Cadila Pharmaceuticals Ltd., one of India’s largest privately-held pharmaceutical companies, headquartered in Ahmedabad, Gujarat, is hosting a Walk-In Interview for talented professionals to join our innovative teams. With a legacy of over seven decades and a global presence in more than 100 countries, we are committed to developing affordable, high-quality medicines. Join us to contribute to groundbreaking work in Analytical Development Lab (ADL), Packaging Development, Project Management (PMO), Regulatory Affairs, Oral Solid Dosage (OSD) F&D, and Injectable F&D at our Ahmedabad facility
Interview Details
- Date: Sunday, April 27, 2025
- Time: 9:30 AM to 4:30 PM
- Venue: IRM House, Chimanlal Girdharlal Rd, Mithakhali, Navrangpura, Ahmedabad, Gujarat 380009
- Documents Required:
- Updated resume
- Educational certificates
- Experience certificates
- Recent payslips (if applicable)
- Aadhar and PAN card copies
- Contact:
- Email: shardulsinh.k@cadilapharma.com
- Phone: +91 958-615-7671
- Note: Candidates unable to attend can email their CV to the above address with the subject line indicating the department and position (e.g., “Application for ADL Research Associate”).
Why Join Cadila Pharmaceuticals?
Cadila Pharmaceuticals is a USFDA-approved, innovation-driven company with a 3.4/5 employee rating on AmbitionBox, reflecting a commitment to research and quality. By joining us, you will:
- Work in a state-of-the-art R&D facility in Dholka, Ahmedabad, staffed by over 300 scientists
- Contribute to first-in-the-world innovations like Risorine, Polycap, and Rabeloc IV
- Collaborate with a global team across therapeutic areas like oncology, cardiology, and infectious diseases
- Enjoy a supportive work environment with opportunities for career growth, though some reviews note scope’)){ for improvement in work culture
Available Positions
1. Analytical Development Lab (ADL) – Method Development / Method Validation / HPLC
- Positions: Research Associate / Deputy Manager / Principal Scientist
- Qualification: M.Sc. / M.Pharm / Ph.D.
- Experience: 3–7 years
Key Responsibilities:
- Develop and validate analytical methods using HPLC, GC, and other techniques
- Perform stability studies and method transfer for APIs and formulations
- Ensure compliance with cGMP and regulatory guidelines (USFDA, ICH)
- Document protocols, reports, and SOPs
Required Skills:
- Expertise in HPLC method development and validation
- Familiarity with analytical instruments (UV, IR, LC-MS)
- Strong knowledge of regulatory requirements
- Open Positions: Multiple
2. Packaging Development
- Positions: Executive / Senior Executive / Assistant Manager / Deputy Manager
- Qualification: Postgraduate Diploma in Packaging (IIP or SIES)
- Experience: 1–5 years in oral solid and liquid dosage form packaging development
Key Responsibilities:
- Design and develop packaging solutions for oral solids (tablets, capsules) and liquids
- Conduct stability and compatibility studies for packaging materials
- Optimize packaging processes to ensure product safety and regulatory compliance
- Collaborate with vendors and cross-functional teams
Required Skills:
- Knowledge of packaging materials (blisters, bottles, films)
- Understanding of cGMP and stability testing
- Experience with regulatory requirements for packaging
- Open Positions: Multiple
3. Project Management (PMO)
- Positions: Executive / Senior Executive / Assistant Manager / Deputy Manager
- Qualification: M.Pharm
- Experience: 3–7 years
Key Responsibilities:
- Plan and manage R&D and manufacturing projects from initiation to completion
- Coordinate cross-functional teams (R&D, QA, production) to meet timelines
- Track project milestones, budgets, and deliverables
- Prepare project documentation and reports for regulatory submissions
Required Skills:
- Strong project management skills (PMP certification is a plus)
- Knowledge of pharmaceutical R&D and manufacturing processes
- Excellent communication and organizational skills
- Open Positions: Multiple
4. Regulatory Affairs
- Positions: Executive / Senior Executive / Assistant Manager / Deputy Manager
- Qualification: M.Sc. / M.Pharm
- Experience: 3–7 years in DMF/CEP filing for global markets
Key Responsibilities:
- Prepare and submit Drug Master Files (DMFs) and Certificates of Suitability (CEPs) for global markets (US, EU, etc.)
- Ensure compliance with regulatory guidelines (USFDA, EMA, WHO)
- Coordinate with R&D and QA for dossier compilation
- Respond to regulatory queries and maintain documentation
Required Skills:
- Expertise in DMF/CEP filing and global regulatory requirements
- Familiarity with eCTD submission processes
- Strong analytical and communication skills
- Open Positions: Multiple
5. Oral Solid Dosage (OSD) – Formulation & Development (F&D)
- Positions: Executive / Senior Executive
- Qualification: Ph.D. + M.Pharm (Pharmaceutics)
- Experience: 2–7 years
Key Responsibilities:
- Develop formulations for oral solid dosage forms (tablets, capsules)
- Conduct pre-formulation studies and scale-up trials
- Optimize formulations for stability, bioavailability, and manufacturability
- Ensure compliance with cGMP and regulatory standards
Required Skills:
- Expertise in OSD formulation development
- Knowledge of excipients, granulation, and coating techniques
- Familiarity with scale-up and technology transfer
- Open Positions: Multiple
6. Injectable (Injection) – Formulation & Development (F&D)
- Positions: Research Associate / Research Scientist
- Qualification: M.Pharm / Ph.D.
- Experience: 2–5 years in injectable dosage development and lyophilized product development
Key Responsibilities:
- Develop injectable formulations, including lyophilized products
- Perform formulation optimization and stability studies
- Conduct aseptic process development and filter validation
- Document protocols and support technology transfer
Required Skills:
- Experience with injectable and lyophilized product development
- Knowledge of aseptic processing and cGMP
- Familiarity with regulatory requirements for injectables
- Open Positions: Multiple
How to Apply
- Walk-In: Attend the interview at IRM House, Chimanlal Girdharlal Rd, Mithakhali, Navrangpura, Ahmedabad on April 27, 2025, with all required documents.
- Email Application: If unable to attend, send your CV to shardulsinh.k@cadilapharma.com with the subject line indicating the department and position.
- Note: Immediate joiners are preferred. Ensure all documents are complete to streamline the process.
Application Deadline
Walk-in interviews are scheduled for April 27, 2025. Email applications are accepted on a rolling basis.
Contact Us
- Email: shardulsinh.k@cadilapharma.com
- Phone: +91 958-615-7671
- Website: www.cadilapharma.com
Additional Information
- Location Context: Chimanlal Girdharlal Road (C.G. Road) is a major commercial hub in Ahmedabad, ranked as the city’s costliest retail location, ensuring easy access to the venue.
- Company Background: Cadila Pharmaceuticals operates USFDA-certified facilities in Dholka and Ankleshwar, with a dedicated R&D center in Dholka employing over 300 scientists. The company is known for innovations like the world’s first boosted-Rifampicin (Risorine) and quadrivalent influenza vaccine (Cadiflu Tetra).
- Employee Feedback: While Cadila offers a learning-oriented environment and good infrastructure, some reviews highlight challenges with work culture and job security, suggesting candidates clarify expectations during the interview.
Join Cadila Pharmaceuticals and be part of a legacy of innovation and care that impacts lives globally. We look forward to meeting you at the walk-in drive! 🌍