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PROCESS TECHNOLOGIST

Descrizione dell'offerta di lavoro

Process Technologist Azienda: Chemical Pharmaceutical Company, located in Lodi area Offerta: The resource, reporting to the Production Manager, will have the following responsibilities: Industrialization of new products into GMP Kilo lab Leadership and Team Management: Lead 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 Management: Oversee 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 Management: Collaborate 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 Compliance: Ensure 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-Solving: Utilize your expertise in organic synthesis, process development, and scale-up to troubleshoot technical challenges and optimize reaction conditions. Collaborate with R&D teams to transfer processes from the laboratory to the kilolab scale, ensuring scalability and reproducibility. Safety: Ensure safety at the Kilo lab by following all the SOPs and guidance from the EHS team. Drive safety culture in the area of responsibility. Strong leadership and team management skills with the ability to inspire and motivate team members. Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and clients. Detail-oriented mindset with a focus on safety, quality, and continuous improvement. Competenze ed esperienza: Relevant degree in Chemistry, 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. Completa l'offerta: Great opportunity of career. #J-18808-Ljbffr
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Dettagli dell'offerta

Azienda
  • Michael Page International Italia Srl
Località
  • Tutta l'Italia
Indirizzo
  • Imprecisato - Imprecisato
Data di pubblicazione
  • 26/12/2024
Data di scadenza
  • 26/03/2025
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