Site Head

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title Site Head Job Description The incumbent will be responsible for managing the overall manufacturing operations for the organization involving multiple facilities. The incumbent will guide and lead members of the Operations team to deliver as per the corporate goals, projects, plans and timelines. This position requires demonstrated ability to work effectively as both technical and people leader, manage tasks, resolve problems and issues and drive implementation/action plans to meet objectives along with excellent interpersonal and presentation skills. A person in this role is expected to lead, troubleshoot, incorporate latest systems and processes along with applying innovative thinking to improve effectiveness and efficiency of the function. The incumbent is expected to engage and interact frequently with cross functional teams, senior management, external partners/collaborators, and stakeholders. QUALIFICATION: Postgraduate or PhD degree in a relevant Science or Engineering field EXPERIENCE: • 20 or more years of experience in the GMP manufacturing/operations in vaccines and/or biologics industry • Demonstrated ability to manage entire GMP manufacturing operations with key focus on time bound delivery and quality • Experience in single use/disposable bio process equipment and technologies • Experience with regulatory inspections and inspection readiness • Experience in documentation and compilation of data for regulatory submissions (IND), i.e., transition from product development to commercial quality systems and operations • Thorough understanding and knowledge of global GMP regulations and requirements to support vaccines and biologics manufacturing for human use • Strong team player with demonstrated track record of success in a cross‐functional team and fast moving environment EXPERIENCE: • Excellent organization and planning skills • Strong strat gic thinking and problem solving skills • Ability to take responsibility and ownership along with capability to deliver/execute independently with minimal directions • Ability to integrate complex business considerations in formulating operations efficiency with a quality approach • Excellent cross functional and stakeholder management skills and ability to develop strong relationships across functions, senior leaders, and key stakeholders • Strong communication and interpersonal skills including ability to prepare and deliver effective presentations and provide information to influence major decisions Ability to work with computer controlled systems and proficient with Microsoft Word, Excel, and PowerPoint • Must have a positive attitude and be adaptable to a dynamic “startup” environment without losing focus on business goals Piramal