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- Tasks: Support QC lab equipment and ensure compliance with industry standards.
- Company: Leading pharmaceutical company focused on quality and innovation.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Opportunity for career growth in a fast-paced, collaborative setting.
- Why this job: Join a dynamic team and make a real impact on drug quality and safety.
- Qualifications: Experience in QC equipment management and strong problem-solving skills.
The predicted salary is between 45000 - 55000 £ per year.
This role is responsible for supporting all Quality Control (QC) laboratory equipment and associated electronic systems throughout their full lifecycle. The position supports technical developments within the QC laboratory environment and oversees third-party contractors to ensure operations are conducted in line with internal procedures, current Good Manufacturing Practice (cGMP), and applicable regulatory expectations. The role ensures that QC laboratory systems and software used to support the manufacture, testing, packaging, storage, and distribution of marketed drug products remain compliant with GMP, data integrity, and corporate quality requirements.
Key Responsibilities
- Support and deliver qualification and validation of QC equipment, processes, and electronic systems in line with internal procedures, GMP, and GAMP guidelines.
- Provide input into the drafting, review, and approval of quality policies, systems, and procedures related to QC equipment and systems.
- Ensure QC laboratory systems and software remain in a qualified and compliant state.
- Act as a strong advocate for data integrity principles across all systems and equipment.
- Support procurement of new laboratory equipment and software, including forecasting for replacements and upgrades.
- Coordinate and lead equipment servicing, calibration, repair, and maintenance activities.
- Manage relationships with external vendors and service providers, including technical support and helpdesk services.
- Coordinate vendor site visits, raise purchase orders, and ensure accurate traceability of equipment documentation (e.g. service reports, calibration certificates).
- Support ongoing operation, maintenance, and improvement of manual and electronic systems.
- Coordinate with internal IT teams to ensure systems align with corporate IT and quality policies.
- Manage system updates and upgrades, ensuring continued qualification.
- Ensure procedures are in place and followed for data backup, archiving, retrieval, and access management.
- Lead and manage QC equipment and software projects internally.
- Support and raise change controls to ensure qualification and validation requirements are addressed.
- Maintain equipment and project trackers to ensure visibility, scheduling, and compliance.
- Support review and approval of commercial off-the-shelf (COTS) documentation.
- Provide technical support and troubleshooting for QC analysts and system users.
- Prepare and update SOPs and training materials related to equipment and systems.
- Support investigations related to equipment issues, deviations, CAPAs, and incidents.
- Complete maintenance and work orders in a timely manner.
- Communicate equipment-related updates clearly to all stakeholders.
- Ensure all activities are performed in line with GMP, GDP, internal quality systems, and industry standards.
- Maintain a safe working environment and report incidents and near-misses in line with procedures.
- Ensure product quality through adherence to approved processes and documentation.
- Identify opportunities for continuous improvement, efficiency, and innovation.
- Maintain strong communication with internal stakeholders and external partners.
- Perform duties in line with role objectives, behaviours, and competencies.
QC Senior Equipment Technical Specialist - MAT Cover employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Senior Equipment Technical Specialist - MAT Cover
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Understand their values and how your skills align with their needs. Practise common interview questions and be ready to showcase your expertise in QC equipment and compliance.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from the interview to show your genuine interest in the role.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities that might just be perfect for you. Plus, it’s a great way to ensure your application gets seen by the right people.
We think you need these skills to ace QC Senior Equipment Technical Specialist - MAT Cover
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QC Senior Equipment Technical Specialist role. Highlight relevant experience with QC equipment, validation processes, and any technical support you've provided in previous roles. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality control and how your background makes you a perfect fit for this position. Don’t forget to mention your understanding of GMP and data integrity principles – we love that stuff!
Showcase Your Problem-Solving Skills: In your application, be sure to include examples of how you've tackled challenges in QC environments. Whether it's troubleshooting equipment issues or managing vendor relationships, we want to know how you’ve made a difference in your past roles.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Equipment Inside Out
Make sure you’re well-versed in the QC laboratory equipment and electronic systems mentioned in the job description. Brush up on your knowledge of qualification, validation processes, and GMP guidelines. Being able to discuss specific examples from your past experience will show that you’re not just familiar with the theory but have practical insights too.
✨Showcase Your Project Management Skills
This role involves managing relationships with vendors and coordinating various activities. Be prepared to share examples of how you've successfully led projects or managed external contractors in the past. Highlight your organisational skills and ability to keep everything compliant and on track.
✨Emphasise Data Integrity
Data integrity is a key focus for this position. Be ready to discuss your understanding of data integrity principles and how you’ve applied them in previous roles. Mention any specific experiences where you ensured compliance with data management practices, as this will resonate well with the interviewers.
✨Prepare Questions About Continuous Improvement
The job mentions identifying opportunities for continuous improvement. Prepare thoughtful questions about the company’s current processes and how they approach innovation. This shows your proactive mindset and genuine interest in contributing to their goals, making you stand out as a candidate.