The client is an international pharmaceutical company based in Ireland looking to recruit for an Analytical Development Supervisor. For the role you must have a relevant third level science qualification and strong experience working with PMDIs, DPIs and NGIs and their associated analytical testing methods – cascade Impaction, Dose delivery, Particle Size analysis.
Responsibilities to include:
• Independently plans the best scientific approach to develop analytical methods that meet client requirements. Evaluates available technical options to obtain desired quality of analytical results, economics, ease of introduction into a production environment, and robustness in analytical application. Supervises and oversees method development/optimization/validation projects. Demonstrate viability of in-house developed methods and methods transferred from clients by designing appropriate validation experiments
• Participates in client communications regarding project definitions, technical information exchanges, and discussions of project status. Provides recommendations to clients on technical and regulatory issues.
• Prepare, review and approve bids and proposals, project scope, timelines and pricing. Negotiates with client on timelines and pricing.
• Reviews study protocols, project status reports, final study reports and other project-related technical documents.
• Provides leadership and mentoring to junior level scientists in developing their professional scientific skills. Leads troubleshooting of instrument and analytical problems
• Coordinates laboratory activities of technical staff and prioritizes projects with support functions. Analyzes Partner and timesheet reports for resource planning, revenue projections and recognition, and billing
• Assists in technical sales and marketing, preparation of technical marketing materials. Presents poster and podium presentations at conferences.
Suitable applicants should email their cv to aileen@cpl.ie or call 0035316146007 for a confidential conversation.
