India's DMPLOI - Jobs & Networking AppConcord Biotech, one of India’s leading biotechnology and pharmaceutical companies, has announced a Walk-In Interview Drive for experienced professionals in Regulatory Affairs, Analytical Development Laboratory (ADL-OSD), and Quality Assurance (QA). This recruitment drive offers excellent career opportunities for candidates looking to work in a dynamic and innovation-driven pharmaceutical environment.
The company is seeking talented professionals with relevant experience in regulatory submissions, analytical method development, stability studies, and quality assurance activities. Candidates who meet the eligibility criteria are encouraged to attend the interview with updated documents.
Walk-In Interview Details
Interview Date: 13 June 2026
Time: 10:00 AM to 2:00 PM
Location: Concord Biotech, Valthera, Dholka, Ahmedabad, Gujarat
Departments Hiring
1. Regulatory Affairs
Positions:
Executive
Sr. Executive
Assistant Manager
Deputy Manager
Manager
Sr. Manager
Qualification:
M.Sc.
B.Pharm
M.Pharm
Experience:
6 to 12 Years
Key Responsibilities:
Preparation and review of regulatory dossiers.
Product registration and lifecycle management.
Regulatory gap analysis and query response management.
Coordination with global regulatory agencies.
CDSCO, FDA, COPP, Loan License, and SUGAM portal-related activities.
2. Analytical Development Laboratory (ADL-OSD)
Chemist / Officer / Sr. Officer
Qualification: M.Sc. / M.Pharm
Experience: 2 to 4 Years
Executive / Sr. Executive
Qualification: M.Sc. / M.Pharm
Experience: 5 to 10 Years
Key Responsibilities:
Method development and validation.
Routine analysis of raw materials and finished products.
Stability studies and method transfer activities.
Operation of HPLC, GC, UV, Dissolution, Particle Size Analyzer, and ICP-OES.
Compliance with GDP and GLP requirements.
3. Quality Assurance (QA)
Position:
Officer / Sr. Officer
Qualification:
B.Pharm / M.Pharm
Experience:
5 to 8 Years
Key Responsibilities:
Stability sample management and documentation.
Preparation of stability protocols and schedules.
Handling retained samples and control samples.
Monitoring stability chambers and maintaining records.
Ensuring compliance with GMP requirements.
Documents Required
Candidates attending the walk-in interview should carry:
Updated CV/Resume
Current Salary Proof
Passport Size Photograph
Educational and Experience Certificates
Candidates unable to attend the interview can send their profiles via email by mentioning the applied position in the subject line.
Why Join Concord Biotech?
Concord Biotech is recognized for its strong presence in biotechnology and pharmaceutical manufacturing. The company provides a collaborative work environment, opportunities for professional growth, exposure to global regulatory standards, and involvement in cutting-edge pharmaceutical development projects.
This hiring drive is an excellent opportunity for experienced professionals seeking long-term career advancement in the pharmaceutical industry.
Technical FAQs
1. What is the difference between method validation and method verification in pharmaceutical analysis?
Method Validation establishes documented evidence that an analytical method consistently produces reliable results for its intended use. Method Verification confirms that a validated compendial method performs suitably under a laboratory’s specific conditions.
2. Why is dissolution testing important in OSD product development?
Dissolution testing evaluates the rate and extent of drug release from a dosage form. It is critical for formulation optimization, stability assessment, bioequivalence support, and regulatory compliance.
3. What is a regulatory dossier in pharmaceutical submissions?
A regulatory dossier is a structured collection of documents containing quality, safety, efficacy, manufacturing, and labeling information submitted to health authorities for product approval and registration.
4. What are GDP and GLP requirements in analytical laboratories?
GDP (Good Documentation Practices) ensures data integrity and traceability, while GLP (Good Laboratory Practices) ensures laboratory operations, testing procedures, equipment usage, and documentation meet quality standards.
5. What is the purpose of stability studies in pharmaceutical products?
Stability studies determine how environmental factors such as temperature, humidity, and light affect a drug product over time. These studies establish shelf life, storage conditions, and product quality throughout its lifecycle.
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