officers/Executives for its Dholka formulation manufacturing facility in Gujarat. Candidates with 1–5 years of QC experience (BSc/MSc/BPharm) are encouraged to apply for a virtual interview on 24 December 2025.

The role focuses on analytical accuracy, regulatory compliance, and data integrity across QC operations, with assignments to HPLC, microbiology, chemical analysis, or stability sections as required.

Qualifications

• B.Sc, M.Sc, or B.Pharm required with 1–5 years of formulation QC experience.
• Hands-on exposure to HPLC, microbiology, chemical analysis, or stability testing as per assigned role.
• Working knowledge of GMP, GLP and data integrity requirements in cGMP environments.

Responsibilities

• Perform routine and non-routine analysis of finished products and stability samples.
• Conduct HPLC analysis, microbiology testing, and other QC analyses per SOPs.
• Maintain analytical records, logbooks, and reports with strict data integrity.
• Support investigations related to OOS/OOT and deviations.
• Participate in audits and cross-functional quality reviews.

Skills

GMP/GLP

Documentation

Data integrity

Regulated environment

Analytical instruments

Education

B.Sc

M.Sc

B.Pharm

Tools

HPLC

Microbiology Lab

Stability testing

Chemical analysis

Job description

BSc/MSc/BPharm QC Jobs (1–5 yrs) | Cadila Dholka

Cadila Pharmaceuticals hiring QC Officers/Executives in Dholka. BSc/MSc/BPharm with 1–5 years experience. Virtual interview on 24 Dec 2025.

Cadila Pharmaceuticals Limited has announced a virtual hiring drive for experienced Quality Control professionals at its Dholka formulation manufacturing facility. This opportunity is ideal for candidates with hands-on exposure to pharmaceutical quality control operations who are looking to build long-term careers with one of India’s most respected and research-driven pharmaceutical companies. The hiring focuses on core QC functions including HPLC analysis, microbiology testing, chemical analysis, and stability studies within a regulated formulation environment.

This opening is especially relevant for professionals actively searching for quality control jobs in pharma, QC analyst roles in formulation plants, microbiology QC positions, and HPLC analyst jobs in Gujarat. The virtual interview format allows qualified candidates to participate remotely while accessing a stable and growth-oriented organization recognized as a Great Place to Work.

Company Overview

Cadila Pharmaceuticals Limited is a globally recognized Indian pharmaceutical company with a strong presence across formulations, APIs, biotechnology, and specialty therapies. With decades of experience in delivering affordable and high-quality medicines, Cadila operates multiple WHO‑GMP and regulatory-compliant manufacturing facilities catering to domestic and international markets.

The organization has been consistently certified as a Great Place to Work, reflecting its focus on employee well‑being, ethical practices, and professional development. Cadila’s Dholka plant is a key formulation manufacturing site supporting large-scale production while maintaining strict compliance with quality, safety, and regulatory standards.

Working at Cadila means contributing directly to patient safety, product quality, and healthcare accessibility while gaining exposure to robust quality systems and modern analytical infrastructure.

Job Role & Responsibilities

The Quality Control Officer/Executive role is responsible for ensuring analytical accuracy, regulatory compliance, and data integrity across formulation quality operations. Selected candidates will be aligned to specific QC sections based on expertise and business requirements.

Key Responsibilities

• Perform routine and non-routine analysis of finished products, in-process samples, and stability samples.
• Execute HPLC analysis, wet chemical testing, and instrumental analysis as per approved specifications.
• Conduct microbiological testing including environmental monitoring, microbial limit testing, and related QC activities (for microbiology section).
• Handle stability studies, sample pulls, documentation, and trend analysis.
• Prepare, review, and maintain analytical records, logbooks, and test reports in compliance with cGMP and data integrity norms.
• Support investigations related to OOS, OOT, deviations, and corrective actions.
• Ensure strict adherence to SOPs, quality systems, and regulatory guidelines.
• Coordinate with cross-functional teams during audits, inspections, and internal quality reviews.

This role demands precision, documentation discipline, and a strong understanding of pharmaceutical formulation quality systems.

Eligibility / Qualifications

Educational Background

Candidates must possess one of the following qualifications:

B.Sc, M.Sc, B.Pharm

Experience Requirements

• 1 to 5 years of relevant experience in pharmaceutical Quality Control.
• Mandatory experience in pharmaceutical formulation QC environments.
• Exposure to HPLC, microbiology, chemical analysis, or stability sections is required depending on the assigned role.

Key Skills

• Strong understanding of GMP, GLP, and pharmaceutical quality systems.
• Hands‑on experience with analytical instruments and laboratory procedures.
• Sound knowledge of documentation practices and data integrity requirements.
• Ability to work in regulated manufacturing environments with minimal supervision.

Location & Salary

• Job Location: Dholka Plant, Gujarat
• Employment Type: Full‑time
• Salary: Competitive and aligned with industry standards. Compensation is based on experience, skill set, and internal benchmarks.

Frequently Asked Questions (FAQs)

Who can apply for this QC role?
Candidates with B.Sc, M.Sc, or B.Pharm qualifications and 1–5 years of formulation QC experience are eligible.

Is API experience acceptable?
No. Only candidates with pharmaceutical formulation QC experience will be considered.

Is this a virtual interview?
Yes. The interview will be conducted online on 24 December 2025.

Which QC sections are hiring?
HPLC, Microbiology, Chemical Analysis, and Stability.

Is Cadila a stable organization for long-term careers?
Yes. Cadila Pharmaceuticals is a well-established company with strong regulatory compliance and employee‑centric practices.