AD Scientist

ZipRecruiter; Grangemouth; On-site; GBP 35,000 - 45,000; Full time

Job summary

A leading pharmaceutical company in Grangemouth is seeking an experienced Analytical Development Scientist to support method development, validation, and technical transfer activities in a GMP-compliant environment. Candidates should hold a degree in Analytical Chemistry or a related field and possess solid experience in analytical method development. This role involves collaboration across teams and project management responsibilities.

Benefits

Ongoing training and development

Career advancement opportunities

Impact in the life sciences industry

Qualifications

• Solid experience in analytical method development and validation.
• Strong understanding of ICH guidelines and regulatory requirements.
• Hands-on experience with a range of analytical techniques.

Responsibilities

• Develop, validate, and transfer robust analytical methods.
• Drive timely execution of project deliverables.
• Maintain compliance with GMP and data integrity standards.

Skills

Analytical method development

Project management

Problem-solving

Communication

GMP compliance

Education

Degree in Analytical Chemistry or related discipline

Tools

HPLC

GC

UV spectroscopy

Job description

Job Description

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

Project Leadership & Delivery

• 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.

Technical & Operational Excellence

• 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.

Compliance & Continuous Improvement

• 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