At a Glance
- Tasks: Lead and develop analytical methods for drug development in a dynamic environment.
- Company: Piramal Pharma Solutions, a global leader in pharmaceutical solutions.
- Benefits: Ongoing training, career advancement, and a supportive culture.
- Other info: Collaborate with passionate professionals and enjoy a culture of innovation.
- Why this job: Make a real-world impact in the life sciences industry with innovative projects.
- Qualifications: Degree in Analytical Chemistry or related field; experience in GMP environments.
The predicted salary is between 36000 - 60000 € per year.
At Piramal Pharma Solutions, we are driven by a purpose: to help patients around the world live healthier, longer lives. As part of our continued growth, we’re seeking an Analytical Development Scientist to support and lead method development, validation, and technical transfer activities in a dynamic, GMP-compliant environment.
Your Role
You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance.
Key Responsibilities
- Develop, validate, and transfer robust analytical methods for raw materials, intermediates, and finished products.
- Drive timely and compliant execution of project deliverables, ensuring alignment with client expectations.
- Collaborate cross-functionally to plan, schedule, and manage project work across QC, production, and stability teams.
- Participate in client communications and technical discussions, providing expert input and updates as needed.
- Conduct method development and troubleshooting using state-of-the-art instrumentation (e.g., HPLC, GC, UV, etc.).
- Author and review technical documentation including protocols, reports, and SOPs in accordance with cGMP standards.
- Provide analytical expertise during technology transfer to QC and production environments.
- Support analytical training and mentoring for junior staff and cross-functional teams.
- Maintain meticulous laboratory records and ensure all work complies with GMP, safety, and data integrity standards.
- Actively contribute to investigations, deviation reports, and change controls.
- Identify opportunities for process optimization, cost reduction, and waste minimisation.
What We’re Looking For
- A degree (BSc/MSc/PhD) in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline.
- Solid experience in analytical method development and validation in a GMP-regulated environment.
- Strong understanding of ICH guidelines and regulatory requirements.
- Hands-on experience with a range of analytical techniques and instrumentation.
- Excellent problem-solving, communication, and project management skills.
Why
- Be part of a global CDMO with a strong reputation in delivering high-quality, end-to-end pharmaceutical solutions.
- Collaborate with passionate scientists and professionals in a supportive, innovation-focused culture.
- Access ongoing training, development, and career advancement opportunities.
- Make a real-world impact in the life sciences industry.
Locations
AD Scientist in Falkirk, Grangemouth employer: Piramal Pharma Solutions
At Piramal Pharma Solutions, we pride ourselves on being an exceptional employer, offering a collaborative and innovation-driven work culture that empowers our employees to make a meaningful impact in the life sciences industry. With access to ongoing training and career advancement opportunities, our Analytical Development Scientists play a crucial role in supporting new drug development while working in a dynamic, GMP-compliant environment. Join us to be part of a global leader dedicated to improving patient health and well-being.
StudySmarter Expert Advice🤫
We think this is how you could land AD Scientist in Falkirk, Grangemouth
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and showcasing your analytical skills. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience effectively.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. At StudySmarter, we encourage you to check out our website for tailored job opportunities that match your expertise in analytical development.
✨Tip Number 4
Follow up after interviews! A simple thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which are key traits in the pharmaceutical field.
We think you need these skills to ace AD Scientist in Falkirk, Grangemouth
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Analytical Development Scientist role. Highlight your experience in method development and validation, and don’t forget to mention any hands-on experience with analytical techniques like HPLC or GC.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about helping patients live healthier lives and how your skills align with our mission at Piramal Pharma Solutions.
Showcase Your Problem-Solving Skills:In your application, give examples of how you've tackled challenges in a GMP-compliant environment. We love to see candidates who can think on their feet and come up with innovative solutions!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Piramal Pharma Solutions
✨Know Your Analytical Techniques
Make sure you brush up on the analytical techniques mentioned in the job description, like HPLC and GC. Be ready to discuss your hands-on experience with these methods and how you've applied them in a GMP-compliant environment.
✨Showcase Your Project Management Skills
Prepare examples of how you've led projects or collaborated cross-functionally in previous roles. Highlight your ability to manage timelines and deliverables while ensuring compliance with client expectations.
✨Understand Regulatory Standards
Familiarise yourself with ICH guidelines and other regulatory requirements relevant to the role. Being able to discuss these standards confidently will show that you’re serious about compliance and quality in your work.
✨Prepare for Technical Discussions
Anticipate questions related to method development and troubleshooting. Think of specific challenges you've faced and how you resolved them, as well as any contributions you've made to technical documentation or training.
