Vacant job

Job Description

Are you an experienced analytical chemist with expertise in UPLC and method validation? Do you want to take on a leading role in exciting projects within Life Science? We are currently looking for a Senior Validation Lead for a consultancy assignment with one of our distinguished clients.

In the role of Senior Validation Lead, you will have overall responsibility for driving, planning, and executing projects related to the development and validation of analytical methods, with a special focus on UPLC. You will act as the link between the laboratory, Quality Assurance (QA), and regulatory requirements. This is a key role for you if you thrive with significant autonomy, complex problem-solving, and a desire to contribute your expertise in a strictly regulated environment (GMP).

Working as a consultant at Randstad Life Science means getting the best of both worlds: the security of a stable employment with collective agreements, benefits, and a dedicated consultant manager, combined with the flexibility and development opportunities of working on various exciting assignments. We support your career and match your skills with assignments where you can truly make a difference and continue to grow as an expert.

Responsibilities

• Lead and plan validation projects for analytical methods from start to finish.
• Develop, optimize, and validate analytical methods with a focus on UPLC and associated detectors.
• Create and review validation documentation such as plans, protocols, and final reports in accordance with current regulatory requirements (e.g., ICH guidelines and GMP).
• Act as a technical expert and provide advice during method transfers and troubleshooting of chromatographic deviations.
• Collaborate closely with cross-functional teams, including QA, production, and external partners, to ensure the highest quality and regulatory compliance.

Qualifications

• Education: University degree in natural sciences or engineering (e.g., chemistry, biotechnology, pharmacy) or equivalent experience.
• Experience: Several years (senior level) of experience in analytical method development and validation within the pharmaceutical or biotechnology industry.
• Technical Expertise: In-depth practical and theoretical knowledge of chromatography, specifically UPLC.
• Regulatory Knowledge: Strong experience working in a GMP-regulated environment and a good understanding of international guidelines (e.g., ICH Q2).
• Languages: Fluent in both Swedish and English, both verbally and in writing (as documentation is conducted at a strict regulatory level).
• Personal Attributes: You are structured, meticulous, and have strong communication skills that enable you to naturally lead and engage others in the project.

About the Company

Randstad

At Randstad, we know that every person has a place in the labor market. With operations throughout the country and across all competency areas, we help people find a job that feels right, where they have the opportunity to grow, develop, and achieve their full potential.

With nearly 600,000 employees in 38 countries, Randstad is the world leader in HR services, with the goal of becoming the world's premier and most appreciated partner in the labor market. By combining our passion for people with the power of today's technology, we help people and companies achieve their full potential. We call it Human Forward.