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- Tasks: Join us as a QC Analyst, testing and approving raw materials in a dynamic pharma environment.
- Company: Be part of a leading pharmaceutical company committed to quality and innovation.
- Benefits: Enjoy a supportive work culture with opportunities for training and career growth.
- Why this job: Make a real impact on product quality while working in a collaborative team atmosphere.
- Qualifications: Ideal for those with analytical skills and a passion for quality control in pharmaceuticals.
- Other info: This is a contract role, perfect for students looking to gain valuable industry experience.
The predicted salary is between 28800 - 43200 £ per year.
This role is responsible for supporting the Quality Control (QC) Raw Materials function within a GMP-regulated environment. The successful candidate will perform a range of testing, documentation, and compliance activities to ensure the quality and suitability of materials for use in manufacturing processes. They will also help maintain high standards of work across the department and support more junior team members.
Key Responsibilities:
- Carry out raw material testing and review data in line with GMP standards and internal procedures.
- Approve and release raw materials for use once specifications are met.
- Support the completion of quality documentation including deviations, CAPAs, investigations, change controls, protocols, reports, and SOPs.
- Review and interpret analytical results, escalating concerns to QC management as needed.
- Approve work and data generated by colleagues, ensuring accuracy and compliance.
- Maintain a safe and compliant working environment by following relevant health and safety procedures.
- Identify and suggest improvements to enhance compliance, efficiency, and safety.
- Manage personal workload and timelines effectively with general guidance.
- Assist in the training and mentoring of junior staff to uphold department standards.
- Promote a culture of quality and continuous improvement within the team.
Required Skills & Experience:
- Ability to work independently on routine tasks, with minimal supervision.
- Demonstrates flexibility and a proactive approach to change and problem-solving.
- Experience with a range of chemical and/or biochemical analytical techniques.
- Skilled in data recording, review, and maintaining quality documentation.
- Strong attention to detail with a focus on quality and compliance.
- Capable of delivering work to deadlines while maintaining high standards.
- Effective team player who supports others and contributes to shared goals.
- Maintains professionalism and discretion when handling sensitive or confidential information.
QC Analyst - Raw Materials employer: Adepto Technical Recruitment Ltd
Contact Detail:
Adepto Technical Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst - Raw Materials
✨Tip Number 1
Familiarise yourself with GMP regulations and quality control processes specific to the pharmaceutical industry. This knowledge will not only help you understand the role better but also demonstrate your commitment to maintaining high standards in your work.
✨Tip Number 2
Highlight any experience you have with chemical or biochemical analytical techniques during your conversations. Being able to discuss specific methods you've used can set you apart from other candidates and show your practical knowledge.
✨Tip Number 3
Prepare to discuss how you've contributed to a culture of quality and continuous improvement in previous roles. Sharing examples of how you've identified issues and suggested improvements can showcase your proactive approach.
✨Tip Number 4
Be ready to talk about your experience in mentoring or training junior staff. This is an important aspect of the role, and demonstrating your ability to support and uplift others can make a strong impression.
We think you need these skills to ace QC Analyst - Raw Materials
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience and skills that align with the QC Analyst role. Emphasise your familiarity with GMP standards, analytical techniques, and any previous roles in quality control or similar environments.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the position and the company. Mention specific experiences that demonstrate your ability to perform raw material testing, manage documentation, and support junior staff, as outlined in the job description.
Highlight Relevant Skills: When detailing your skills, focus on your attention to detail, problem-solving abilities, and experience with compliance and quality documentation. Use examples from past roles to illustrate how you meet these requirements.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your professionalism and attention to detail, which are crucial for a QC Analyst.
How to prepare for a job interview at Adepto Technical Recruitment Ltd
✨Know Your GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) standards, as this role heavily relies on compliance with these regulations. Be prepared to discuss how you have applied these standards in previous roles or how you would approach them in this position.
✨Demonstrate Analytical Skills
Since the job involves reviewing and interpreting analytical results, be ready to showcase your experience with various chemical and biochemical analytical techniques. Bring examples of past projects where you successfully analysed data and made informed decisions based on your findings.
✨Highlight Team Collaboration
This role requires effective teamwork and mentoring of junior staff. Share specific instances where you contributed to team goals or supported colleagues, emphasising your ability to foster a collaborative environment and promote a culture of quality.
✨Showcase Problem-Solving Abilities
The company values flexibility and a proactive approach to problem-solving. Prepare to discuss challenges you've faced in previous roles and how you overcame them, particularly in relation to quality control and compliance issues.
