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- Tasks: Supervise and execute quality control tests for pharmaceutical products.
- Company: Piramal Pharma Solutions, a leader in pharmaceutical services.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Join a dynamic team and ensure the highest quality standards in healthcare.
- Qualifications: Experience in quality control and knowledge of cGMP practices.
- Other info: Collaborative environment with a focus on continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
BUSINESS: Piramal Pharma Solutions
DEPARTMENT: Quality Control
LOCATION: Grangemouth
Job Overview
To supervise and execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and protocols and in accordance with best cGMP work practices, Quality standards and metrics.
Reporting Structure
Reports to QC Team Leader (Clinical ADC)
Key Roles/Responsibilities
- Execute analytical procedures for testing of raw materials, in process products, bulk drug substance, final products and stability products according to defined SOPs and protocols and ensure that the QC team is in compliance with the same.
- Apply best cGMP work practices and techniques to test and release raw materials, in process products, bulk drug substance, final products and stability products within specification.
- Ensure that all QC analysts are appropriately trained and competent in the procedures they are conducting, and are in compliance with best cGMP working practices at all times.
- Conduct on-time reporting according to the defined and trained document management standards including review and verification of analytical data provided by the QC Analysts.
- Immediately escape and report any deviations to materials, facilities, processes or procedures to the QC Manager.
- Be accountable for the analytical laboratories being clean, tidy and well organized and in a state of continuous inspection readiness.
- Conduct all activities in the most careful and safe manner and in full compliance with ESH requirements.
- Ensure that at any time equipment, facilities and materials used in the area of responsibility comply with defined standards.
- Issue, manage and close-out deviations, change controls, OOS or SST investigations and CAPAs in a timely fashion.
- Identify areas for continuous improvement and elevate those to the QC Manager.
- Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting.
- Support installation, qualification and periodic review of equipment.
- Support the transfer of new methods and techniques into Quality Control.
- To undertake any other duties as requested by the line manager in accordance with company requirements.
Senior QC Analyst in Falkirk employer: Piramal
Contact Detail:
Piramal Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QC Analyst in Falkirk
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma industry, especially those who work in quality control. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on cGMP practices and analytical procedures. We want you to be ready to showcase your knowledge and experience, so practice answering common QC-related questions with confidence.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in the interviewer's mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit.
✨Tip Number 4
Apply through our website for the best chance at landing that Senior QC Analyst role. We love seeing applications directly from candidates who are keen on joining our team, so don’t hesitate to hit that apply button!
We think you need these skills to ace Senior QC Analyst in Falkirk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior QC Analyst role. Highlight your experience with cGMP practices and any relevant analytical procedures you've executed. We want to see how your skills match what we're looking for!
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 you can contribute to our team. Be sure to mention specific experiences that relate to the job description.
Showcase Your Team Spirit: We value collaboration, so don’t forget to mention any experiences where you’ve worked well in a team. Share examples of how you’ve contributed to a supportive environment or helped train others in compliance with best practices.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and keep track of it. Plus, you’ll get to see more about our company culture!
How to prepare for a job interview at Piramal
✨Know Your cGMP Basics
Make sure you brush up on your cGMP knowledge before the interview. Understanding current Good Manufacturing Practices is crucial for a Senior QC Analyst role, so be ready to discuss how you've applied these principles in your previous positions.
✨Showcase Your Analytical Skills
Prepare to talk about specific analytical procedures you've executed in the past. Highlight your experience with testing raw materials and final products, and be ready to explain how you ensure compliance with SOPs and protocols.
✨Emphasise Team Collaboration
This role requires a supportive and collaborative environment, so think of examples where you've contributed to team success. Discuss how you've trained others or improved team processes, as this will show you're a great fit for their culture.
✨Be Ready for Problem-Solving Questions
Expect questions about how you've handled deviations or OOS results in the past. Prepare specific examples that demonstrate your ability to manage issues effectively and your commitment to continuous improvement.
