Magle Chemoswed AB jobb

We are deeply passionate about shaping the future of medical solutions and contributing to healthcare's evolution. Magle Group is a multinational group headquartered in Malmö, South of Sweden, our team consist of 85 highly skilled professionals with diverse expertise and backgrounds. Regardless of what area of expertise, we all share the passion is to improve the lives of patients worldwide and we are committed to do an impact every day with our work. Do you want to be in the forefront of revolutionizing cellular production and opening doors to new possibilities in healthcare? If you like to work in an innovative team and be part of creating the future of cellular engineering, then we hope you apply for the below position. Responsibilities: We are developing the business and are looking for a Cell/Biochemical Engineer who can join our team to support our business in the ATMP /stem cell area where we are commercializing novel treatments and act as CDMO. We consider our customers as partners and together we make it possible to provide ATMP (Advanced Therapy Medical Products) to patients in need. We work together with life science companies, universities and hospitals and produce ATMP in a GMP environment. You will work in a high standard GMP facility with “state-of-the-art” equipment. Our team is growing and we consider applications with seniority as well for someone that is in the start of their career. Designing and optimizing cellular production processes. Conducting research to enhance cell viability, productivity, and efficiency. Collaborating with cross-functional teams to develop and find solutions. Implementing quality control measures to ensure product integrity. Contributing to the advancement of scientific knowledge through publications and presentations. Requirements: Degree- Cell Biology, Biochemistry, Chemical Engineering, or related field. Proven experience in cellular engineering, including cell culture techniques, metabolic engineering, and molecular biology. Experience from working in a GMP environment. Excellent collaboration skills, you will work internally with multidisciplinary teams as well with our external partners. Excellent communications skills, both orally and in writing – our cooperate language is English. How to Apply: If you are passionate about making a meaningful impact in the field of healthcare and feel the above position fits your experience, we would love to hear from you. We will have an continuous recruitment process for this position and would like to have your application as soon as possible however no later than the 19th of April.Please submit your CV and a short cover letter telling us a bit more about you. This position will be place in Lund and will be a full-time position. To find out more about us please visit our group Webb page. www.maglegroup.com.

Magle Group is a dynamic company within in the pharma industry. We are a team of 80 dedicated professionals with different areas of expertise, we have the total value chain from early development to large scale manufacturing. Working at Magle means you make an impact for others, we are culture driven company, always aware that our work improves the living conditions for patients around the world. To learn more about us visit: https://maglegroup.teamtailor.com/ We are looking for you who wants to take a first step towards working as a legal counsel and who is interested in working close to business. We look for a highly motivated person that naturally takes ownership and is at the end of your studies or in the beginning of your career and are eager to explore how it is to work as a legal counsel within a company where you will support a diverse range of legal matters and gain valuable experience in company environment. The position is a vacancy position that will last until April 2025 since our legal counsel will be on parental leave. Position Overview: As a Junior Legal Counsel at Magle, you will play a key role in supporting the organization in legal matters. This position offers a unique blend of responsibilities, allowing you to gain exposure to various aspects of legal practice within a business setting. You will be preparing legal documents, maintaining filings, liaising with authorities, taking charge of the secretarial work for the Board. creating presentations for board meetings and providing valuable legal advice to support our business operations. Key Responsibilities: Legal Document Preparation: Draft, review, and finalize legal documents, ensuring accuracy and compliance with relevant laws and regulations. Filing and Compliance: Manage and maintain organized legal files, ensuring the company's compliance with all applicable laws and regulations, including rules applicable to the listing environment. Government Authorities Liaison: Establish and maintain effective communication with relevant government authorities, ensuring timely and accurate submissions. Board Meeting Support: Prepare and present legal documents and presentations for board meetings, collaborating with other departments to provide comprehensive insights. Business Advisory: Provide legal support and advice to different business units, helping navigate legal issues and contributing to informed decision-making. Agreement Management: Review, draft, and negotiate agreements with partners, both customers and suppliers, ensuring the company's interests are protected. Legal Research: Stay updated on legal changes and developments that may impact the company, and communicate relevant information to the team. Qualifications: Jur kand (LLM) degree or equivalent degree within the field of law/business law Strong organizational and multitasking skills. Excellent communication and interpersonal abilities. Detail-oriented with a commitment to producing high-quality work. Professional knowledge of English and Swedish Notary service or other experience from administrative work In this position you need to be able to structure your work and be able to prioritize. We need you to be organized and thorough and able finding information that can help you to give answers. We are in a fast-moving environment and there is a need that you are flexible and can adjust your work when needed. In this position you will work close to our CEO and the executive team at Magle and you need to be able to handle confidential information and have a high integrity. We will in this recruitment process place great emphasis on personal qualities. If you find the above position interesting, we want to get to know you. Please send us your CV and a short personal letter why you think this position would be a match for your aspirations. We will have a continuous recruitment process so please apply as soon as possible but no later than April 4th.

Are you an experienced QA Specialist that have a passion for quality? Do you love to work cross-over with other department and develop processes and find better, more efficient ways to work? Join us at Magle Chemoswed! You will play a key role in securing quality and thus enable us to bring life changing healthcare innovations to patients. We are an ambitions company that strive towards new ways of working in order to develop and improve to help patients in need. Having high quality products is key for our success. To succeed in the role of QA Specialist at Magle, you should enjoy working both independently and with others - strong collaboration and communication skills are crucial for this position. You should also feel comfortable in a changing environment and be able to adjust your work depending on the business needs. We look for someone who is organized, driven, efficient, and capable to explain and support the organization in quality matters. Key Responsibilities: - Responsible for reviewing batch documentation. - Release APIs, raw materials, and deliveries. - QA approval of Standard Operating Procedures (SOPs). - Manage changes, deviations, and complaints. - Provide customer support. - Participate in customer and regulatory inspections, investigations, and risk assessments. - QA encompasses a broad range of tasks, and there are opportunities for development in various areas. Requirements for the Position: - University degree in chemistry, pharmaceuticals, or equivalent engineering discipline. - Previous work experience in pharmaceutical or Medical Device operations according to GMP and ISO 13485 - Excellent proficiency in both Swedish and English, spoken and written, as both languages are used in the job. - Experienced user of Microsoft Office and a Q Management system - Experience in QA work for projects in clinical phases is highly advantageous. If you are passionate about making a meaningful impact and feel the above position fits your experience, we would love to hear from you. In this process we will have an continuous recruitment, please submit your CV and a short cover letter telling us why you find the position interesting. The position is placed at our office in Malmö and will be a full time position. To find out more about us please visit our group Webb page. www.maglegroup.com