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Enter your email to apply Requisition ID : SUP001430
MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products.
The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where MSD has codified its 125-
year legacy. MSD’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
MSD Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide.
Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.
Responsible for end to end planning across site including management of the receipt, planning and release of Drug Substance and ensuring the timely release of Drug Product.
Work closely with Quality / Micro Labs to establish a rhythm wheel for sample testing that will support steady state activities on the Vial / Syringe lines.
Ensure that objectives are effectively achieved, consistent with MSD’s requirements to ensure compliance, safety and reliable supply to our customers.
Review of new material introduction and change notifications as they relate to production planning. Work closely with QC to develop a rhythm wheel for incoming testing, TOC and conductivity testing.
Play a key role in developing and maintaining a lab capacity model for QC. Work closely with QA to plan the timely receipt and release Drug Substance.
Work with QA Team to ensure batches release as per LROT to meet customer needs. Liaising with warehouse to develop and maintain the shipping report for site products to ensure consistent and steady supply to downstream sites.
Work closely with the site finite planners to ensure any schedule delays are reflected in end to end plan.
Management of component sales order processing and execution to committed customer ships dates. Liaising with offsite network planners to ensure firmed purchase order accuracy for product shipment.
Creation of shipping schedule for QC samples (stability, ICP, Tailgates, ID testing, release testing and chemistry testing).
Ensure accurate and reliable plan issued weekly for quality equipment including isolators, incubators and analysers.
Required to comply with MSD Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
Work collaboratively to drive a safe and compliant culture in Carlow.
Perform other duties as assigned. Qualifications
Skills and Knowledge
Your role at MSD is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement.
At MSD, we’re inventing for life.
MSD is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails.
All resumes submitted by search firms to any employee at MSD via email, the Internet or in any form and / or method without a valid written search agreement in place for this position will be deemed the sole property of MSD.
No fee will be paid in the event the candidate is hired by MSD as a result of the referral or through other means.