Qc Systems Team Lead

3 months ago

Dundee, United Kingdom Argenta Full time

At Argenta we have a passion for what we do, and we relish a challenge. Are you an experienced Analytical Team Lead looking for a new opportunity?_

So who are Argenta? 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 are the key to our success to date.

Argenta has continued to grow operations across 6 sites with locations in New Zealand, the United States, UK and Europe with over 600 employees globally.

A small restructure within our Quality Control department has led to an opportunity for a Systems Team Lead joining our QC team. Reporting directly to the Quality Control Manager you will be responsible for coordinating equipment qualifications and maintenance, scheduling, planning, compliance and AS&T activities. You will take the lead on QC and AS&T training tasks ensuring team members are onboarded and trained to Argenta standards and methods.

We want you to have a hands on approach already be leading a team or be in a supervisory role. You will be responsible for your teams performance and engagement, provide leadership, coaching and upskilling your team members. You will also take accountability for the performance of your team ensuring that both you and your team have commitment to continuous improvement, and ensure resource is at capacity to meet business needs.

We ask you to:

- Develop and continuously improve Argenta's Laboratory Systems, ensuring lean processes and aligning with regulatory requirements
- Lead, mentor and train analysts, providing technical expertise and support
- Be an ambassador and lead HSE activities
- Drive adequate rolling forecast for the business enabling full visibility of QC activities
- Embrace culture of RFT performance of team
- Ensure all activities are completed within the agreed timelines
- Lead closure to compliance actions, support as needed with LIR closures
- Manage stock control

You will hold:

- A higher qualification in a relevant scientific discipline
- The necessary skills, knowledge and experience in method development, validation and method transfer
- Past experience of being a team leader or supervisor within a pharmaceutical related environment
- Significant experience of working in a cGMP & Global regulatory environment
- A high level of Technical Expertise in Chemistry and laboratory techniques
- Successful track record in laboratory-based troubleshooting
- Advanced knowledge and experience in a cGMP Quality Environment
- Excellent communication skills both written and oral
- Skilled in Microsoft office suite, advanced excel skills
- Ability to work collaboratively, and engage, guide and mentor staff
- Flexibility and ability to multitask and time manage effectively
- Experience with chromatography systems & software is required and associated analytical methods

If this is you, we cannot wait to hear from you

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