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- Tasks: Join us as an Analytical Development Scientist, focusing on method development and quality control.
- Company: Be part of a dynamic team dedicated to innovative analytical solutions in a fast-paced environment.
- Benefits: Enjoy a collaborative culture with opportunities for training and professional growth.
- Why this job: Make a real impact by improving lab efficiency and supporting cutting-edge projects.
- Qualifications: Ideal candidates are detail-oriented, with a background in science and a passion for quality assurance.
- Other info: This role offers a chance to work on diverse projects and enhance your analytical skills.
The predicted salary is between 36000 - 60000 £ per year.
Analytical Development Scientist responsible for analytical method development, validation, technical transfer and routine Quality Control support.
Role
Departmental Operations:
Perform assigned work as agreed with the project lead and/or Analytical Development Manager. Ensure efficient use of time to complete the assigned objectives
Maintain laboratory areas, ensuring procedures are complied with to meet client, regulatory GMP and safety requirements.
Provide training and troubleshooting support to production and stability Quality Control groups.
Provide QC support (if required.)
Engage in specified compliance and improvement projects.
Provide cover for other Analytical Development Scientists as required.
Ensure economic use of labour, materials, energy and services, proposing and implementing measures for cost reduction and waste minimisation to meet the department and site targets.
Identify opportunities for improved methods of working to enhance efficiency, cost control and safety/GMP performance.
Support training of new members of staff to the company / department.
Project Delivery:
Responsible for ensuring that assigned project deliverables are fully completed on time.
Lead aspects of projects as appropriate and in agreement with the Analytical Development Manager.
Plan and carry out work, as agreed with the project lead, to ensure effective project progression in line with customer requirements.
Support method development, technical transfer, qualification and validation activities.
Provide analytical development project support, ensuring compliant introduction into QC, production and stability groups – have involvement in decisions on scheduling of development, technical transfer and validation in conjunction with other technical staff.
Workload planning with other staff to ensure required timelines are met.
Provide QC support if required.
Client communication as required, in a professional manner.
Quality:
Ensure timely close out of deviations, change controls and commitment tracking.
Uphold cGMP principles and ESH standards, continually seek opportunities to improve and enhance standards, and encourage other staff to do likewise.
Record all laboratory work in standard official notebooks and compile results and observations for incorporation into technical reports. Adhere to the relevant procedures.
Follow all appropriate protocols and procedures as required for the work undertaken.
- Ensure accuracy of raw data and analytical interpretations
AD Scientist employer: Piramal Pharma Solutions
Contact Detail:
Piramal Pharma Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land AD Scientist
✨Tip Number 1
Familiarize yourself with the latest analytical methods and technologies relevant to the role. This will not only enhance your knowledge but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the analytical development field. Attend industry conferences or webinars to connect with potential colleagues and learn about current trends and challenges in the industry.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to project delivery and compliance in previous roles. Highlighting your experience in managing timelines and ensuring quality will set you apart.
✨Tip Number 4
Showcase your ability to work collaboratively in a team environment. Be ready to share instances where you've successfully trained others or improved processes, as teamwork is crucial in this role.
We think you need these skills to ace AD Scientist
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the AD Scientist position. Highlight key responsibilities such as analytical method development, validation, and compliance with GMP standards, and reflect your understanding of these in your application.
Tailor Your CV: Customize your CV to emphasize relevant experience in analytical development, project management, and quality control. Include specific examples of past projects where you demonstrated skills in method development and compliance with regulatory requirements.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the job requirements. Discuss your experience with training staff, troubleshooting, and improving laboratory efficiency, and express your enthusiasm for contributing to the company's goals.
Highlight Compliance Knowledge: In your application, make sure to mention your familiarity with cGMP principles and any relevant safety standards. Provide examples of how you've upheld these standards in previous roles, as this is crucial for the position.
How to prepare for a job interview at Piramal Pharma Solutions
✨Understand the Role
Make sure you have a clear understanding of the responsibilities of an Analytical Development Scientist. Familiarize yourself with analytical method development, validation, and quality control processes, as these will likely be key discussion points during your interview.
✨Showcase Your Experience
Prepare to discuss specific examples from your past work that demonstrate your ability to manage projects, ensure compliance with GMP standards, and provide training or troubleshooting support. Highlight any relevant achievements that showcase your skills in analytical development.
✨Emphasize Team Collaboration
This role requires working closely with various teams. Be ready to talk about your experience in collaborating with project leads, production groups, and other scientists. Discuss how you’ve contributed to team success and improved efficiency in previous roles.
✨Prepare for Technical Questions
Expect technical questions related to analytical methods, quality control, and regulatory compliance. Brush up on your knowledge of cGMP principles and be prepared to discuss how you would handle specific scenarios related to method development and validation.
