Pilot Plant Manager | Chemical Pharmaceutical CompanyAbout Our ClientChemical Pharmaceutical Company, located in Lodi area.Job DescriptionThe resource, reporting to the Production Manager, will have the following responsibilities:Leadership and Team ManagementLead and mentor a team of technicians and a team leader working in the Kilo Lab.
Provide technical guidance, training, and support to team members to ensure their professional growth and development.
Foster a collaborative and supportive work environment that promotes innovation and excellence.
Facilitate initiatives for training need identification and building requisite skills competencies through systematic training skill-upgradation initiatives for the team.
Actively drive, in conjunction with the leadership team, the performance management process of the team.
Recognize reward excellent performers affirm key contributions of employees toward the achievement of goals objectives of the team.Kilolab Operations ManagementOversee day-to-day operations of the kilolab facility, including scheduling experiments, resource allocation and optimization, and workflow optimization.
Ensure adherence to Standard Operating Procedures (SOPs), safety protocols, and Good Manufacturing Practices (GMP) to maintain a safe and compliant work environment.
Implement practices for laboratory operations, equipment maintenance, and inventory management to maximize efficiency and productivity.Project ManagementCollaborate with project managers, chemists, and clients to develop project plans, timelines, and deliverables for kilolab activities.
Coordinate with cross-functional teams to ensure alignment of kilolab activities with overall project objectives and timelines.
Monitor project progress, identify potential risks or issues, and implement corrective actions as needed to ensure on-time delivery of high-quality products.Quality Assurance, Regulatory and ComplianceEnsure compliance with regulatory requirements, including FDA regulations, ICH guidelines, and customer specifications.
Implement quality control measures to monitor product quality, purity, and yield throughout the manufacturing process.
Conduct regular inspections and audits to identify areas for improvement and ensure continuous compliance with quality standards.
Work with LODI Site Head on compliances pertaining to Kilo lab.Technical Expertise and Problem-SolvingUtilize your expertise in organic synthesis, process development, and scale-up to troubleshoot technical challenges and optimize reaction conditions.
Collaborate with RD teams to transfer processes from the laboratory to the kilolab scale, ensuring scalability and reproducibility.SafetyEnsure safety at the Kilo lab by following all the SOPs and guidance from the EHS team.
Drive safety culture in the area of responsibility.The Successful ApplicantRelevant degree in Chemistry, Chemical Engineering, or related field with significant experience in pharmaceutical development or manufacturing.
Experience in pharmaceutical development or manufacturing.
Proven experience in kilolab operations, process development, and scale-up in a CDMO or CRO setting.
In-depth knowledge of GMP regulations, quality systems, and regulatory requirements for pharmaceutical manufacturing.
Hands-on experience with analytical techniques, process optimization, and troubleshooting in organic synthesis.What's On OfferGreat opportunity of career.Contact: Marco MorelloQuote job ref: JN-062024-6442581 #J-18808-Ljbffr
