🔬 Piramal Pharma Solutions is a leading global CDMO (Contract Development and Manufacturing Organization) providing advanced drug development and manufacturing solutions to the pharmaceutical industry 🌍💊.
👩 🔬 Role: Analytical Development Scientist
Responsible for analytical method development, validation, and technical transfer.
🧪 Key Roles & Responsibilities
🏢 Departmental Operations:
* ✅ Perform assigned work as agreed with the project lead and/or Analytical Development Manager. Ensure efficient use of time to complete assigned objectives ⏱️.
* 🧼 Maintain laboratory areas in compliance with client, regulatory GMP, and safety requirements 🧯
* 📈 Engage in compliance and continuous improvement projects.
* 🤝 Provide cover for fellow Analytical Development Scientists as required.
* ♻️ Promote economic use of labor, materials, energy, and services. Suggest and implement cost-saving and waste-reduction measures 💡.
* ⚙️ Identify opportunities for improved workflows to enhance efficiency, cost control, and GMP/safety performance.
* 👥 Support onboarding and training of new team members.
📦 Project Delivery:
* 📅 Ensure timely completion of all assigned project deliverables.
* 🚀 Take the lead on project components where appropriate, in agreement with the Analytical Development Manager.
* 🧭 Plan and execute work aligned with project timelines and customer expectations.
* 🧪 Support analytical method development, tech transfer, qualification, and validation activities
* 📋 Coordinate with peers for effective workload planning and timeline adherence.
* ☎️ Communicate with clients professionally as required.
📚 Essential Experience:
* ✅ Minimum 2 years analytical experience.
* 📘 Strong understanding of GMP & SHE standards.
* 🛡️ Solid grasp of safety practices.
* 🤝 Highly developed interpersonal and team-building skills.