Job Title: Global Quality & Regulatory Operations Quality - Quality Partner
Who We Are
Join us in our mission to transform patients' lives! Our client is at the forefront of the pharmaceutical industry, driven by a commitment to scientific rigour and ethical practises. Quality is not just a goal; it is a competitive advantage that allows us to deliver high-quality products while fostering continuous improvement and innovation.
Role Purpose
As a Quality Partner, you will play a pivotal role in ensuring compliance and operational excellence through effective document management. You will facilitate the migration of our document management system and develop retention time policies that align with our organisational needs.
Key Responsibilities:
* Drive business results and enhance customer value through effective document workflows.
* Author and review documents, performing technical reviews in collaboration with your manager.
* Coach and mentor less experienced quality professionals, providing guidance and support.
* Prepare documentation for audits, ensuring compliance with regulatory standards.
* Identify issues proactively and provide solutions, communicating significant quality concerns to Executive Management.
Your Impact:
* Work independently with minimal supervision to complete daily tasks and make informed decisions.
* Implement process improvements to drive innovation within your area of influence.
* Foster strong partnerships across departments, championing a culture of continuous improvement.
What You Bring:
* 2+ years of relevant experience in Quality and Regulatory Operations.
* Bachelor's or Master's degree in Life Science, Data Science, or a related field, or equivalent experience.
* Completed training as a technician or laboratory technician, or possess an equivalent qualification.
* A proactive problem-solver with a passion for innovation and process improvement.
Additional Information:
* This is a full-time, fixed-term contract for 6 months.
* Driving is required, as travel to other sites in the Stirling area will be necessary.
* International business travel may also be required based on project activities.
Location:
Primarily based at Eurocentral, Lanarkshire (Scotland), with potential flexibility under extraordinary circumstances.
Why Join Us?
Be part of a dynamic and diverse team where your contributions matter! Our client is committed to creating an inclusive workplace that embraces a range of backgrounds and perspectives. We are looking for enthusiastic individuals who are ready to innovate and make a difference in the lives of patients.
Ready to Make an Impact?
If you are excited about quality, compliance, and making a difference in the pharmaceutical industry, we would love to hear from you! Apply now to join a team that is dedicated to excellence and driven by purpose.
Equal Opportunity:
Our client is an equal opportunity employer, and we welcome applications from all individuals regardless of background or experience.
Let's create a brighter future together!
Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.