Cookie NoticeManufacturing Shift Lead page is loaded## Manufacturing Shift Leadlocations: Dublintime type: Full timeposted on: Posted Todayjob requisition id: R-*******Title:**Manufacturing Shift Lead**Company:**Ipsen Manufacturing Ireland Ltd**About Ipsen:**Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience.
Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.
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**Job Description:**Ipsen in Ireland is represented by a dynamic state-of-the-art manufacturing facility dedicated to producing Active Pharmaceutical Ingredients (API's) for our core product portfolio.Due to business demands and capacity increase requirement, we are seeking a proactive and driven **Weekend Manufacturing Shift Lead** to join our Blanchardstown site, working **3 x 12 hr. shift premium – 38.5h in a three-week cycle (no nights).
**In this key position, you will ensure the smooth execution of GMP-compliant processes, support site-wide production targets, and help maintain continuous manufacturing operations.
This position is offered on 18-month fixed-term position with a 25% weekend shift allowance.
Successful applicants should be ready to start a training program beginning in January ****.
The program will run alongside the current downstream team - (4 Day working week Mon – Thurs & Tues – Fri) with the first working weekend commencing on March 27th, ****.**About the role:**This weekend shift position plays a key role in maintaining continuous manufacturing operations and supporting overall site production throughput.
As a member of the dedicated weekend team, you will lead the seamless execution of GMP-compliant processes across multiple manufacturing platforms.Lead the efficient execution of the production plan within Manufacturing in line with budgetary plan timelines laid out by the Manufacturing Manager.
Working within a regulatory environment, you will support both upstream and downstream processing activities and receive cross-functional training across Synthesis, Purification, and Cleanroom operations.Participate in structured training across both downstream and upstream operations, scheduled according to the current downstream work pattern (4 Day working week Mon – Thurs & Tues – Fri).
**Key Responsibilities:*** Managing manufacturing shift operations ensuring that all manufacturing operations are completed to schedule.
* Lead the efficient execution of the manufacturing plan in line with budgetary plan timelines laid out by the Manufacturing Manager.
* Provide timely visibility through tier meetings and visual management on progress against value stream KPIs, delays, action plans, improvement opportunities and recognition.
* Ensure objectives are aligned, integrated across the shift team,* Execute daily production operations as directed by Manufacturing Manager, ensuring productivity, timeliness, and cost-efficiency while adhering to GMP and EHS standards.
* Management of supply requirements to meet Ipsen SFG & API requirements in accordance with the annual production plan.
* Support the Manufacturing Manager in ensuring the Manufacturing Technologists and Senior Manufacturing Technologists are trained appropriately and identify gaps in the training matrices.
* Support upstream and downstream manufacturing activities, including synthesis, purification, and lyophilisation.
* Set up, operate, calibrate, and troubleshoot manufacturing equipment.
* Complete batch record documentation and in-process checks in compliance with GMP, ensuring timely submission to Quality.
* Maintain high standards of housekeeping and cleanliness in all work areas.
* Rotate across functional areas (Synthesis, Purification, Cleanroom) to support production schedules and site priorities.
* Liaise effectively with cross-functional departments to ensure smooth operations.
**Work Pattern:** Three -week cycle on rotation**Week 1:**Friday: Rest daySaturday, Sunday, Monday: 07:*******:00**Week 2:**Friday: Rest daySaturday, Sunday, Monday: 07:*******:00**Week 3:**Friday: 07:*******:30Saturday, Sunday, Monday : 07:*******:00**Qualifications & Experience****Minimum:*** 2+ years relevant work experience within an GMP manufacturing environment in an expert capacity* Working knowledge of cGMP, EHS, and operational excellence principles.
* Ability to work both independently and collaboratively in a fast-paced, regulated environment.
* Demonstrated adaptability and teamwork across functional areas.
* Strong documentation accuracy and communication skills.
**Preferred:*** 5+ years relevant work experience within an GMP manufacturing environment in an expert capacity* Diploma in science related discipline, Ideally BSc.
in science.
* Familiarity with processing equipment, automation systems and peptide manufacturing.
* Experience with MES, SAP, and electronic batch record systems.
* Knowledge of Operational excellence and/or Lean Six Sigma.If you can point to an appropriate qualification and/or relevant experience, we would be delighted to engage with your application.
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