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For Companies At a Glance
- Tasks: Conduct quality control testing and ensure compliance with industry standards.
- Company: Join a leading manufacturing company focused on innovation and quality.
- Benefits: Gain valuable experience, competitive pay, and opportunities for professional growth.
- Why this job: Make a difference in product quality while developing your skills in a dynamic environment.
- Qualifications: Degree in Pharmaceutical Sciences, Chemistry, or related field preferred.
- Other info: Collaborative team culture with a focus on continuous improvement and personal development.
The predicted salary is between 36000 - 60000 £ per year.
This role supports Quality Control raw materials activities within a regulated manufacturing environment. The position focuses on delivering accurate, compliant analytical work to agreed timelines, while maintaining high quality standards and supporting team performance. The role holder will manage their own workload with guidance from senior staff and contribute to continuous improvement and colleague development.
Key Responsibilities
- Perform and document raw material testing in line with GMP and approved procedures.
- Review, enter and verify analytical data generated by self and others, ensuring data integrity.
- Comply with all site safety, quality and environmental requirements.
- Identify and support improvements in GMP compliance, laboratory efficiency and safe working practices.
- Maintain controlled documentation, including raw material specifications and assay records.
- Prepare and issue raw material release documentation for audits and stakeholder requests.
- Provide supplier certification and supporting quality documentation when required.
- Own the raw material specification release process, ensuring accuracy and timeliness.
- Support retain sample reviews and scheduled audits.
- Plan and manage personal workload, escalating risks or delays to QC leadership.
- Support daily coordination activities within the raw materials team when required.
Skills & Experience
- Adaptable, proactive and able to manage changing priorities.
- Willing to support a range of laboratory and quality activities.
- Working knowledge of chemical and/or biochemical analytical techniques.
- Strong data recording, documentation and quality record management skills.
- Consistently delivers high-quality work to agreed timelines.
- Able to work independently and collaboratively within a team.
- Capable of reviewing others’ work to ensure quality standards are met.
- Maintains confidentiality and acts with professionalism at all times.
- Supportive team member, contributing to training and development of junior colleagues.
Education
- BSc or equivalent in Pharmaceutical Sciences, Chemistry or a related discipline preferred.
Quality Control in Slough employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control in Slough
✨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 a Quality Control role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and analytical techniques. Be ready to discuss how you’ve maintained high-quality standards in past roles. We want to see your passion for quality control shine through!
✨Tip Number 3
Showcase your adaptability! In the fast-paced world of Quality Control, being able to manage changing priorities is key. Share examples of how you've successfully navigated challenges in previous positions.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Quality Control in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience mentioned in the job description. Highlight your knowledge of GMP and any relevant analytical techniques you've used. We want to see how you fit into our Quality Control team!
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 aligns with our needs. Don’t forget to mention your adaptability and teamwork skills – we love a supportive colleague!
Showcase Your Attention to Detail: In a role focused on compliance and accuracy, demonstrating your attention to detail is key. Include examples of how you've maintained high-quality standards in previous roles. We appreciate candidates who can manage their workload while ensuring data integrity!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Planet Pharma
✨Know Your GMP Basics
Make sure you brush up on Good Manufacturing Practices (GMP) before the interview. Understanding how these practices apply to raw material testing will show that you're serious about quality control and compliance.
✨Showcase Your Analytical Skills
Be prepared to discuss your experience with chemical or biochemical analytical techniques. Bring examples of how you've applied these skills in previous roles, especially in relation to data integrity and documentation.
✨Demonstrate Team Spirit
Quality Control is all about collaboration. Think of instances where you've supported your team or contributed to training junior colleagues. Highlighting your adaptability and proactive approach will resonate well with the interviewers.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving abilities in a regulated environment. Prepare scenarios where you've identified improvements in laboratory efficiency or compliance, and be ready to discuss how you managed your workload under pressure.
