Manufacturing Shift Team Leader
PharmaClinical ResearchRegulatory AffairsQuality Assurancegmpcdmcro
Job description
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 Manufacturing Shift Team Leader Job Description The Shift Team Leader is responsible for ensuring the successful execution of the manufacturing process within the manufacturing suite. This includes but is not limited to planning the appropriate resource for the manufacturing process, health and safety of staff, people development and training, quality of product and managing the inter-relationships between Q&V, QC and QA. The aim of this role is to ensure that products are manufactured to schedule in a GMP compliant manner and also to aid the release of those manufactured products. Lead their team of direct reports Management of staff including direction, performance management and feedback, motivation and training Effectively communicate within area of responsibility and across Business Partners and Service Providers Goal Setting, prioritisation, planning, resourcing and review of process performance metrics. Maintain Manufacturing quality and Product Performance to agreed product performance standards Lead deviation investigations ensuring that they a closed in a timely manner. Review draft batch documentation and provide useful insight Compliance to all Health & Safety, Quality and Regulatory requirements. Continuously improve manufacturing operations to deliver gains in either a reduction in cost and time or increase in quality. Define appropriate Training programmes to ensure competency to future business needs Delivering Manufacturing output to Schedule
Stand out for this role
NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Anlagenmechaniker Heizung/Kilma/Lüftung/Sanitär als Gebäudetechniker für das Facility Management (m/w/d)
Eurofins — Hamburg, de
Prácticas - Técnico de laboratorio
Eurofins — Elche Parque Industrial, es
Consultor en Seguridad Alimentaria
Eurofins — Barcelona, es
Auditor Seguridad Alimentaria
Eurofins — Barcelona, es
Assistant(e) Facturation Relance en alternance
Eurofins — Les Ulis, fr
Kimyasal Laboratuvar Analisti
Eurofins — İstanbul, tr