Lediga jobb Mpya Sci & Tech AB i Solna

Are you known for your creative, pragmatic, and collaborative approach to work? Are you someone who thrives on turning challenges into opportunities? If so, we have an exciting opportunity for you to join Xbrane Biopharma as the responsible individual for our IT systems. Join us and become a part of a remarkable Swedish success story in the field of biopharmaceutical drug development.

The role

This presents a remarkable opportunity to join an exceptionally dynamic team and assume a vital role in the advancement of Xbranes' IT systems and processes. The primary focus of this position entails enhancing the existing ELN system to facilitate more secure and efficient interactions between equipment and individuals. Additionally, this role will serve as a liaison with suppliers, ensuring that procured products, both new and existing, align with Xbrane's stringent requirements.

A highly valued competency for this position involves the ability to lead projects and drive internal and external stakeholders toward streamlined and secure processes. While practical in nature, technical challenges may arise, necessitating a fundamental understanding and a keen interest in technical problem-solving skills are required. The individual in this role need not be a technical expert, but rather a project leader who guarantees the smooth and secure functioning of IT processes for Xbrane's continued progress. You will also be responsible for setting and securing practical and functional data management.

About you

We are seeking an IT enthusiast with a strong passion for technology and a deep understanding of its applications. The ideal candidate will have experience in project management and coordination, ensuring successful completion of tasks within specified deadlines. They should possess the ability to see the bigger picture and develop strategic plans to achieve organizational goals. Additionally, we value candidates who excel in building relationships, fostering collaboration, and have a keen interest in exploring innovative work methods. Knowledge and understanding of laboratory environments and processes is highly desirable. The successful candidate should demonstrate confidence, be driven forward by challenges, and showcase a curious and interested mindset.

• BSc, MSc or PhD degree in Life Sciences or related field, depending on experience.
• Experience with LIMS or ELN systems.
• At least 3 years of experience in pharmaceutical manufacturing and/or drug development.
• Proficient in English

Why Xbrane?

Xbrane is a Great Place to Work certified company that offers an opportunity to grow in your professional role, as well as to influence and further develop the company as a whole alongside a highly competent team.

If you have a can-do attitude and on top of that share our values, Make it happen, Beat yesterday, Impossible is nothing and We win as one, you will prosper with us.

Interested?
In this recruitment, Xbrane is collaborating with Mpya Sci & Tech. Please submit your application at www.mpyascitech.com no later than the 30th of June. Interviews will be scheduled continuously. Questions? Please contact Johan Östman, +46(0)76 628 78 91 or [email protected] Visa mindre

Are you an excellent project manager in pharmaceutical production? Do you get excited by perfect delivery performance? Do you have a flexible, creative, pragmatic, and collaborative approach at work? Do you turn challenges into opportunities? This is an exciting opportunity for you to join Xbrane Biopharma AB in Solna, a company developing Biosimilar products to make drugs accessible to less privileged populations globally!

As a Product Coordinating Manager in the Manufacturing and Supply Chain team at Xbrane Biopharma, you will be responsible for coordinating the work activities related to the new product introduction on the commercial market, including coordination of contract manufacturing organizations (CMOs), suppliers, and partners to ensure an efficient and reliable production supply chain from manufacturing to patients at all times.

You will work in a cross-functional team in close collaboration with R&D, QA, and Regulatory Affairs to secure sustainable and compliant commercial manufacturing processes for current and future needs, due to continuous product improvement, including the new market entrance. You report to Xbrane’s Head of Manufacturing and Supply Chain in this role.

Qualifications:

• University degree in Life Sciences with several years of experience within the pharma industry
• Extensive project management experience, including coordinating external activities and managing relationships with contractors or partners with great relation-oriented communication skills.
• Experience and knowledge in pharmaceutical manufacturing
• Experience from supply of products in commercial phase
• Interest in development and new introduction of the product to market
• Experience working under GMP requirements
• Proficient in English
• Additional experience with biopharmaceutical drug substance manufacturing, drug product manufacturing, and packaging and labeling processes is meriting.

The individual must be highly motivated, flexible and service minded. It is important to possess excellent communication and collaborative skills, providing strong support to the team with your analytical and problem-solving skills and expertise within pharmaceutical production.

For questions about the position, you are most welcome to contact Talent Advisor, Johan Östman at +46(0)76 628 78 91, or [email protected] Your application may be added no later than the 13th of March at www.mpyascitech.com

About Xbrane Biopharma

Xbrane Biopharma is a Swedish biotechnology company that develops and manufactures biosimilars. Xbrane has a patented protein production platform and world-leading expertise in biosimilar development. This is a Great Place to Work certified company with an entrepreneurial spirit that focuses on being creative, coming up with new ideas, and following a rigorous process to bring those ideas to fruition. Xbrane’s headquarter is located at Solna Campus, just outside of Stockholm, for more information see www.xbrane.com

At Xbrane, you contribute to creating an environment where we win as one! Solidarity and togetherness are key to our performance and well-being. You enjoy being part of a team sharing the same values and purpose, working together, and giving trust, recognition & support as we grow as one Xbrane family – at Xbrane you will never walk alone. Visa mindre

Xbrane Biopharma AB in Solna is an innovative company developing Biosimilar products to make drugs accessible to less privileged populations globally. This is an exciting opportunity to join an innovative and growing team within the development of Biosimilars.

You will be part of the Upstream Process Development (USPD) team responsible for generating mammalian cell lines for Xbrane’s pipeline and implementing new technologies and processes for continuous platform improvement. You will be working in a high-performing and collaborative environment to ensure that project goals and timelines are met and will have a direct impact on shaping Xbrane’s expression and cell line development platforms.

Responsibilities:

• Develop and implement Xbrane’s expression and cell line development (CLD) platform in collaboration with internal and external partners
• Technical oversight of the CLD platform (from vector construction to single clone selection and stability studies) and ensure that CLD work packages are delivered according to project timelines.
• Represent the CLD function on project teams, making decisions for CLD activities and effectively communicating results, progress, and plans.
• Author reports, process descriptions, and other documents
• Prepare and review cell culture-related project IND submissions and ensure compliance with regulatory requirements during development.
• Provide expertise, educate colleagues, and keep up to date in the field of CLD.
• Identify and resolve key technical issues during project development.

Qualification:

• PhD in a relevant Life Science discipline with a minimum of three years of relevant experience or Master’s degree with a minimum of five years of relevant experience.
• Hands-on experience in mammalian suspension cell culture (e.g., CHO, HEK293, NS0 and Sp2/0 cells) in a pharmaceutical or biotechnology setting.
• Strong technical background in vector construction, transfection, stable pool generation, single-cell cloning, cell bank generation and small-scale protein
• Technical expertise with molecular biology techniques and methods including gene design & modification, PCR/qPCR, DNA extraction and sequencing, transfection, chromosome integration, single-cell cloning and screening, gel electrophoresis & blotting and flow cytometry is highly desirable.
• Experience with monoclonal antibody production and biosimilar development is

You are well organized and possess great time-management skills. You are a team player with excellent communication, presentation and writing skills and you need to be fluent in English.

Xbrane is a Great Place to Work certified company that offers an opportunity to grow in your professional role, as well as the opportunity to influence and further develop the company as a whole alongside a highly competent team.

If you have a can-do attitude and on top of that share our values, Make it happen, Beat yesterday, Impossible is nothing and We win as one, you will prosper with us.

Interested?
In this recruitment, Xbrane is collaborating with Mpya Sci & Tech.

Please submit your application no later than the 23th of October. Interviews will be scheduled continuously. Questions? Please contact Johan Östman, +46(0)76 628 78 91 or [email protected]

About Xbrane Biopharma

Xbrane Biopharma is a Swedish biotechnology company that develops and manufactures biosimilars. Xbrane has a patented protein production platform and world-leading expertise within biosimilar development. This is a Great Place to Work certified company with an entrepreneurial spirit that focuses on being creative and coming up with new ideas as well as on following a rigorous process to bring those ideas to fruition. Xbrane’s headquarter is located at Solna Campus, just outside of Stockholm, for more information see www.xbrane.com. Visa mindre

Orkla Wound Care, en del av Orkla Care, söker sin nästa Head of Regulatory Affairs and Quality till sitt huvudkontor i Solna. Orkla Wound Care förser marknaderna med kvalitetssäkrade första hjälpen- och sårvårdsprodukter. Orkla Wound Care har sin produktion och huvudmarknad inom Europa men har idag en försäljning på över 40 marknader världen över. Några kända varumärken är bland annat Salvequick och Norgesplaster inom B2C, och Cederroth First Aid och Snögg inom B2B.

Om tjänsten

Orkla Wound Care har en Regulatory Affairs & Quality avdelning som består av fyra personer, till den söker man nu en Head of Regulatory Affairs & Quality. Gruppens övergripande ansvar är bland annat att säkerställa att produkterna som frisläpps till marknaden av Orkla Wound Care följer de regulatoriska kraven på varje produktkategori, varav merparten är medicintekniska produkter.

I rollen som Head of Regulatory Affairs & Quality har du ansvar för både den löpande verksamheten och utveckling av densamma. Du förväntas att på ett engagerat sätt utveckla och stötta medarbetarna samt bidra med expertis inom ISO 13485. Rollen innehåller både ledarskapsaktiviteter såsom utvecklingssamtal och arbetsfördelning samt operativa delar kring regulatory och QA såsom teknisk dokumentation, riskanalyser, avvikelser, post market surveillence och vigilance med mera.

Din profil
Vi söker dig som har:

• Akademisk utbildning inom kemi, teknik, biologi eller motsvarande
•
•
• Tidigare erfarenhet från QA och RA inom Medical Devices/Medtech?
•
•
• Tidigare erfarenhet som Team Leader eller motsvarande
•
•
• God erfarenhet inom regelverket ISO 13485 samt annat reglerande lagstiftning?
•
•
• God svenska och engelska i tal och skrift ?
•
•

Meriterande

• Kunskap och erfarenhet av utländska regelverk, även utanför EU.
•
•

Utöver att inneha goda ledaregenskaper behöver man som person vara flexibel och självgående samt vara strukturerad och bra på att prioritera. Stor vikt kommer att läggas vid personlig lämplighet.

Orkla Care erbjuder
Orkla Wound Care erbjuder en utvecklande roll där du jobbar med både ledarskapsuppgifter och med specialistfrågor. Du kommer till ett team med bred kompetens och får fördelarna med att jobba i det lilla bolaget inom det stora bolaget, exempelvis god överblick och korta beslutsvägar. Samtidigt är du i en global koncern med många möjligheter. Bolaget befinner sig i en tillväxtfas vilket bådar gott för framtida utvecklingsmöjligheter.

Tveka inte att ansöka redan idag om detta låter som ett spännande nästa steg för dig!

Har vi fångat ditt intresse?

I den här rekryteringen samarbetar Orkla Wound Care med Mpya Sci & Tech Har du frågor om tjänsten är du välkommen att kontakta rekryteringskonsult Ellinor Crafoord [email protected] 0721765167.

Obs! Orkla Wound Care vill tillsätta tjänsten snarast, så inkom med din ansökan snarast möjligt.

Vi ser fram emot din ansökan! Visa mindre

Orkla Wound Care, en del av Orkla Care, söker sin nästa Head of Regulatory Affairs and Quality till sitt huvudkontor i Solna. Orkla Wound Care förser marknaderna med kvalitetssäkrade första hjälpen- och sårvårdsprodukter. Orkla Wound Care har sin produktion och huvudmarknad inom Europa men har idag en försäljning på över 40 marknader världen över. Några kända varumärken är bland annat Salvequick och Norgesplaster inom B2C, och Cederroth First Aid och Snögg inom B2B.

Om tjänsten

Orkla Wound Care har en Regulatory Affairs & Quality avdelning som består av fyra personer, till den söker man nu en Head of Regulatory Affairs & Quality. Gruppens övergripande ansvar är bland annat att säkerställa att produkterna som frisläpps till marknaden av Orkla Wound Care följer de regulatoriska kraven på varje produktkategori, varav merparten är medicintekniska produkter.

I rollen som Head of Regulatory Affairs & Quality har du ansvar för både den löpande verksamheten och utveckling av densamma. Du förväntas att på ett engagerat sätt utveckla och stötta medarbetarna samt bidra med expertis inom ISO 13485. Rollen innehåller både ledarskapsaktiviteter såsom utvecklingssamtal och arbetsfördelning samt operativa delar kring regulatory och QA såsom teknisk dokumentation, riskanalyser, avvikelser, post market surveillence och vigilance med mera.

Din profil
Vi söker dig som har:

• Akademisk utbildning inom kemi, teknik, biologi eller motsvarande
•
•
• Tidigare erfarenhet från QA och RA inom Medical Devices/Medtech?
•
•
• Tidigare erfarenhet som Team Leader eller motsvarande
•
•
• God erfarenhet inom regelverket ISO 13485 samt annat reglerande lagstiftning?
•
•
• God svenska och engelska i tal och skrift ?
•
•

Meriterande

• Kunskap och erfarenhet av utländska regelverk, även utanför EU.
•
•

Utöver att inneha goda ledaregenskaper behöver man som person vara flexibel och självgående samt vara strukturerad och bra på att prioritera. Stor vikt kommer att läggas vid personlig lämplighet.

Orkla Care erbjuder
Orkla Wound Care erbjuder en utvecklande roll där du jobbar med både ledarskapsuppgifter och med specialistfrågor. Du kommer till ett team med bred kompetens och får fördelarna med att jobba i det lilla bolaget inom det stora bolaget, exempelvis god överblick och korta beslutsvägar. Samtidigt är du i en global koncern med många möjligheter. Bolaget befinner sig i en tillväxtfas vilket bådar gott för framtida utvecklingsmöjligheter.

Tveka inte att ansöka redan idag om detta låter som ett spännande nästa steg för dig!

Har vi fångat ditt intresse?

I den här rekryteringen samarbetar Orkla Wound Care med Mpya Sci & Tech Har du frågor om tjänsten är du välkommen att kontakta rekryteringskonsult Ellinor Crafoord [email protected] 0721765167.

Vi ser fram emot din ansökan! Visa mindre

Atlas Antibodies develops, produces, markets and sells advanced reagents for biomedical research. The company originates from the Swedish-based Human Protein Atlas project and was founded in 2006 by researchers at the Royal Institute of Technology (KTH) and the Rudbeck Laboratory / Uppsala University. The company offers four high-quality product lines: Triple A Polyclonals ™, PrecisA Monoclonals ™, PrEST Antigen ™, and QPrEST ™ standards for absolute quantification of proteins using mass spectrometry. Atlas Antibodies is based in Stockholm, has around 70 employees and markets and sells its products globally through several distribution channels.

Read more on the company website: www.atlasantibodies.com

Atlas Antibodies is a cutting-edge biotechnology company with strong growth, exciting products and an interesting history built on a solid R&D heritage from the Human Protein Atlas project. Atlas Antibodies is a company with great opportunities as it comprises the entire product chain, from research and development to production as well as sales and marketing. Atlas Antibodies has sites in Stockholm, Switzerland and England. At the Stockholm site works approximately 80 colleagues and the team is constantly growing.

Atlas Antibodies is now looking for a Senior Transformation and Quality Manager passionate about creating value for customers to lead our transformation, project management and quality team. The Sr Transformation and Quality Manager reports to the CEO and will play a crucial role in the strategic and tactical development of the company.

The role:

This is an opportunity to work on operative level, both with everyday tasks and on strategic level, with input to the business development of the company. You will lead our improvement work and project management office. You will interact and collaborate with all functions at Atlas Antibodies Solna, as well as with several functions within the global organization. Your responsibilities also include:

• Lead a team consisting of project managers and quality officers that will report to you. You will also be part of the Atlas Antibodies Leadership Team.
• Lead continuous improvement team while staying hands-on champion
• Direct, lead and facilitate the ongoing continuous improvement process with techniques such as Kaizen, Problem Solving, Daily Management etc.
• Identify ongoing lean improvement training needs and assist with developing and implementing the required training.
• Provide leadership and direction needed to ensure that regulations are followed, quality management systems are implemented and followed.
• Development and maintenance of the QMS. Prepare for and lead the site in external audit execution and be responsible for internal audits

Qualifications:

To succeed in this role, we think that you have a few years’ experience of working with change management and improvements in a multifunctional organization. You have a life science industry background with experience of working with regulatory frameworks (e.g. IVD-R), EHS regulations and sustainability practices.

• Experience in change management and understanding of continuous improvement using lean tools like Six Sigma and value stream mapping.
• Hands-on experience in designing and implementing Lean solutions and framework of continuous improvement
• Experience in designing remediation plans to address gaps, lead/support problem solving, and track record of following through to ensure closure.
• Excellent verbal and written communication skills and the ability to interact professionally with a diverse group of peers, senior managers, and subject matter experts.
• Strong analytical, project and product management skills, including a thorough understanding of how to interpret business needs and translate them into operational requirements.
• Bringing people together and aligning them around common goals.
• Results-oriented: take personal accountability to deliver results.
• Problem-solving skills. Able to find solutions to difficult or complex issues.
• A ‘completer-finisher’ taking accountability for ideas from inception to delivery, in an environment that requires robust metrics to confirm success.
• Fluent in English, verbally and written, Swedish is meritorious.

We offer you the unique combination of a critical and challenging role and a creative and empowering environment. You will be actively encouraged to make improvements and have a direct impact on the success of Atlas Antibodies as well as build and position the role and its important mission. Furthermore, you will have excellent opportunities to build your career in our fast-growing organization.

Interested?

In this recruitment, Atlas Antibodies is collaborating with Mpya Sci & Tech. Please submit your application as soon as possible and no later than 16th of January. If you have any questions regarding the recruitment process or about this role, you are welcome to contact Johan Östman, 076-628 78 91 or at [email protected]

Atlas Antibodies is stemming from the Human Protein Atlas and is built on a solid foundation where innovative and creative mindsets are combined with the latest techniques and technology. Our culture is one that empowers individuals to work together as a team, and our coworkers are responsible and passionate. Welcome to be a part of a unique company, with strong growth, where you will get the opportunity to work in a research-driven atmosphere in which R&D comprises an important part of the company. For more information please visit: www.atlasantibodies.com Visa mindre

Xbrane Biopharma AB in Solna is an innovative company developing Biosimilar products. There are approximately 60 people working at Xbrane and 8 at the Manufacturing & Supply Chain department. By joining Xbrane, you will be part of a biopharmaceutical drug development company with the goal to ensure the access of biologics to an underserved patient population, enabling global health equality.

Xbrane is expanding and will be releasing a new product in the upcoming year. As the Transport Coordinator your main task will be to book, oversee and coordinate transports of mainly refrigerated and sensitive substances/pharmaceuticals within Europe and the US. Your responsibility is to ensure that deliveries between contract manufacturers, analysis laboratories etc., arrives safely and on time, is correctly documented, and to prevent and solve any issues that may arise at customs/border controls or elsewhere during transport.

Responsibilities:

• To keep a close dialogue with carriers contracted to perform transports on behalf of Xbrane

• Have close communication with external partners handling transports at contract manufacturers, analysis laboratories etc.
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• To plan and coordinate transports in dialogue with the internal Xbrane team being in daily contact with contract manufacturers and analysis laboratories etc.
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• To issue and ensure that all the necessary documentation is in order to prevent deliveries getting stopped at customs/border controls and to ensure full traceability for each transport
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• To collect, review and file data from temperature loggers
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• To report and investigate transport deviations in cooperation with the quality department, when necessary

You will have a close dialogue and interaction with the internal team in your daily work. Continuous improvement work will also be relevant since this is a new position/role within the department.

Qualifications:

• 2-3 years previous experience as a transport coordinator/planner, preferably within the life science industry
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• GDP or equivalent experience/knowledge
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• High proficiency in English, since most documents and communication is in English

Other valued qualifications are previous work experience with dealing with customs, coordinating transports across borders and previous experience with refrigerated and sensitive substances/pharmaceuticals.

To succeed in this role, we see that you are a flexible, curious and well organized person. You have a mind for quality and planning and can work efficiently both independently and in teams, and you regard yourself as a problem solver. It is also important that you are service minded since internal and external communication is a big part of the daily tasks.

Xbrane is a Great Place to Work certified company that offers an opportunity to grow in your professional role, as well as the opportunity to influence and further develop the company as a whole alongside a highly competent team.

If you have a can-do attitude and on top of that share our values; Make it happen, Beat yesterday, Impossible is nothing and We win as one, you will prosper with us.

Interested?

Please submit your application no later than 24th of October. Contact Talent Advisor Johan Östman at +46766287891 or [email protected] for further questions. Please note that we interview candidates continously and the position may be filled before last application date so apply today!

About Xbrane Biopharma

Xbrane Biopharma is a Swedish biotechnology company which develops and manufactures biosimilars. Xbrane has a patented protein production platform and world-leading expertise within biosimilar development. This is a Great Place to Work certified company with an entrepreneurial spirit that focuses on being creative and coming up with new ideas as well as on following a rigorous process to bring those ideas to fruition. Xbrane’s headquarter is located at Solna Campus, just outside of Stockholm, for more information see www.xbrane.com. Visa mindre