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.
