Manufacturing Engineer to SOBI

On behalf of our client Sobi, QRIOS Life Science is now looking for a Manufacturing Engineer for a consultant assignment. Are you an analytical person who has a problem solving mindset and an ability to work independently and to make priorities in order to deliver business critical items in time. Don´t hesitate to apply for this position. Selections and interview are held on an ongoing basis, please submit your application as soon as possible.

About the position
Are you looking for a new dynamic role where you get to collaborate and build a network with people from different backgrounds and nationalities while you support deliver rare medicines to patients around the world? At Sobi we have a great opportunity within our External Drug Substance and Drug Product manufacturing group, we are looking for a driven External Manufacturing Engineer on a temporary basis to be part of our team and work within different cross-functional groups to ensure that activities, projects and tasks are coordinated and executed to ensure supply, all of this while we hold ourselves to GMP requirements and deliver our products with the right quality. If this sounds interesting please keep reading the job description and apply on the button below!

Responsibilities
• Participate in cross functional Virtual Plant Team (DS, DP, CLO as applicable)
• Operational CMO/CLO management tasks including coordination
• Participate in meetings with CMO/CLO as applicable
• Support Supplier relationship management for CMO(s), for example POs, improvements and support for OTIF delivery
• When applicable, DS and DP allocations and calculations.
• Lead or participate in internal activities related to external manufacturing such as change management, deviations and CAPAs
• Issue and or review applicable external and internal SOP’s and manufacturing instructions
• Budget input and adherence for CMO/CLO related costs
• Lead or participate in projects
• Driving continuous improvements in order to maintain efficient ways of working internally and at external network

Your profile
• University degree in Biotechnology or other relevant scientific fields, or equivalent work experience
• 5 years of experience in the pharmaceutical industry coupled to drug substance (both up and downstream processing) and/or drug product manufacturing
• Min 2 years’ experience from coordinating roles, including Project Management
• Good knowledge of cGMP manufacturing of biologics and/or small molecule pharmaceuticals, including investigating deviations and change management
• Previous work experience involving direct contact with CMO´s/CLO’s or other external parties
• Good knowledge of MS Office and hands on experience of digital systems
• Ability to work in a cross functional matrixed environment and to successfully collaborate with internal and external parties

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.


Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered.