At a Glance
- Tasks: Lead the QC Equipment Team and manage quality control processes for various products.
- Company: Piramal Pharma Solutions, a global leader in drug development and manufacturing.
- Benefits: Competitive salary, training opportunities, and a collaborative work environment.
- Other info: Join a supportive team focused on continuous improvement and innovation.
- Why this job: Be a key player in ensuring product quality and compliance in a dynamic industry.
- Qualifications: Experience in quality control and strong leadership skills required.
The predicted salary is between 37800 - 46200 £ per year.
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider and experience with various technologies enables us to serve Innovator and Generic companies worldwide.
Team Lead for the QC Equipment Team. To manage and co-ordinate Quality Control department equipment required for the release testing of raw materials, in process products, bulk drug substance, final products. To be the point of contact for client projects, manage expectations and requirements and deliver against the S&OP.
- Be the Subject Matter Expert (SME) for all Analytical Equipment aligned to client projects.
- Be the Subject Matter Expert (SME) for all QC activities aligned to client projects.
- Manage 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 manage the testing and release of raw materials, in process products, bulk drug substance, final products and stability products within specification and in accordance with Data Integrity requirements, Annex 11 Computerised Systems and 21CFR part 11 Good Documentation Practices for Electronic Data.
- Ensure that all QC Analysts and QC Technicians are appropriately trained and competent in the procedures they are conducting, and are in compliance with best cGMP working practices at all times.
- Ensure subcontract of QC testing and dispatching to approved suppliers is performed according to defined procedures and in compliance with GMP.
- Manage on-time reporting according to the defined and trained document management standards including review and verification of analytical data provided by the Senior QC Analysts and QC Analysts.
- Immediately escalate 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 escalate those to the QC Manager.
- Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team-setting.
To undertake any other duties as requested by the line manager in accordance with company requirements.
QC Team Leader (Technical Support) in Grangemouth employer: Piramal Pharma
Piramal Pharma Solutions is an exceptional employer, offering a dynamic work environment in Grangemouth where innovation and teamwork thrive. With a strong commitment to employee development, we provide ample opportunities for growth and skill enhancement, ensuring that our Maintenance Engineers are equipped to tackle exciting challenges while contributing to the success of our engineering systems. Our culture prioritises safety, collaboration, and excellence, making it a rewarding place to build a meaningful career.
StudySmarter Expert Advice🤫
We think this is how you could land QC Team Leader (Technical Support) in Grangemouth
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Piramal Pharma. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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We think you need these skills to ace QC Team Leader (Technical Support) in Grangemouth
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 Piramal Pharma!
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 Piramal Pharma 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 Piramal Pharma!
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 Piramal Pharma, 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 Piramal Pharma
✨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 Piramal Pharma 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 Piramal Pharma’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.
