EPDM Scientist – Gothenburg

Are you a scientist with GMP-manufacturing experience from the pharmaceutical industry? Then this role might be the one for you!

Our customer in gothenburg is looking for a Scientist with excellent collaboration, communication, and planning skills with a strong sense of responsibility, team work and delivery focus. Within the EPDM manufacturing unit, in the GMP (Good Manufacturing Practice) arena, you will make an important contribution in delivering clinical results in the development of new medicines. This role revolves around the manufacturing of drug product where all activities will have a significant impact on the speed, quality and cost of the customer development portfolio.

Purpose, Offer and Benefits

In joining EPDM and PharmSci, you will be part of an amazing group of skilled and driven colleagues who truly embrace team spirit, who you will exchange knowledge and collaborate with on many levels in various contexts. This provides excellent opportunities for your professional development, and possibilities to take on further accountabilities in line with your personal growth

Your Responsibilities

We expect the successful candidate to:

• Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
• Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform transactions in material management systems.
• Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
• Rapidly develop strong competence within relevant process technologies and build credibility and ability to drive and secure product establishment, scale-up and clinical manufactures.
• Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
• Assess records and report manufacturing and validation data accurately according to GMP.
• Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure the companys Policies and Standards are understood and followed.
• Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for the companys customers and patients.

The Bigger Picture

The company is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services.

This is a 6 months consulting assignment with a chance of extension.

The advantages of being a consultant are many! Not only do you get to work with interesting companies and try many different tasks. You also get to broaden your network that you can benefit from throughout your future career

Our Expectations

Do you have the essential qualifications for this role?

Strong verbal and documentation skills in English is a requirement. We expect you to have a keen interest to learn and operate complex manufacturing equipment and develop your expertise in pharmaceutical process technology. Experience from pharmaceutical development or working in a manufacturing or supply chain organisation and knowledge of cGMP is a merit for this role.

To be considered for this role, you need to have a MSc in pharmacy/engineering and/or extensive GMP-manufacturing experience from the pharmaceutical industry.