At a Glance
- Tasks: Conduct laboratory testing and ensure compliance with GMP standards in a dynamic environment.
- Company: Join Planet Pharma, a leading staffing agency recognised for excellence in the pharmaceutical industry.
- Benefits: Gain valuable experience in a regulated lab while working full-time with rotating shifts.
- Other info: Opportunity for growth and learning new analytical techniques in a supportive team.
- Why this job: Make a real impact in quality control and develop your career in pharmaceuticals.
- Qualifications: Degree in Life Science or related field; experience in GMP environments preferred.
The predicted salary is between 30000 - 40000 £ per year.
Location: Dartford, Kent
Contract: 12 Months
Hours: Full Time (40 hours per week)
Shift Pattern: Rotating Early, Late & Night Shifts
Start Date: June 2026
We are seeking a QC Analyst to join a leading pharmaceutical manufacturing environment, supporting quality control activities across laboratory testing, GMP compliance, and production support. This is an excellent opportunity for someone with laboratory experience in a regulated industry who is looking to further develop their career within pharmaceutical quality control.
Key Responsibilities:
- Perform routine laboratory testing in accordance with approved methods, SOPs, and GMP requirements.
- Support testing of raw materials, in-process samples, finished products, and environmental samples.
- Accurately document, review, and report analytical data.
- Assist with laboratory investigations, deviations, CAPAs, and change controls.
- Support cleaning verification activities and sample collection.
- Ensure laboratory equipment is operated, maintained, and calibrated in accordance with procedures.
- Maintain compliance with GMP, data integrity, EHS, and quality standards.
- Participate in shift handovers and communicate results, issues, and priorities effectively.
- Contribute to continuous improvement initiatives within the QC laboratory.
Experience Required:
- Degree in a Life Science, Chemistry, Pharmaceutical Science, Biotechnology, Microbiology, or related discipline.
- Previous experience working within a GMP, GLP, GxP, pharmaceutical, biotech, food, consumer healthcare, or other regulated laboratory environment.
- Experience performing laboratory testing and maintaining GMP documentation.
- Understanding of deviations, CAPAs, investigations, and quality systems.
- Strong attention to detail and commitment to data integrity.
Desirable Experience:
- HPLC, chromatography, FTIR, Raman, particle size analysis, Karl Fischer, microscopy, or other analytical laboratory techniques.
- Environmental monitoring or microbiology testing experience.
- Experience using quality systems such as TrackWise, ComplianceWire, Oracle, or similar platforms.
What We're Looking For:
- Strong organisational and documentation skills.
- Ability to work effectively both independently and within a team.
- Positive attitude and willingness to learn new analytical techniques.
- Comfortable working a rotating shift pattern, including nights.
- Motivated individual with a strong quality and compliance mindset.
If you have experience within a regulated laboratory environment and are looking for your next opportunity within pharmaceutical quality control, we'd be keen to hear from you.
Freelance QC Analyst – GMP Laboratory Environment in Maidstone employer: Planet Pharma
Planet Pharma is an exceptional employer, offering a dynamic work environment in Dartford, Kent, where you can thrive as a Freelance QC Analyst in a leading pharmaceutical manufacturing setting. With a strong commitment to employee growth and development, we provide opportunities for continuous learning and advancement within the regulated laboratory space, all while fostering a culture of collaboration and excellence. Our recognition as one of the top staffing firms by FORBES highlights our dedication to quality and service, making us a rewarding place to build your career.
StudySmarter Expert Advice🤫
We think this is how you could land Freelance QC Analyst – GMP Laboratory Environment in Maidstone
✨Network like a Pro
In the pharmaceutical industry, getting your foot in the door can often come down to who you know. So, connect with professionals through platforms like LinkedIn or attend industry-specific conferences and trade shows. These are golden opportunities to meet decision-makers and to showcase your expertise.
✨Show Off Your Expertise
As a freelancer, you really want to establish yourself as a go-to expert in your niche. Consider setting up a blog or contributing to pharmaceutical forums where you can share insights about trends and innovations. This will help increase your visibility and build credibility in the industry.
✨Join Freelance Platforms
Don't underestimate the power of freelance platforms that focus on the pharmaceutical sector. Websites like Upwork or industry-specific job boards can help you find gigs that match your skill set. Remember to tailor your profile to highlight your relevant experiences and credentials.
✨Leverage Your Local Networks
Since the pharmaceutical industry often hinges on relationships, reaching out to local universities or research institutions can lead to lead generation. They might have collaborations or projects looking for freelance talent. Plus, don’t forget to connect with local pharma associations for gigs and networking opportunities!
We think you need these skills to ace Freelance QC Analyst – GMP Laboratory Environment in Maidstone
Some tips for your application 🫡
Showcase Your Expertise:In the pharmaceutical industry, it's super important to highlight your specific expertise. Make sure your CV or portfolio reflects your relevant experience—think clinical research, regulatory affairs, or drug development. Don’t forget to include any certifications or training you've completed that are particularly relevant to the role.
Include Case Studies or Project Samples:As a freelancer, your portfolio is your calling card. Include detailed case studies or samples from previous projects that highlight your contributions and results in the pharmaceutical sector. This could be anything from successful clinical trials you've worked on to regulatory submissions—use this to demonstrate your impact.
Articulate Your Availability and Rates:Freelance roles mean flexibility, so clarify your availability upfront. Be transparent about your rates too—this helps set the stage for negotiations. You can mention your preferred working hours and project lengths to align with what Planet Pharma might be looking for.
Tailor Your Cover Letter:Your cover letter should connect the dots between your experience and the needs of Planet Pharma. Use it to explain why you're interested in this freelance role specifically and how your background in the pharmaceutical industry can help solve their unique challenges. Let your personality shine through while remaining focused on professional achievements!
How to prepare for a job interview at Planet Pharma
✨Show Off Your Expertise
Freelancing in the pharmaceutical industry means you'll want to highlight your specialised knowledge. Make sure to showcase your experience with regulatory processes or clinical trials, as these are crucial in this field. Share specific projects you've worked on to demonstrate your capability!
✨Know Your Tools and Tech
If you've worked with any industry-specific software, like LabArchives or Empower, get ready to discuss your experience with them. Being familiar with these tools will set you apart during the interview, as they’re often central to project success in pharmaceuticals. Don’t forget to mention how you’ve used data analysis in your previous roles – it’s key in this sector!
✨Bring Your Portfolio to Life
As a freelancer, your portfolio is your calling card. Prepare a compelling presentation that outlines your previous projects, focusing on results and methodologies. Highlight any case studies or publications to show your contributions to research or development – this can really grab the attention of Planet Pharma.
✨Prepare for Scenario-Based Questions
Expect some scenario-based questions that might challenge your problem-solving skills in real-world contexts. Be ready to discuss how you would handle tight deadlines, regulatory hurdles, or unexpected findings in your projects. This will allow you to demonstrate not just your knowledge, but your practical abilities too!
