Now Hiring at Neuland Laboratories – QA Roles for Experienced Professionals!

Neuland Laboratories is expanding its team and is currently hiring skilled professionals in the Quality Assurance department. If you have 4–5 years of experience in QA and are looking for a dynamic workplace to grow your career, this could be your chance!

📍 Job Location:

Unit-2, Pashamylaram, Sangareddy

🧪 Department:

Quality Assurance

🧑‍🎓 Qualifications Required:

• B.Pharmacy

• M.Sc

🕒 Experience:

4–5 Years

📌 Open Positions:

1. Investigation (QA)

2. In-Process Quality Assurance (IPQA)

🔧 Key Responsibilities:

🔍 Investigation (QA):

• Managing Deviations, OOS, OOT, Incidents & Change Controls

• Conducting Root Cause Analysis (RCA) and implementing CAPA

• Preparing timely reports and ensuring closure

• Assisting during internal & external audits

🧾 In-Process Quality Assurance (IPQA):

• Performing line clearance, in-process checks, and BMR reviews

• Monitoring GMP compliance across production & packing areas

• Ensuring documentation accuracy and adherence

• Verifying equipment before use

📧 How to Apply:

Interested candidates can send their CVs to:
📩 ksoni@neulandlabs.com

🔖 Tags:

#WeAreHiring #QualityAssurance #NeulandLabs #Investigation #IPQA #PharmaCareers

Stay tuned to our blog for more job opportunities in the pharmaceutical sector. If this job suits your profile or someone in your network, don’t hesitate to share!

New Opportunity: Deputy Manager – Quality Control (Stability) at Neuland Laboratories 

Are you an experienced pharmaceutical professional looking for your next big opportunity in Quality Control? Here's an exciting opening that could be the next step in your career!

🔍 Position: Deputy Manager – Quality Control (Stability)
🏢 Company: Neuland Laboratories Limited
📍 Location: Unit-2, Pashamylaram, Sangareddy
🧪 Experience Required: 12–14 years
🎓 Qualifications: M.Sc / B.Pharmacy / M.Pharmacy

🔧 Key Responsibilities:

• Proficient in handling and troubleshooting HPLC (Empower software)

• Practical knowledge of LIMS and Caliber systems

• Maintenance and operation of Stability Chambers

• Experience in managing regulatory queries related to stability

• Leading a team of 15–20 quality control professionals

This role is a great fit for seasoned professionals in QC Stability who are ready to lead and make a significant impact in a leading API manufacturing organization.

📧 How to Apply:

If you meet the qualifications and have relevant experience, don’t miss this opportunity!
Send your updated CV to 👉 ksoni@neulandlabs.com

📢 Help Spread the Word:

If you know someone who fits this role, please share this post within your network. Let’s help connect the right talent to the right opportunity.

Role: Scientist – API Process R&D at Cipla (Vikhroli, Mumbai)

📍 Location & Company

Cipla, a globally recognized pharmaceutical leader, is hiring for an API Process R&D Scientist at their Vikhroli, Mumbai facility. This strategic role is ideal for candidates with 3–5 years of experience and an M.Sc. in Organic Chemistry aimed at optimizing and innovating active pharmaceutical ingredient (API) processes 

🧪 Role Overview

As a Scientist in API Process R&D, you will:

• Conduct extensive literature surveys to identify and assess synthetic routes.

• Design and execute lab-scale development strategies, including QbD (Quality by Design) studies.

• Optimize process parameters and scale-up to pilot production batches.

• Prepare detailed documentation (e.g., development reports, solubility profiles, impurity data).

• Collaborate with manufacturing teams to support technology transfer 

🎯 Ideal Candidate Profile

• Qualification: M.Sc. in Organic Chemistry.

• Experience: 3–5 years in process R&D, especially in API development.

• Key Skills:

  • Strong grasp of synthetic chemistry and scaling methodologies.

  • Familiarity with QbD frameworks and regulatory best practices.

  • Proficiency in documentation and scientific reporting.

  • Team-oriented approach with strong problem-solving capabilities 

🚀 Why This Role Matters

• Global Impact: Join a company committed to cost-effective, life-saving medicines across 80+ countries 

• Innovative Work: Play a central role in shaping novel API ramp-up strategies and enhancing production efficacy.

• Career Growth: Accelerate your trajectory within Cipla's robust R&D ecosystem, working on cutting-edge technologies.

• Collaborative Environment: Engage with multidisciplinary teams in research, development, and manufacturing.

✅ How to Apply & Prepare

1. Update Your Resume
   Emphasize your experience in API synthesis, QbD studies, and scale-up projects.

2. Gather Supporting Documents
   Include publications, patents, or internal reports showcasing process optimizations.

3. Prep for Technical Interviews
   Be ready to discuss:

   • Route selection criteria and alternative pathways.

   • Case studies involving QbD implementation or impurity reduction.

   • Challenges faced during scale-up and technology transfer scenarios.

4. Showcase Soft Skills
   Demonstrate collaborative thinking, compliance awareness, and documentation rigor.

💡 Pro Tips

• Highlight prior QbD or impurity profiling work, showcasing regulatory alignment.

• Mention any process improvements that led to cost savings or yield enhancement.

• Explain your experience in lab-to-pilot scale transitions—always a key point in this role.

Final Thoughts

If you’re an Organic Chemistry graduate with a few years of hands-on experience, this opportunity at Cipla’s Vikhroli R&D center is a gateway to impactful career growth. You’ll be instrumental in developing essential APIs that improve patient lives globally. Need help refining your resume, prepping for a technical interview, or organizing your scientific portfolio? I’m here to help! 😊

Job: Pharmacovigilance Specialist – TCS (Mumbai)

📅 Walk-In Interview Details

• Date: May 24, 2025

• Time: 10 AM – 1 PM

• Venue: TCS Ltd, Olympus, Security Block, 1st Floor, Hiranandani Estate, Thane West, Mumbai 

• Eligibility: B.Pharm/M.Pharm with 1–5 years of experience in pharmacovigilance, case processing, or ICSR handling 

🔍 Company & Role Overview

TCS is a global IT and consulting powerhouse, but it also leads in life sciences, offering robust Pharma and Drug Safety careers in Mumbai. The Pharmacovigilance Specialist position offers hands-on work in adverse event analysis, regulatory compliance, and global safety processes. 

🛠️ Key Responsibilities

• Process and assess Individual Case Safety Reports (ICSRs) with thoroughness and regulatory insight.

• Manage drug safety databases (like ARGUS/ARISG) effectively.

• Coordinate with healthcare professionals for accurate adverse event documentation.

• Ensure strict adherence to global pharmacovigilance regulations. 

🎯 Ideal Candidate Profile

• Qualifications: B.Pharm or M.Pharm

• Experience: 1–5 years in PV, especially ICSR management and drug safety databases

• Skills: Proficiency with ARGUS/ARISG, strong communication, attention to detail, and regulatory understanding 

💰 Compensation & Perks

• Competitive package in the range of ₹4–8 LPA, with benefits and growth potential.

• Structured career path with training, cross-functional exposure, and global mobility. 

✅ Why This Role Shines

• Brand Strength: Working with a globally trusted name in life sciences consulting.

• Growing Field: PV professionals are in high demand within India and globally.

• Career Advancement: Offers potential movement into roles like Medical Reviewer, RIM Specialist, or Clinical Safety Manager.

📝 How to Apply & Prepare

1. Documents to carry: Updated resume, government ID, passport photo, experience certificates 

2. Resume focus: Showcase ICSR processing, database management (ARGUS/ARISG), and regulatory compliance

3. Interview prep: Review pharmacovigilance workflow, database tools, and examples of adverse event handling

4. Be punctual: Arrive early on May 24 with complete documents

💡 Insider Tip

From a reddit user insight:

“TCS is hiring B.Pharm graduating batch of 2025 for Pharmacovigilance… This is a great opportunity anyone graduating B.Pharm in 2025 must definitely go.” 
Even fresher-qualified candidates were encouraged to attend previous PV hiring drives—so if you're recent or have minimal experience, this is a golden chance.

🚀 Final Take

If you're a B.Pharm/M.Pharm professional with PV experience—or even a fresher stepping into the field—this walk-in by TCS on May 24, 2025 is a strategic move. With its global exposure and structured career roadmap, it’s a strong launchpad into pharmacovigilance. Let me know if you’d like help crafting your PV-focused resume, prepping for case-study interviews, or getting insights into ARGUS/ARISG tools! 😊

Featured Opportunity: Pharmacopoeial Associate – Indian Pharmacopoeia Commission (Ghaziabad)

📅 Walk‑in Interview Details

• Date: 17 July 2025

• Time: 9 AM–10 AM (report early — latecomers won’t be entertained) 

• Location: IPC headquarters, Ghaziabad (Ministry of Health & Family Welfare autonomous body)

💼 Role Overview: Pharmacopoeial Associate & Senior Associate

🔹 Pharmacopoeial Associate

• Monthly Salary: ₹35,000

• Education: Master’s in Pharmacology / Clinical Pharmacology / Pharmacy Practice / Clinical Research / Pharm.D / MBBS / BDS

• Experience: 0–1 year in clinical research

🔹 Senior Pharmacopoeial Associate

• Monthly Salary: ₹45,000

• Education: Same as above

• Experience: Minimum 4 years in clinical research 

🧩 What You’ll Be Doing

• Analytical Review: Assess submitted pharmacopeial documents and ensure compliance with Indian pharmacopoeia standards.

• Documentation & Testing Oversight: Manage pharmacopoeial testing workflows and liaise with labs to ensure quality standards.

• Report Generation: Compile detailed reports on sample analyses and deviations.

• Compliance Adherence: Follow SOPs, maintain regulatory records, and assist senior staff.
  (Note: Exact responsibilities inferred from typical IPC Associate role.)

🔎 Who Should Apply?

• Educational Background: Advanced degree (MPharm, PharmD, MBBS, BDS) in pharmacy or clinical sciences.

• Experience: Freshers are welcome for the Associate role; those with ≥4 years clinical research exposure are fit for the Senior position.

• Skills: Detail-oriented mindset, strong documentation and communication skills, familiarity with lab and regulatory environments.

• Location: Willingness to relocate to Ghaziabad; all educational documents needed on interview day. 

📝 How to Prepare

1. Application Package:

   • Bring originals + self-attested copies of degrees, experience certificates, and a passport-size photo. 

2. Resume Enhancement:

   • Highlight relevant lab methodology, clinical research projects, and report writing.

3. Interview Prep:

   • Brush up on pharmacopoeial standards (e.g., Indian Ph. monographs), clinical trial data handling, and compliance frameworks.

4. Be Punctual:

   • Arrive between 9–10 AM on 17 July — don't be late. 

🚀 Why This Role Stands Out

• Reputed Organization: Work with India’s premier standards-setting body — IPC sets benchmarks for medicine quality.

• Career Stepping Stone: One-year contract but with high potential for future roles in regulatory affairs, quality control, and R&D.

• Hands-on Experience: Gain real-world exposure to pharmacopoeial standards, analytical testing, and compliance frameworks.

• Transparent Pay: Competitive, clearly defined salary for both levels.

✅ Final Take

If you're looking to kickstart or accelerate a career in pharmaceutical standards, testing, or regulatory affairs, IPC’s walk-in for Pharmacopoeial (Senior) Associate on 17 July 2025 is a golden opportunity. Prepare thoroughly, bring your documents, and be ready to shine in Ghaziabad — it could be the first leap in a fulfilling pharma career.