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- Tasks: Test materials, maintain lab equipment, and support quality systems.
- Company: Join a leading global pharmaceutical company in Hatfield.
- Benefits: Gain experience in a dynamic environment with potential for growth.
- Why this job: Make an impact in healthcare while developing your skills in quality control.
- Qualifications: Knowledge of Quality Control and GMP is essential; computer skills required.
- Other info: This is a 1-year fixed term contract with opportunities for learning.
The predicted salary is between 36000 - 60000 £ per year.
CK Group are recruiting for a QC Analyst, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a 1 year fixed term contract.
Role: This job is responsible for ensuring that all materials are tested according to agreed specifications and procedures and within agreed lead times.
- To test all materials according to agreed specifications and procedures.
- To qualify all laboratory equipment.
- To maintain and calibrate all laboratory equipment according to approved procedures.
- To maintain all laboratory Quality Systems and Quality Management Systems in compliance according to approved procedures.
- To write under supervision, all SOPs associated with QC support.
- To support the internal and external audit process and audit schedules as appropriate.
- To support the preparation and hosting of competent authority inspections.
- To raise and support the investigation of deviations and associated CAPA’s.
- To support the collection of data for reporting Quality Assurance Performance Indicators.
- To support the implementation and management of stability programmes.
- To perform any other appropriate duties at the request of the QC Head.
Your Background:
- Ability to establish and maintain effective working relationships and communication links within affiliated organisations and other customers.
- Extensive knowledge of Quality Control, Quality Assurance, Quality Systems, GMP, Regulatory Compliance and manufacture and packaging of pharmaceutical products.
- Good technical and scientific judgement.
- Ability to interpret complex data and present key findings.
- Computer literate e.g. Word, Excel and PowerPoint.
- Demonstrated Knowledge, understanding and application of GMP Guidelines and Regulations.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 134 138 in all correspondence.
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst
✨Tip Number 1
Familiarise yourself with the latest GMP guidelines and regulations, as this knowledge is crucial for a QC Analyst role. Being able to discuss specific examples of how you've applied these principles in past experiences can really set you apart during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in quality control. Attend relevant conferences or webinars to make connections and learn about the latest trends and challenges in the field.
✨Tip Number 3
Prepare to demonstrate your technical skills during the interview process. Be ready to discuss specific laboratory equipment you’ve worked with and how you’ve ensured compliance with quality systems in previous roles.
✨Tip Number 4
Showcase your ability to work collaboratively by preparing examples of how you've successfully communicated and built relationships with cross-functional teams. This is key in a QC Analyst role where teamwork is essential.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the key responsibilities and required skills for the QC Analyst position. Tailor your application to highlight how your experience aligns with these requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience in Quality Control, Quality Assurance, and any relevant laboratory work. Use specific examples to demonstrate your knowledge of GMP and regulatory compliance.
Showcase Technical Skills: Make sure to mention your proficiency in using software like Word, Excel, and PowerPoint. If you have experience with laboratory equipment or quality management systems, include that as well.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarises your qualifications but also expresses your enthusiasm for the role and the company. Mention your ability to work collaboratively and support audit processes, as these are key aspects of the job.
How to prepare for a job interview at CK Group
✨Know Your Quality Control Basics
Make sure you brush up on your knowledge of Quality Control, Quality Assurance, and GMP guidelines. Be prepared to discuss how these principles apply to the role and provide examples from your past experience.
✨Demonstrate Technical Proficiency
Since the role requires a good understanding of laboratory equipment and procedures, be ready to talk about your experience with maintaining and calibrating lab equipment. Highlight any specific tools or technologies you've worked with.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills, especially regarding deviations and CAPAs. Think of examples where you've successfully navigated challenges in quality systems or audits.
✨Showcase Your Communication Skills
Effective communication is key in this role. Be prepared to discuss how you've established working relationships in previous positions and how you would approach collaboration with internal and external stakeholders.
