TOBLOR Consulting AB jobb

Camurus är ett internationellt forskningsbaserat läkemedelsföretag med fokus på utveckling och marknadsföring av differentierade och innovativa läkemedel för att förbättra livet för patienter med svåra och kroniska sjukdomar. Produkterna baseras på den unika formuleringsteknologin FluidCrystal® samt en omfattande expertis inom alla faser av läkemedelsutveckling. Utvecklingsportföljen innehåller produkter för behandling av beroende, smärta, cancer och endokrina sjukdomar. Camurus har verksamhet i Europa, USA och Australien, med huvudkontor i Lund, Sverige. Bolagets aktier är noterade på Nasdaq Stockholm under kortnamnet ”CAMX”. För mer information, se www.camurus.com och LinkedIn. Camurus befinner sig i en stark tillväxtfas och vi söker nu en Facility Director med övergripande ansvar för bolagets fastigheter, arbetsplatser och tillhörande servicetjänster. Det här är en nyckelroll för dig som vill kombinera strategiskt ansvar med ett nära och operativt ledarskap i en dynamisk organisation. Som Facility Director får du ett brett helhetsansvar för Camurus lokaler och arbetsplatser i Sverige, med huvudkontoret i Lund som bas. Du ansvarar för att skapa välfungerande, säkra och effektiva arbetsplatser och för att utveckla de facility-relaterade delarna av verksamheten i takt med att Camurus fortsätter att växa. Camurus har höga hållbarhetsambitioner och du kommer spela en nyckelroll i att omsätta dessa i praktiken inom ditt ansvarsområde. Rollen spänner från långsiktig planering, expansion och leverantörsstrategi till mer operativa frågor kring fastigheter, kontor och service. Du ansvarar för relationerna med fastighetsägare och externa leverantörer samt för upphandling och avtal inom exempelvis lokalvård, kontors- och laboratorieförnödenheter och andra arbetsplatsrelaterade tjänster. Hållbarhets- och effektivitetsfokus är naturliga delar av uppdraget. Du leder ett mindre team bestående av Facility Manager, Office Coordinator och Administrator och rapporterar till CFO. Rollen innebär också nära samarbete med bland annat IT, Sustainability och andra interna funktioner. Huvudsakliga ansvarsområden: · Leda, utveckla och koordinera facility- och officeorganisationen. · Ansvara för den dagliga driften samtidigt som du utvecklar området ur ett mer långsiktigt och strategiskt perspektiv. · Driva facility-relaterade frågor kopplade till Camurus tillväxt, expansion och framtida lokalbehov. · Ansvara för upphandling, förhandling och uppföljning av leverantörer och avtal inom facility och office services. · Ansvara för relationer och löpande dialog med fastighetsägare. · Övergripande ansvar för säkerhet, arbetsplatssäkerhet och brandskydd. · Arbeta med kostnadseffektivisering och hållbarhetsfrågor inom ansvarsområdet. Din profil Vi söker dig som har gedigen erfarenhet av Facility Management och är van vid ett brett ansvar för fastigheter, arbetsplatser och externa leverantörer. Du har erfarenhet av upphandling, avtal och förhandlingar med exempelvis fastighetsägare och serviceleverantörer och har förmågan att se både helheten och de operativa detaljerna. Du har gärna arbetat i en större organisation och har erfarenhet av att utveckla facility-verksamheten i samband med tillväxt, förändring eller expansion. Erfarenhet från läkemedels-, Life Science- eller livsmedelsindustrin är meriterande, eftersom förståelse för laboratoriemiljöer, reglerade verksamheter och de krav som följer med dessa är värdefullt i rollen. Du har också erfarenhet av att driva lokal- och ombyggnadsprojekt, från behovsanalys och upphandling till genomförande och inflyttning. Du har god kunskap om arbetsmiljö, arbetsplatssäkerhet och systematiskt brandskyddsarbete (SBA) och är van vid att omsätta krav och regelverk i praktiska rutiner. Du har ledaregenskaper och tycker om att utveckla människor och skapa ett välfungerande team. Samtidigt är detta en operativ chefsroll där du behöver trivas med att själv vara involverad i verksamheten och ta ansvar från början till slut. Rollen skulle även kunna passa dig som är redo att ta nästa steg till ett bredare chefsansvar. Som person är du pragmatisk, kommunikativ och serviceorienterad. Du har lätt för att skapa förtroende och relationer och kan samtidigt ställa krav när det behövs. Du är prestigelös och handlingskraftig, har ett tydligt ägarskap och en förmåga att prioritera och skapa framdrift även när många frågor pågår parallellt. Du behärskar svenska och engelska obehindrat i tal och skrift. B-körkort är ett krav. Camurus erbjuder Det här är en möjlighet att komma in i ett företag i en spännande fas av fortsatt tillväxt. Facility Director är en ny och bred roll där du får möjlighet att vara med och forma både tjänsten och hur facility-området ska utvecklas framåt. Camurus expansion innebär nya behov, nya lokaler och en organisation i förändring. Du får därför en viktig roll i bolagets fortsatta utveckling och stora möjligheter att påverka hur framtidens arbetsplatser och facility-funktion ska utformas. Camurus har närmare 300 medarbetare, varav drygt hälften är baserade i Sverige, med huvudkontor i Lund. Företagskulturen präglas av värderingarna innovation, collaboration, ownership, quality och passion. Information och ansökan För mer information om tjänsten är du välkommen att kontakta rekryteringskonsult Tobias Lorentzon på TOBLOR Consulting, telefon +46 735 11 10 60. Du söker tjänsten via TOBLOR Consultings karriärsida genom att registrera ditt CV och personliga brev. Urval och intervjuer sker löpande och vi ser därför gärna att du skickar in din ansökan så snart som möjligt. Vi ser fram emot din ansökan!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role, you will get the opportunity to work in a broad and independent quality position, close to both internal functions and external partners. Camurus is a rapidly growing and international company, and you will play an important role in ensuring quality and compliance throughout the supply and distribution network. Always with the patient in mind. We are looking for an experienced Senior Quality Assurance Manager to join our Quality organization at Camurus headquarters in Lund. This is a broad and independent role where you will work with quality assurance across Camurus' external supply and distribution network. You will have a key responsibility for quality agreements and quality aspects of supplier qualifications and monitoring, as well as for planning and conducting GDP and GMP audits. You will work closely with suppliers, distributors and other external partners, as well as with colleagues across the Camurus organization. The role combines hands-on quality work with a broader responsibility for ensuring that processes and external partners comply with Camurus' Quality Management System and applicable regulatory requirements. Your responsibility: · Independently review, establish, negotiate and maintain Quality Technical Agreements (QTAs) with suppliers and distributors. · Plan, conduct and document supplier qualifications and periodic supplier assessments. · Plan and lead GDP and GMP audits of suppliers, distributors and other quality-critical partners, as well as internal audits. · Lead deviation investigations, change controls, risk assessments and quality improvement initiatives. · Provide quality and compliance support to the organization in matters related to GDP, GMP and regulatory requirements. · Participate in regulatory inspections · Ensure that quality processes are developed, maintained and followed in accordance with the Camurus Quality Management System. · Collaborate cross-functionally with relevant internal functions and external partners. Candidate profile We are looking for an experienced quality professional with approximately 7–10 years of experience from the pharmaceutical industry. You hold an academic degree in Pharmacy, Chemistry, Biotechnology or another relevant Life Science discipline. You have solid experience from working in a regulated pharmaceutical environment and a strong understanding of GDP and/or GMP. Experience as a Responsible Person (RP) or Qualified Person (QP) is considered a strong merit. You have documented experience of planning, conducting and reporting supplier and GDP/GMP audits, as well as supplier qualification and ongoing supplier monitoring. You are also experienced in reviewing, negotiating and maintaining quality agreements with external partners. A solid understanding of European pharmaceutical legislation and regulatory requirements is essential. Good understanding of US regulations and/or experience of regulatory requirements outside the EU is considered a strong merit, and experience in areas complementing traditional pharmaceutical regulation, such as combination products, is considered an advantage. As a person, you are independent and confident in making decisions within your area of responsibility. You have high integrity and a pragmatic, yet quality-driven approach. You enjoy working in a dynamic environment with several parallel activities and are flexible enough to quickly adapt when priorities change. At the same time, you are collaborative and enjoy working cross-functionally across different parts of the organization. Fluency in spoken and written English is required. Camurus offers This is a great time to join a highly dynamic company during an exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are to continue in the same way. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers a broad and independent quality role with significant interaction across the organization and with external partners. You will have great opportunities to influence how Camurus works with quality and compliance as the company continues to grow internationally. Camurus has 300 employees with the headquarters located in Lund. The corporate culture is driven by the core values of innovation, collaboration, ownership, quality, and passion for realizing a patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. Selection and interviews will be conducted on an ongoing basis, so we encourage you to submit your application as soon as possible. For more information about Camurus, please visit: www.camurus.com/. We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working closely with colleagues across multiple disciplines as well as external partners. We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team. This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations (CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and reviewing non-clinical documentation and representing Non-Clinical Development in product development teams. Main responsibility Among others, your responsibilities will include: · Develop toxicology strategies and non-clinical development plans. · Design and monitor outsourced GLP studies. · Select, manage and collaborate with international CRO partners. · Prepare and review toxicology reports and regulatory documentation. · Represent Non-Clinical Development in cross-functional development teams. · Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD). Candidate profile You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline. You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry. Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued. You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage. As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related activities. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. At Camurus you will get the opportunity to work with committed colleagues in a fantastic Regulatory Affairs team with good atmosphere and supportive colleagues. Camurus is an innovative company currently expanding and establishing in new markets. In this position you will be part of the Regulatory team, based at the headquarters in Lund. The team today consists of 15 colleagues working with regulatory affairs activities, covering all existing and potential Camurus markets. You will work in a deadline-driven and international environment requiring a high level of flexibility. This is a key position where you will support marketed products. You will get the chance to work with different markets like EU and rest of the world. You will lead critical regulatory activities, ensuring compliance and facilitating effective communication with health authorities. You will be expected to quickly become a working part of the team. Your responsibility: · Lifecycle and maintenance activities for marketed products. · Maintaining core labelling, preparing and maintaining local labelling. · Contributing to and leading health authority interactions. · Monitoring regulatory intelligence information on a regular basis. · Represent Regulatory Affairs (RA) in the cross-functional teams and drive the regulatory agenda, raise RA concerns and opportunities. Candidate profile We are looking for a candidate with at least 10 years professional pharma industry experience, and at least 5 years regulatory affairs experience, preferably from a global RA team working with US and EU markets. This means you have good understanding of relevant regulatory-related regulations and guidelines. You have a Bachelor or Master of Science degree. Excellent communication and documentation skills (oral/written) in English is required, together with project management skills. To be successful in this role, you need a structured and organised mindset with strong focus on details and time management. You are good at independently managing multiple ongoing projects, but at the same time you enjoy working in a team. Even though you are highly structured, you support change and can adapt to new conditions. We value a supportive and flexible “roll up the sleeves” attitude. You see solutions rather than problems and you possess a strong personal drive. We also believe you have the “maintenance mindset”, crucial for working with products already on the market. Camurus offers This is a great time to join a highly dynamic company during an exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are to continue in the same way. With a diversified project portfolio in different stages, the commercial potential is considerable. This position offers a fantastic opportunity to work in a competent and committed Regulatory team – where the laughter is never far away. Camurus has 300 employees with the headquarters located in Lund. The corporate culture is driven by the core values of innovation, collaboration, ownership, quality, and passion for realizing a patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: www.camurus.com/. We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role you will get the opportunity to work with committed colleagues in a collaborative team. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the way we work with our outsourced manufacturing activities. We are looking for an experienced Senior Outsourcing Manager to join our Manufacturing Operations team. In this role, you will be responsible for driving outsourcing programs for injectable pharmaceutical products to Contract Manufacturing Organizations (CMOs), with a particular focus on late-stage development projects. As Senior Outsourcing Manager, you will serve as the primary interface between Camurus and external manufacturing partners. This is a true Project Management role where you will ensure successful project execution from technology transfer through start of commercial production. You will work closely with internal stakeholders and external partners to secure reliable, compliant, and efficient delivery of the project. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Develop and manage project plans, timelines, and milestones for technology transfer, process development, process validation, and manufacturing readiness activities together with CMO partners. · Drive day-to-day collaboration with CMOs and ensure agreed deliverables, timelines, and performance targets are achieved. · Lead operational meetings and steering committee meetings with external manufacturing partners. · Identify risks and issues proactively and drive mitigation and resolution activities together with internal and external stakeholders. · Coordinate and manage changes with CMOs, ensuring proper documentation, implementation, and alignment with project plans and contractual commitments. · Collaborate closely with internal Camurus functions such as Quality, R&D, Regulatory Affairs and Supply Chain to ensure successful project execution. · Ensure manufacturing activities are conducted in accordance with applicable GMP requirements and regulatory expectations. · Support continuous improvement initiatives related to outsourcing, external manufacturing operations, and CMO performance. Candidate profile We are looking for a professional with extensive experience from pharmaceutical manufacturing operations including outsourcing and CMO management. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have a solid understanding of GMP-regulated manufacturing environments and a proven track record of managing outsourcing programs and external manufacturing partners within the pharmaceutical or biotech industry. Experience from late-stage development, technology transfer and commercial manufacturing is highly valued. Experience from injectable products and combination products is considered a strong merit. As a person, you are structured, collaborative, and communicative, with a proven ability to drive complex projects and build strong relationships across multiple stakeholders. You combine a proactive and results-oriented mindset with a pragmatic and hands-on approach, while maintaining a humble and low-prestige attitude. Fluency in spoken and written and English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role, you will get the opportunity to work with committed colleagues in a collaborative team, close to both commercialised products and development projects. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the outsourced manufacturing processes throughout the product lifecycle. We are looking for an experienced Senior Process Engineer to join our Manufacturing Operations team. In this role, you will be responsible for leading technology transfer activities for manufacturing processes for injectable pharmaceutical products, from development into manufacturing environments at Contract Manufacturing Organizations (CMOs). You will support products from clinical development through to commercial supply. As Senior Process Engineer, you will act as a subject matter expert in pharmaceutical manufacturing processes, working closely with internal stakeholders and external partners to ensure robust, scalable, and GMP-compliant manufacturing operations. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Lead technology transfers of injectable pharmaceutical products from development into commercial manufacturing at CMOs. · Partner with R&D to ensure that formulation and process development activities support successful scale-up, manufacturability, and long-term process robustness. · Provide technical support for process development, scale-up, validation, and commercial manufacturing activities at CMOs. · Act as technical lead for investigations and troubleshooting of process deviations, OOS results, manufacturing failures, and other complex technical challenges. · Contribute to CMC documentation in support of global regulatory submissions and product lifecycle management. · Ensure that manufacturing processes are executed in accordance with applicable GMP requirements and regulatory expectations. Candidate profile We are looking for a professional with at least 7 years of experience from pharmaceutical manufacturing operations. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have hands-on experience from manufacturing process development, technology transfer, and GMP-regulated pharmaceutical manufacturing, preferably within sterile or injectable products. Experience from fill-finish operations and combination products development is considered a strong merit. As a person, you are collaborative, responsible, and driven by solving problems. You enjoy getting to the bottom of complex technical challenges and you are a pragmatic team player who takes ownership and follows through on commitments. At the same time, you are humble and low-prestige, always willing to support colleagues and contribute wherever needed. You thrive in a dynamic environment where technical expertise, collaboration, and problem-solving go hand in hand. Fluency in spoken and written English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

We enable a smarter, safer world by creating innovative solutions for improving security and business performance. As a network technology company and industry leader, we offer solutions in video surveillance, access control, intercom, and audio systems, enhanced by intelligent analytics applications. With around 6000 committed employees in over 50 countries, we collaborate with partners worldwide. Together, we thrive in our friendly, open, and collaborative culture and inspire each other to think beyond the expected. United by our commitment to inclusion, diversity, and sustainability, we consistently seek to develop our skills and way of working. Are you a hands-on leader with a passion for technology, industrial systems, and people? Do you enjoy building strong engineering teams and driving continuous improvement in a high-tech manufacturing environment? At Axis, you'll lead a team responsible for developing and maintaining the advanced equipment that powers the production of world-leading network video products. We are now looking for a Hardware Manager to join Production Engineering & Technology (PET) at our headquarters in Lund. Who is your future team? You will lead a team of 12 engineers working across mechanical and electronics development, focused on the machines and systems that power Axis production. This includes everything from optical alignment solutions to other advanced manufacturing equipment. The systems you’ll work with often combine motion, control, and precision — motors, sensors, and electrical cabinets are central building blocks. The team uses Creo for mechanical development, Windchill for documentation and E-plan for electrical design. You’ll work closely with software, QA, and industrialization teams, playing an important role in shaping how we develop and improve our production capabilities. As part of the PET management team, you collaborate with managers, product owners, and project leaders to align priorities, drive improvements, and ensure our global manufacturing runs smoothly. What will you do? You’ll lead your team both strategically and operationally, with focus on: • Setting direction, goals, and priorities for the group • Driving continuous improvement in tools, processes, and ways of working • Coaching and developing your team • Resource planning, recruitment, and performance management • Budget responsibility and delivery follow-up • Contributing to the broader PET management agenda Who are we looking for? We’re looking for a structured and pragmatic leader who combines technical curiosity with a genuine interest in developing people. You create clarity, build trust, and know how to engage a team around common goals. At the same time, you are comfortable making decisions, driving change, and challenging established ways of working when needed. You bring a solid technical foundation and know how to create structure and momentum in a team. You likely have: • A degree in mechanical engineering, electrical engineering, mechatronics, or similar • Several years of experience leading hardware or cross-functional engineering teams • Experience from industrial systems involving electronics, mechanics, and motion • Familiarity with tools such as Creo, PLM systems like Windchill, E-plan or Xpedition, • Strong communication skills in Swedish and English Technical environment Creo, Windchill, E-plan, Xpedition industrial control systems, motors, sensors, and electrical cabinets. What Axis has to offer We are a world leader in network video, where cutting-edge technology meets global impact. Here, you’ll contribute to meaningful projects that shape the future of security and surveillance — developing solutions used worldwide. Axis is a company where technology, innovation, and people development go hand in hand. Decisions are made close to the business, and leaders are trusted to take ownership. As a fast-growing company, we offer exciting career opportunities. You’ll grow professionally through continuous learning, supported by a collaborative team that values creativity, innovation, and work-life balance. Our Lund HQ Campus, including the impressive Grenden building, offers a dynamic environment with spaces crafted to encourage collaboration, whether through informal “fika” chats, formal meetings, or after-hours activities. Check it out: Axis HQ. Your well-being matters to us. We offer a range of benefits, including a company bonus, Friday cake, wellness allowance, health insurance — and even your own Axis bicycle. To learn more about Axis, our innovative products, solutions, and vibrant company culture, explore: Life at Axis blog Engineering at Axis blog Innovation at Axis  Ready to act? Axis is a company realizing the benefits of a diverse workforce. We know that diversity in groups creates a better working environment and promotes creativity, something that is fundamental for our success. We welcome all applications. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. Don’t hesitate to apply now, even though interviews will be held in August. We are looking forward to seeing your application!