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QC Scheduler

CK Group- Science, Clinical and Technical
Posted 15 days ago, valid for 14 days
Location

Dundee, City of Dundee DD1 1XA, Scotland

Salary

£25,000 - £35,000 per annum

info
Contract type

Full Time

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Sonic Summary

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  • Position: Quality Control Scheduler
  • Location: Dundee, Angus
  • Salary: Not specified
  • Experience Required: Previous experience in a similar role
  • Qualifications: Degree in Chemistry/Pharmacy/Biology
Quality Control Scheduler
Quality Control Dundee, Angus

An amazing opportunity has arisen for a QC Scheduler, within our Dundee manufacturing site. The successful candidate willbring with them Planner knowledge having held a similar role previously and own the efficient coordination of the schedule demand in line with the departments needs and priorities. You'll be a great team player, building, and driving delivery of the QC Schedule, you will have strong stakeholder management skills with high awareness, confident in your approach to step in when needed to support the site and influence outcomes ensuring that all support activities are aligned to deliver efficient operations. In short you willbuild, manage, and drive delivery of the QC Schedule

Some of what you will do
  • Developing QC testing and training schedules based on production plans, capacity assessments, staff skills, stability requirements, GMP regulations, ongoing projects, and AS&T (Analytical Science and Technology) requirements to meet both GMP and release obligations for QC.
  • Monitoring and reporting progress against schedules, identifying critical risks and potential delays to agreed delivery dates.
  • Collaborating with QC team leaders or managers and Supply Chain to promptly address and mitigate any issues as necessary.
  • Attend and participate in the site Sales and Inventory Operating Planning (SIOP) process
  • Coordinate with other site functions such as Production, Supply chain and other stakeholders to ensure effective communication of QC testing and completion plans and ensure minimal disruptions to operations.
  • Generating reports to ensure we're on track.
  • Maintaining a rolling capacity plan
  • Contributing to refining planning processes and systems by conducting system checks, tests, and developing reports.
  • Ensuring adherence to planning processes and GMP standards and all schedules are accurate, up-to-date, feasible, compliant with GMP regulations, and agreed upon by relevant stakeholders.

Qualifications
  • Higher Education (Degree or equivalent experience) within Chemistry/Pharmacy/Biology

Knowledge/Experience
  • Industry background in pharmaceutical, laboratory or related environment would be advantageous
  • Logistics, materials, planning and planning tools
  • Excellent organisational, planning, administrative, and collaborating skills
  • Ability to set priorities and manage multiple tasks
  • Can deliver to deadlines, with good attention to detail
  • Flexible, self-motivated and collaborative
  • Determination to see jobs through to completion
  • Ability to work as part of a team and on own initiative with multiple teams
  • Strong written and verbal skills

Who are we
At Argenta we have a passion for what we do, and we relish a challenge.

Founded in 2006 by a New Zealand chemist with an entrepreneurial mind, his vision was to touch lives all over the world by the creation, development and production of the best animal health technologies and products. Our vision and our people are unique and is the key to our success to date. Now, Argenta has operations across 6 sites with locations in New Zealand, the United States, UK and Europe with over 600 employees global.

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