At a Glance
- Tasks: Inspect and label drug products, ensuring quality control for commercial batch release.
- Company: Join a leading pharmaceutical company with a focus on innovation.
- Benefits: Competitive pay at £13.58 per hour, with potential for contract extension or permanent role.
- Other info: Opportunity for career growth and referral incentives available.
- Why this job: Make a real impact in the pharmaceutical industry while developing your skills.
- Qualifications: Degree in a scientific subject and hands-on experience in cGXP lab environments.
The predicted salary is between 13.58 - 13.58 £ per hour.
Quality Control Analyst GMP / GLP – Swindon
Opportunity
Are you currently working in quality control and or quality assurance?
Does your experience include the testing, inspection and labelling of drugs for product release?
Do you have hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products?
Want to work for a large pharmaceutical company?
Yes then this is the role for you!
Your role as a Quality Control Analyst GMP / GLP based in Swindon will involve inspecting and labelling commercial finished drug product batches.
The position is necessary to maintain testing to support for commercial batch release.
Duties and responsibilities include
- Driving the 5S methodology within QC.
- Managing QC metrics and compliance activities including deviations, CAPAs, and change controls.
- Writing and reviewing SOPs and technical reports (COAs, cleaning certificates, validation protocols, etc.)
- Ensuring adherence to data integrity and regulatory requirements across all lab systems.
- Staying current with industry innovations in particle size technology.
This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance.
The PAYE rate is £13.58 per hour.
Skills
To apply for the Quality Control Analyst GMP / GLP role you will have the following skills:
- Degree or equivalent in a scientific subject.
- Hands-on experience in c GXP lab environments.
- Need to be clean-shaven due to working in clean rooms.
- No make up, false eye lashes and nail varnish due to working in clean rooms.
- Experience with HPLC Empower, method development, troubleshooting, and validation.
- Familiar with particle size technologies (preferred).
How to Apply
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat.
Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please don’t hesitate to contact us.
If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300.
We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Control Analyst GMP / GLP in Devizes employer: Quality Start Careers
Join a dynamic and innovative medical device development company in Walsall, where your expertise as a Test Quality Assurance Engineer will be valued and nurtured. With a strong focus on employee growth, we offer comprehensive training and development opportunities, alongside a collaborative work culture that encourages creativity and teamwork. Enjoy the unique advantage of working in a sector that directly impacts healthcare, while being part of a supportive team dedicated to delivering high-quality products.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Analyst GMP / GLP in Devizes
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Quality Start Careers. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Quality Start Careers.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Quality Start Careers. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Quality Start Careers is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Quality Control Analyst GMP / GLP in Devizes
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Quality Start Careers!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Quality Start Careers that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Quality Start Careers!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Quality Start Careers, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Quality Start Careers
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Quality Start Careers that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Quality Start Careers’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
