Job Description
Join Piramal Pharma Solutions — A Global Leader in Advanced Drug Development & Manufacturing
Are you passionate about scientific excellence and quality in pharmaceutical development? Piramal Pharma Solutions, a leading global Contract Development and Manufacturing Organisation (CDMO), is seeking a dedicated Bio-Assay Scientist to join our innovative team.
About the Role:
As a key member of our Bio-Assay team, you will lead method development, qualification/validation, technical transfer, stability testing, and QC release activities. Your expertise will help ensure our products meet stringent quality and regulatory standards, supporting life-changing medicines worldwide.
Key Responsibilities:
* Prioritise daily tasks aligned with project objectives, guided by senior team members.
* Support routine Bio-Assay QC and stability testing, ensuring all activities follow SOPs, protocols, and cGMP standards.
* Review and verify data in compliance with Data Integrity and regulatory requirements.
* Maintain a compliant, organized laboratory environment that meets client, GMP, safety, and regulatory standards.
* Execute calibration, maintenance, and troubleshooting of laboratory equipment, promptly communicating any issues.
* Provide training and technical support to Development and Quality Control teams.
* Lead compliance and continuous improvement projects, identifying efficiencies and best practices.
* Plan workload effectively to meet project timelines and deliverables.
* Manage deviations, investigations, change controls, and ensure timely resolution and documentation.
* Escalate issues promptly to management to facilitate swift corrective actions.
* Assist in implementing measures and targets across release, stability, development, technical transfer, and validation activities.
* Promote cost-effective practices—optimizing labor, materials, and energy usage.
* Support onboarding and training of new staff members.
* Apply cGMP, Data Integrity, and ESH standards in all activities.
* Contribute to audit readiness and continuous improvement initiatives.
* Support equipment validation activities (IQ/OQ/PQ) and maintain system ownership.
* Draft, review, and update SOPs, protocols, and documentation.
* Identify opportunities for process improvements to enhance efficiency, safety, and GMP compliance.
Qualifications & Skills:
* Proven experience in bioassay method development, validation, and QC release.
* Strong knowledge of cGMP, Data Integrity, and regulatory requirements.
* Excellent organizational, troubleshooting, and communication skills.
* Ability to work independently and collaboratively in a fast-paced environment.
* Experience with equipment calibration, validation, and documentation practices.
Why Join Piramal Pharma Solutions
* Be part of a global organization committed to innovation, quality, and continuous growth.
* Work in a collaborative environment that values your expertise.
* Contribute to impactful projects that improve patient health worldwide.
* Enjoy opportunities for professional development and career progression.
Apply
Join us in advancing healthcare through science and innovation. Submit your application now and become a vital part of Piramal Pharma Solutions.