Vacant job

Job Description

At Randstad Life Sciences, we are looking for someone who wants to work on an exciting assignment with one of our clients in Strängnäs. We see an increased demand for technical expertise, and if you are interested in working with process support, deviation management, and continuous improvements in a production environment, you have come to the right place!

As a consultant at Randstad Life Sciences, we are your employer, but your daily workplace will be with one of our clients. Your consultant manager is always close at hand, both during and between assignments, to help you develop your career in the direction you dream of. As a consultant with us, you will receive a competitive salary, benefits, and collective agreement terms. We are attentive to your wishes regarding assignments and tasks, and with our broad client portfolio in Mälardalen, we will together adapt your continued career based on your skills, experience, and ambitions. At Randstad Life Sciences, we have a holistic approach to what a consulting assignment entails, which means you have opportunities with us. You will be part of a larger consulting team within Life Sciences, giving you the chance to broaden your network and gain valuable experience from various workplaces.

You will belong to the TIM – Technology Investigation Management group. This is the role for you who want to specialize in the investigation craft itself. Your team is responsible for deviation investigations that span the entire flow: from raw materials and production to the quality organization.

As a process engineer, you act as the project manager for your deviations. You lead cross-functional groups to identify root causes using Six Sigma tools and implement robust corrective actions (CAPA) that prevent the errors from occurring again.

As a consultant at Randstad Life Sciences, you will receive a secure employment with collective agreements and benefits, while also having the opportunity to develop with one of the industry's most attractive employers.

The assignment starts immediately and runs until after the summer. For the right person, there are excellent opportunities for extension or direct recruitment to the client.

Access to 50% remote work after training!

Start date: Immediate

Responsibilities

• Lead and document deviation investigations within quality, production, and raw materials.
• Drive troubleshooting and ensure that work meets set timelines.
• Contribute to developing the site's quality culture and ensuring cGMP compliance.
• Participate in inspections and work on continuous improvements.

Qualifications

• University degree in a scientific subject.
• Good knowledge of and understanding of cGMP.
• Fluent in Swedish and English, both spoken and written.
• Good communication skills.
• Experience from the pharmaceutical industry.

Meritorious:

• Previous experience leading deviation investigations.
• Knowledge of Lean and Six Sigma.
• Ability to handle uncertainties and drive processes forward independently.

About the Company

Randstad

At Randstad, we know that everyone has a place in the labor market. With operations across the country and in all areas of expertise, we help people find a job that feels good, where they can grow, develop, and reach their full potential.

With nearly 600,000 employees in 38 countries, Randstad is a world leader in HR services, aiming to become the world's leading 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.