Explore Research Associate & Senior Research Associate jobs in ARL Documentation at Cadila Pharmaceuticals, Dholka Plant. 1–5 years of experience required. Apply now to work with a globally renowned pharmaceutical leader in a GLP-compliant environment.
💼 Cadila Pharmaceuticals Research Associate/Sr. Research Associate – ARL (Documentation) | Apply Now
Are you an experienced professional in pharmaceutical documentation and analytical research? Cadila Pharmaceuticals is hiring for the role of Research Associate / Senior Research Associate – ARL (Documentation) at its state-of-the-art manufacturing facility in Dholka, Gujarat.
This is an exciting opportunity for talented professionals with 1–5 years of experience in analytical R&D, regulatory documentation, and GLP compliance to grow within one of India’s leading pharmaceutical companies.
📍 Job Location:
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Dholka Plant, Cadila Pharmaceuticals, Gujarat, India
🏢 Department:
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ARL – Documentation (Analytical Research Laboratory)
🎓 Designation:
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Research Associate / Senior Research Associate
🕒 Experience Required:
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Minimum: 1 Year
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Maximum: 5 Years
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Ideal for candidates with hands-on experience in analytical instruments, SOP writing, compliance monitoring, and regulatory documentation.
🧪 Key Responsibilities:
As a member of the ARL Documentation team, you will play a vital role in supporting regulatory submissions and ensuring documentation integrity in a GLP-compliant setting.
Your Role Will Include:
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✅ Ensuring GLP (Good Laboratory Practice) compliance according to Indian and international regulatory standards
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✅ Maintaining reference standards, working standards, and impurity standards documentation
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✅ Issuing and monitoring HPLC column records
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✅ Performing calibration of laboratory instruments, such as:
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HPLC
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Dissolution Apparatus
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UV-Vis Spectrophotometer
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FTIR
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GC
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LC-MS/MS
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Auto Titrators
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Analytical Balances
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✅ Daily calibration and monitoring of:
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pH meters
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Refrigerators
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Thermometers
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Other essential lab equipment
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✅ Drafting, reviewing, and revising SOPs for the Analytical Lab
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✅ Maintaining Laboratory Notebook (LNB) and Method Reconciliation Sheets (MRS) for validation and development batches
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✅ Generating indents for lab requirements such as chemicals, solvents, spare parts, columns, and standards
📋 Key Requirements:
To qualify for this role, candidates must meet the following criteria:
✅ Educational Background:
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B.Sc / M.Sc in Chemistry or Life Sciences
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B.Pharm / M.Pharm in Pharmaceutical Sciences
✅ Technical Skills & Experience:
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1–5 years of relevant experience in the pharmaceutical industry
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Strong understanding of analytical method validation, calibration, and documentation
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Knowledge of 21 CFR Part 11 compliance and data integrity principles
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Expertise in preparing and maintaining SOPs, instrument logs, and GLP records
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Experience with HPLC, GC, FTIR, UV-Vis, LC-MS/MS and other analytical platforms
✅ Soft Skills:
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Excellent attention to detail
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Proficiency in written and spoken English
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Ability to work independently and as part of a team
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Organizational and time-management skills
🌟 Why Join Cadila Pharmaceuticals?
Cadila Pharmaceuticals is not just a workplace—it’s a platform for growth, learning, and innovation.
What We Offer:
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🧬 Opportunity to work in world-class R&D and manufacturing facilities
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💼 Exposure to global regulatory standards (USFDA, MHRA, WHO-GMP)
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📈 Career progression and internal promotions
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💸 Competitive compensation packages
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👩🔬 A professional environment rooted in scientific excellence
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🌐 Work with cross-functional teams on international filings & regulatory submissions
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🎓 Training & development opportunities for upskilling
📧 How to Apply:
Interested and qualified candidates may share their updated resume with the HR department at:
📩 Email: drashti.chaudhari@cadilapharma.com
Make sure to include:
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Updated CV
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Cover letter (optional but recommended)
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Subject: Application for Research Associate/Sr. Research Associate – ARL (Documentation)
🧬 About Cadila Pharmaceuticals:
Founded in 1951, Cadila Pharmaceuticals Ltd. is one of India’s oldest and most trusted pharmaceutical companies. With over 70 years of excellence in research, manufacturing, and export, the company delivers high-quality, affordable healthcare solutions globally.
Cadila has a presence in more than 100 countries, with a strong focus on:
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Therapeutic innovation
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Regulatory compliance
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Technology-driven formulations
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Global partnerships with R&D organizations
⚠️ Disclaimer:
Cadila Pharmaceuticals is an equal opportunity employer. All recruitment decisions are based on qualification, merit, and business needs. We do not discriminate on the basis of race, gender, religion, nationality, disability, or any other legally protected status.
📌 This position at Cadila Pharmaceuticals is perfect for candidates aiming to build a long-term career in pharmaceutical documentation, compliance, and analytical R&D. You will get the opportunity to be part of high-impact projects and contribute to life-saving medicines while developing professionally.
Don’t miss this chance to advance your career with one of India’s top pharmaceutical companies!
➡️ Apply today and take the next step toward a rewarding career in pharma research and documentation.
