At a Glance
- Tasks: Ensure product quality through inspections, audits, and collaboration with the production team.
- Company: Join Azenta, a forward-thinking company that values innovation and teamwork.
- Benefits: Competitive salary, inclusive culture, and opportunities for personal growth.
- Other info: Dynamic work environment with a focus on continuous improvement.
- Why this job: Make a real difference in product quality and customer satisfaction.
- Qualifications: Experience in quality control and strong organisational skills required.
The predicted salary is between 30000 - 40000 £ per year.
At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships. All we accomplish is grounded in our core values of Customer Focus, Achievement, Accountability, Teamwork, Employee Value and Integrity.
The Senior Quality Inspector is tasked with supporting timely turnaround of products, manufactured and procured. Assisting manufacturing as we strive toward zero defects by conducting audits and random sampling. Working with a quality first mind set where we ensure the customer receives product that exceeds their expectations. Will be the day to day contact for the Quality department.
What You’ll Be Doing:
- Completing part inspection on products produced in house and by sub-contractors
- Measuring parts using calipers, micrometres, CMM
- Creating graphs in excel to enable comparison of QC results
- Updating excel spreadsheets
- Completing inventory transactions in the ERA
- Assisting the production team as required, including completing first off production checks
- Assist with the MRB when necessary
- Raising re-work instructions check the quality of the re-work, occasionally completing re-work
- Working in the biological QC lab running product functional test (experience not required)
- Investigation customer complaints
- Raising & Investigating non-conformance
- Conducting process audits
- Assisting in data reviews and KPI updates
- To assist in maintaining a clean and safe working environment
- Assisting in CAPA and complaint activities as required
- Identify errors and eliminate root cause using robust countermeasures
- Compliance – Support manager to ensure effective internal control structures and procedures are in place, Ensure Audits are completed in all areas, and that any corrective actions are robustly put in place to drive continued improvements
- Tasks related to continuous improvement activities
What You’ll Need:
- Prior experience within Quality control
- Manufacturing within life sciences advantageous
- Strong organizational and time management skills
- Self-motivated, enthusiastic and flexible individual (adapt to differing situations)
- Comfortable working in special conditions as necessary: clean rooms; low humidity; or static – free
- Experience with using CMM is desirable
- Strong work ethic and organizational skills
- Able to multi-task in a fast-paced environment
- Excellent communication skills are essential to the role
If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at Recruiting@azenta.com for assistance. Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status.
QC Supervisor employer: Azenta
At Azenta UK, Ltd., we pride ourselves on fostering a dynamic and innovative work environment where employees are encouraged to challenge the status quo and contribute to our customer-focused culture. Our commitment to employee growth is evident through continuous improvement initiatives and collaborative teamwork, ensuring that every team member feels valued and empowered. Located in a state-of-the-art facility, we offer a unique opportunity to be part of a forward-thinking company dedicated to excellence in quality control within the life sciences sector.
