At a Glance
- Tasks: Ensure product quality and compliance in a fast-paced pharmaceutical environment.
- Company: Join a leading pharmaceutical manufacturing organisation focused on quality and patient safety.
- Benefits: Gain valuable experience, work collaboratively, and develop your career in a dynamic field.
- Other info: Collaborative culture with opportunities for growth and exposure to diverse projects.
- Why this job: Be at the forefront of quality assurance and make a real impact on patient safety.
- Qualifications: Degree in a scientific discipline and previous QA experience in regulated environments.
The predicted salary is between 29700 - 36300 £ per year.
Are you an experienced Quality Assurance professional looking to develop your career within a fast-paced pharmaceutical environment? We are recruiting for a QA Officer to join an established pharmaceutical manufacturing organisation. This is an excellent opportunity to take ownership of quality activities across new products, manufacturing campaigns and change projects, while helping to maintain high standards of product quality, regulatory compliance and patient safety.
The Role
As QA Officer, you will act as the Quality Assurance representative for key projects and manufacturing activities. You will review critical documentation, support investigations and audits, and work closely with cross-functional teams to identify and resolve potential GMP/GxP compliance issues.
Key Responsibilities
- Review and approve manufacturing batch records, packaging records, laboratory data and process instructions.
- Act as the QA representative for new products, manufacturing campaigns and change projects.
- Manage and support deviations, non-conformances, investigations and out-of-specification results.
- Contribute to root cause analysis and the implementation of corrective and preventive actions.
- Participate in change controls, risk assessments, validation activities and product quality reviews.
- Support internal audits, customer audits and regulatory inspection readiness.
- Maintain Quality Management System documentation, including SOPs, protocols, reports and quality records.
- Support material and product disposition activities.
- Work collaboratively with Production, QC, R&D and other departments to resolve quality-related issues.
- Prepare quality trend reports and clearly communicate findings to relevant stakeholders.
- Promote a strong culture of quality, compliance and continuous improvement.
About You
- Degree qualified in Pharmacy, Chemistry, Biology or another relevant scientific discipline.
- Previous Quality Assurance experience within the pharmaceutical industry or another closely regulated environment.
- Strong working knowledge of GMP/GxP requirements.
- Knowledge of MHRA and FDA regulatory requirements would be advantageous.
- Experience working with Quality Management Systems and controlled documentation.
- Practical experience supporting batch record review, deviations, investigations, CAPA and change controls.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and organisational ability.
- Confident written and verbal communicator who can explain complex quality matters clearly.
- Able to work independently while contributing effectively within a cross-functional team.
Why Apply?
This is a varied opportunity offering exposure to projects, audits, investigations, validation and product lifecycle activities. You will join a collaborative pharmaceutical environment where quality, compliance and patient safety are at the heart of operations. Apply today to take the next step in your pharmaceutical Quality Assurance career.
QA Officer in Falkirk employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land QA Officer in Falkirk
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like SRG. 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 SRG.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like SRG. 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 SRG is looking for. A tailored application can really make you stand out!
We think you need these skills to ace QA Officer in Falkirk
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 SRG!
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 SRG 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 SRG!
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 SRG, 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 SRG
✨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 SRG 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 SRG’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.
