At a Glance
- Tasks: Conduct analytical testing for pharmaceutical products and ensure compliance with quality standards.
- Company: Join a leading International Medical Solutions business in Farnham.
- Benefits: Competitive salary, completion bonus, pension, healthcare, and professional development.
- Other info: Dynamic team environment with opportunities for career growth and improvement programs.
- Why this job: Make a real impact in the pharmaceutical industry while gaining valuable experience.
- Qualifications: Science education and relevant experience in an analytical laboratory preferred.
The predicted salary is between 35000 - 45000 £ per year.
My Client, an International Medical Solutions business, is hiring a QC Analyst for their Farnham based team. The salary range is £28k-£36k (pro rata) depending on experience. This is a 6-month FTC as an employee with a 5% completion bonus, and includes access to pension and healthcare.
The role provides analytical testing support for all pharmaceutical products manufactured at the Farnham site. Following the clients Quality Standards or Pharmacopoeia methods, testing will cover:
- Raw materials
- Excipients
- Components
- In-process samples
- Finished products
Testing will include a high proportion of visual and physical measurements associated with the testing of components. Responsibilities will also include:
- Performing qualitative tests or quantitative assays on samples using techniques that vary from standard analytical equipment to highly modern and automated instrumentation.
- Documenting all work in a compliant manner.
- Participating in OOS investigations.
- Reviewing analytical results to ensure accuracy and compliance to test methods.
- Preparation of all laboratory documentation.
- Ensuring that departmental objectives are implemented in line with the overall Quality/Corporate goals.
- Complying with all safety and GMP requirements within the Laboratory.
- Planning a daily schedule to meet testing requirements.
- Preparing and timely submission of test samples from raw materials, in-process and final product samples to both internal laboratories and external test houses.
- Operating laboratory equipment including daily upkeep and maintenance and assisting in troubleshooting when required.
- Working to Standard Operating Procedures/WIs, completing the sampling, inspection and analysis of Raw Materials or Components, In-Process and Final Product samples to defined Chemical, Physical and Pharmacopoeia test procedures to support Manufacturing and Development activities.
- Documenting all testing activities to regulatory standards.
- Reviewing analytical results to ensure accuracy and compliance to both test methods and registered specifications.
- Preparation and revision of laboratory protocols, reports, procedures and WIs.
- Assisting in the Innovation and development of analytical processes to meet internal and international method validation requirements to support any QC, R&D or Manufacturing activity.
- Leading OOS/OOT investigations, utilising technical knowledge to identify assignable cause and corrective actions.
- Leading and participating in investigations for Quality Events, Complaints and review/generation of Change controls.
- Managing information to support monitoring and evaluation of cGMP compliance including Key Performance Indicators (KPI).
- Preparing metrics to visualise KPIs.
- Participating in and facilitating improvement programs within the Laboratory.
- Participating in multi-functional teams to support project assignments.
- Ensuring that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with the Clients values.
- Completing additional tasks considered necessary to meet business and customer requirements as indicated by the team leader.
- Carrying out other reasonable tasks as required by the Team leader.
Education and Experience
- Be educated in science or related discipline.
- Possess relevant experience in the Pharmaceutical Industry.
- 1-2 years experience in an analytical Laboratory is preferable.
- A knowledge of quality systems and the experience of working in a regulated environment preferred.
- Have a good knowledge of GLP/GMP.
- Knowledge and experience in the following analytical techniques: Gas chromatography and HPLC/UPLC.
- An understanding and application of COSHH regulations in a chemical industry.
- Demonstrated advanced computer skills, Microsoft Office preferred.
- Good written and verbal skills.
- To perform precise and constant analysis in support of analytical testing.
- To complete assignments in a timely manner and communicate progress at intervals.
- To analytically evaluate results.
- Be a self-starter capable of delivering consistent results to a high level.
- Must be a team player and be able to interact with colleagues in a constructive and positive manner.
QC Analyst 6 month contract in Guildford employer: DRH Support Services
Join an esteemed International Medical Solutions business in Farnham as a QC Analyst, where you will be part of a dynamic team dedicated to ensuring the highest quality standards in pharmaceutical products. With a supportive work culture that prioritises employee well-being, you will benefit from competitive compensation, a completion bonus, and access to healthcare and pension plans. This role offers excellent opportunities for professional growth and development within a regulated environment, making it an ideal place for those seeking meaningful and rewarding employment.
StudySmarter Expert Advice🤫
We think this is how you could land QC Analyst 6 month contract in Guildford
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like DRH Support Services.
We think you need these skills to ace QC Analyst 6 month contract in Guildford
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at DRH Support Services.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at DRH Support Services. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at DRH Support Services
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with DRH Support Services.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help DRH Support Services achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
