At a Glance
- Tasks: Lead technical projects in the QC lab and manage a team of specialists.
- Company: Join Eisai, a leading pharmaceutical company focused on human healthcare.
- Benefits: Competitive salary, bonus, free parking, and learning opportunities.
- Other info: Dynamic role with excellent career growth and a focus on well-being.
- Why this job: Make a real impact in healthcare while working with cutting-edge technology.
- Qualifications: Degree in science and experience with QC equipment and electronic systems.
The predicted salary is between 45000 - 55000 £ per year.
Eisai is a leading research-based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. Eisai Manufacturing is the hub of Eisai’s production and supply chain. We make tablets, package these into blisters, label and package vials and bottles. We also manage the wider medicines supply chain and other companies who undertake work on our behalf. By joining Eisai, you will be working for an organisation with a human healthcare philosophy, which means that we put the patient first in everything we do.
This job is responsible for the management of all technical projects within the QC laboratory. This includes leading a team of technical specialists that will manage laboratory electronic systems (e.g. LIMS and CDS), the introduction and maintenance of new or existing equipment and technologies, and leading laboratory compliance-related activities (e.g. global change, new product introduction, method transfer and pharmacopeia reviews).
The role is responsible for:
- Ensuring effective management of a team of technical specialists.
- Ensuring QC Equipment and Electronic Systems are managed effectively to ensure their use in the manufacture, packaging and testing of marketed drug products comply with department Standard Operating Procedures, current GMP, Data Integrity guidelines and Eisai Corporate expectations.
- Creating and maintaining a five-year equipment replacement plan to ensure the QC laboratory is equipped with current equipment and software that meet the testing requirements.
- Ensuring effective management of New Product Introduction and Method Transfer.
- Ensuring effective management of QC compliance activities (e.g. global changes and pharmacopeia compliance).
- Ensuring effective management of the education and training of QC team members in the use of specialist equipment and software.
- Reviewing and approving of any associated SOPs and quality policies, as required.
- Leading change management processes to ensure equipment and system data are continuously available and functioning as intended.
What are we looking for?
- Degree or equivalent experience in a science discipline.
- Strong working knowledge of pharmaceutical Quality Control Equipment and Electronic systems, including their qualification and validation.
- Significant previous experience (at least two years) in the technical management of QC Equipment and Electronic Systems.
- Experienced as a laboratory administrator and/or end user of QC electronic systems.
- Excellent communication and good people management skills to support progression of technically led projects internally and externally.
- Ability to establish and maintain effective working relationships and communication links within EML, affiliated organisations and other customers.
- Ability to understand and analyse user requirements to facilitate changes and system improvements.
- Good understanding of the requirements of data integrity and application to system management.
- Good technical and scientific judgement.
- Ability to interpret complex data and present key findings.
- Ability to describe technical information in easy-to-understand terms.
- Computer literate e.g. Word, Excel and PowerPoint.
- Thorough understanding of GMP Guidelines and Regulations.
- Maintain knowledge and understanding of technical advancements in QC Equipment and Electronic systems.
What we offer in return
Eisai offers a competitive salary and excellent wider benefits package that includes:
- Electric charging points for Electric/Hybrid vehicles.
- Discretionary Bonus.
- Free onsite parking.
- Subsidised onsite restaurant and coffee shop.
- Learning and development opportunities.
- Retail discounts.
- Well-being.
Quality Control Technical Project Manager - Permanent Position employer: Eisai EMEA
Eisai is an exceptional employer that prioritises a human healthcare philosophy, ensuring that employees contribute to meaningful work that puts patients first. With a competitive salary and a comprehensive benefits package, including hybrid working options and extensive learning opportunities, Eisai fosters a collaborative and inclusive culture at its EMEA Knowledge Centre. Employees can thrive in an environment that values diversity, well-being, and personal growth, making it a rewarding place to advance your career as a Financial Analyst.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Technical Project Manager - Permanent Position
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Eisai EMEA. 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 Eisai EMEA.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Eisai EMEA. 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 Eisai EMEA is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Quality Control Technical Project Manager - Permanent Position
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 Eisai EMEA!
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 Eisai EMEA 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 Eisai EMEA!
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 Eisai EMEA, 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 Eisai EMEA
✨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 Eisai EMEA 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 Eisai EMEA’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.