NorthX Biologics AB jobb

NorthX Biologics is a Contract Development and Manufacturing Organization [CDMO] that offer services and support in the development and manufacturing of biologics used in vaccines, gene therapy and other advanced applications. We have a long tradition of pharmaceutical manufacturing and have been manufacturing GMP biologics since 1992. In 2021 we were recognised as a national innovation hub for advanced therapeutics and vaccines and have expanded our development capabilities to serve our clients. This includes a new development organisation with cutting edge laboratories and technologies. We are looking for a Laboratory Engineer to join our Analytics team, at our Stockholm site, with starting date at the earliest convenience. You will be preforming quality control analysis using broad range of methods, including molecular biology assays, cell-based assays, micro biological assays and HPLC. You will be planning, executing, and reporting experiments to develop robust and reproducible methods that can be validated for GMP. You will be working extensively hands-on in the laboratory, but also responsible for maintenance of qualified status of room and laboratories and instruments, as wells as documenting and writing. For this position we require a minimum a BSc in Biology, Chemistry, or relevant field, and at least 1+ years of GMP experience from the pharmaceutical industry. You must be able to demonstrate strong written and verbal communication skills and be fluent in English and Swedish. Technical skills required for the position. Molecular biology methods such as ELISA, qPCR, Westen blot, SDS · Cell Culture using aseptic techniques HPLC protein analysis Basic microbiology Examples of daily work tasks: Planning, executing, analysing and reporting of routine QC analysis Develop and troubleshoot protocols and methods · Work accordance with appropriate Safety, Health & Environment standards · Work accordance with quality and compliance standards i.e. GMP Participate in method transfer for GMP validation Laboratory maintenance Ordering materials and reagents Upkeep of inventory lists Writing, implementing, and updating documentation Performing deviation investigations Maintaining the qualified status of instruments. As a person, you are responsible, meticulous and find it easy to cooperate with others as well as to work independently. You enjoy working in a structured laboratory environment according to established routines. You love to solve problems by thinking outside the box and you have an eye for details. You have a calm, rigorous and focused approach to experimental. Finally, you are a positive person who is flexible in terms of your daily tasks.

NorthX Biologics is a Contract Development and Manufacturing Organization that offer services and support in the development and manufacturing of biologics used in vaccines, gene therapy and other advanced applications. We have a long tradition of pharmaceutical manufacturing and have been manufacturing GMP biologics since 1992. In 2021 we were recognized as a national innovation hub for advanced therapeutics and vaccines and have expanded our development capabilities to serve our clients. This includes a new development organization with cutting edge laboratories and technologies. We are now looking for a Scientist to join our Analytics team, at our Stockholm site, with starting date at the earliest convenience. You will be working with scientific tasks to prove that our analytical methods and equipment are suitable and functional as intended, e.g. validation and qualification. You will be working with method validation and analytical equipment qualifications to establish new methods and technology, as well as verification of existing methods (e.g. pharmacopeial methods) and requalification of equipment. As a contract manufacturer we are constantly adding new methods and equipment to our portfolio, often specialized to our customer needs, i.e. phase appropriate method validation. As such, broad experience from method validation and/or analysis of biologics is an advantage. Some of our main analytical methods are HPLC-based and HPLC experience is therefore highly meriting. We expect that applicants have a university degree of MSc within a relevant field for working in the Biopharmaceutical industry. For this recruitment we prefer an experienced candidates with 3+ years of experience from the pharmaceutical industry. Technical skills that are meriting are listed below. Technical skills Highly meriting Preferred Validation of analytical methods, especially for biologics Cell culture HPLC experience Cell-based assays Molecular biology methods (gels, qPCR, ELISA etc.) Basic microbiology Analytical equipment qualification Stability study planning and monitoring Lab incident, deviation, and OOS management Computerized systems qualification Examples of daily work tasks: Planning and reporting method validations. Planning, executing, and reporting analytical equipment qualifications. Troubleshoot existing protocols and methods. Support the team with expertise to enable development of robust methods. · Procurement commissioning and testing of analytical instruments. · Provide expertise to other departments. Participate in client projects and meetings. Plan tech transfers/method transfers from clients Support laboratory work in conjunction with method validation Routine QC laboratory work Risk assessments and change control. Lab incident, deviation, and OOS management. Tasks depending on individual expertise. The nature of the position is both administrative and, hands-on with analytical methods and equipment. A calm, technical and focused approach to scientific work is critical to succeed in this role. You must be able to demonstrate strong written and verbal communication skills and be fluent in English and Swedish. We are small and highly collaborative group, and you are expected to bring a positive force to the team and be prepared to assist where needed.