At Piramal Pharma Solutions, we are driven by a purpose: to help patients around the world live healthier, longer lives. As part of our continued growth, we’re seeking an Analytical Development Scientist to support and lead method development, validation, and technical transfer activities in a dynamic, GMP-compliant environment.
Your Role
You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance.
Key Responsibilities
Project Leadership & Delivery
- Develop, validate, and transfer robust analytical methods for raw materials, intermediates, and finished products.
- Drive timely and compliant execution of project deliverables, ensuring alignment with client expectations.
- Collaborate cross-functionally to plan, schedule, and manage project work across QC, production, and stability teams.
- Participate in client communications and technical discussions, providing expert input and updates as needed.
Technical & Operational Excellence
- Conduct method development and troubleshooting using state-of-the-art instrumentation (e.g., HPLC, GC, UV, etc.).
- Author and review technical documentation including protocols, reports, and SOPs in accordance with cGMP standards.
- Provide analytical expertise during technology transfer to QC and production environments.
- Support analytical training and mentoring for junior staff and cross-functional teams.
Compliance & Continuous Improvement
- Maintain meticulous laboratory records and ensure all work complies with GMP, safety, and data integrity standards.
- Actively contribute to investigations, deviation reports, and change controls.
- Identify opportunities for process optimization, cost reduction, and waste minimisation.
What We’re Looking For
- A degree (BSc/MSc/PhD) in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline.
- Solid experience in analytical method development and validation in a GMP-regulated environment.
- Strong understanding of ICH guidelines and regulatory requirements.
- Hands-on experience with a range of analytical techniques and instrumentation.
- Excellent problem-solving, communication, and project management skills.
Why
- Be part of a global CDMO with a strong reputation in delivering high-quality, end-to-end pharmaceutical solutions.
- Collaborate with passionate scientists and professionals in a supportive, innovation-focused culture.
- Access ongoing training, development, and career advancement opportunities.
- Make a real-world impact in the life sciences industry