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Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.

Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care

As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your responsibilities will include preparing the organization for audits and conducting supplier audits.

At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an active life.

We will interview candidates continuously and welcome your application today!

The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality perspective. You will report directly to the Director of QA/RA at Inossia.

Your main responsibilities will include:

• Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical device regulations

• Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release, and post-market activities

• Oversee risk management activities, including risk files, benefit-risk analysis, and lifecycle updates

• Plan, conduct, and support internal and external audits, including notified body, supplier, and regulatory audits

• Act as a key point of contact for audit readiness, responses, and corrective actions

• Manage CAPA, non-conformances, deviations, and change control processes

• Collaborate cross-functionally to ensure quality is embedded across the organisation

• Support supplier quality management, qualification, and ongoing performance monitoring

• Ensure robust documentation control, version management, and data integrity

• Contribute to key strategic developments within the QA department.

Key Qualifications for the position include:

• Multiple years of QA experience within the medical device industry, preferably in a smaller-sized company

• Strong hands-on knowledge of ISO 13485 and ISO 14971

• Proven experience leading and supporting audits and inspections

• Solid understanding of medical device quality systems, risk management, and product development processes

• Experience working in cross-functional, international environments

• Fluency in English, both in speaking and in writing

We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a positive impact.

If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role, we invite you to apply today!

Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.

Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care

• Inossia has completed a clinical study of 196 patients in 4 countries and 9 clinics

• Inossia received the Breakthrough Device Designation for Inossia Cement Softener in June 2025

To learn more, please visit www.Inossia.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.

Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care

As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your responsibilities will include preparing the organization for audits and conducting supplier audits.

At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an active life.

We will interview candidates continuously and welcome your application today!

The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality perspective. You will report directly to the Director of QA/RA at Inossia.

Your main responsibilities will include:

• Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical device regulations

• Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release, and post-market activities

• Oversee risk management activities, including risk files, benefit-risk analysis, and lifecycle updates

• Plan, conduct, and support internal and external audits, including notified body, supplier, and regulatory audits

• Act as a key point of contact for audit readiness, responses, and corrective actions

• Manage CAPA, non-conformances, deviations, and change control processes

• Collaborate cross-functionally to ensure quality is embedded across the organisation

• Support supplier quality management, qualification, and ongoing performance monitoring

• Ensure robust documentation control, version management, and data integrity

• Contribute to key strategic developments within the QA department.

Key Qualifications for the position include:

• Multiple years of QA experience within the medical device industry, preferably in a smaller-sized company

• Strong hands-on knowledge of ISO 13485 and ISO 14971

• Proven experience leading and supporting audits and inspections

• Solid understanding of medical device quality systems, risk management, and product development processes

• Experience working in cross-functional, international environments

• Fluency in English, both in speaking and in writing

We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a positive impact.

If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role, we invite you to apply today!

Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.

Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care

• Inossia has completed a clinical study of 196 patients in 4 countries and 9 clinics

• Inossia received the Breakthrough Device Designation for Inossia Cement Softener in June 2025

To learn more, please visit www.Inossia.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines.

Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio.

We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us!

Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today!

As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance.

Duties and responsibilities include:

• Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase

• Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products

• Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release

• Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making.

• Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues

• Participating in budget planning and monitoring

• Ensure compliance with global regulatory requirements and support regulatory inspections and audits

The suitable candidate has the following qualifications:

• Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry

• Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry

• Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods)

• Expert knowledge in analytical and/or process development for biologics

• Understanding of supply planning and supplier management

• Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills

• Is analytical, solution-oriented with a strong personal drive

• Is structured and organized

• Has a good eye for detail and a thorough approach to work

• Is a proactive, flexible, motivated and ambitious team player with ability to drive change

If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead!

Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines.

Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio.

We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us!

Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today!

As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance.

Duties and responsibilities include:

• Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase

• Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products

• Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release

• Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making.

• Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues

• Participating in budget planning and monitoring

• Ensure compliance with global regulatory requirements and support regulatory inspections and audits

The suitable candidate has the following qualifications:

• Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry

• Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry

• Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods)

• Expert knowledge in analytical and/or process development for biologics

• Understanding of supply planning and supplier management

• Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills

• Is analytical, solution-oriented with a strong personal drive

• Is structured and organized

• Has a good eye for detail and a thorough approach to work

• Is a proactive, flexible, motivated and ambitious team player with ability to drive change

If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead!

Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.

Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care

As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your responsibilities will include preparing the organization for audits and conducting supplier audits.

At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an active life.

We will interview candidates continuously and welcome your application today!

The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality perspective. You will report directly to the Director of QA/RA at Inossia.

Your main responsibilities will include:

• Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical device regulations

• Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release, and post-market activities

• Oversee risk management activities, including risk files, benefit-risk analysis, and lifecycle updates

• Plan, conduct, and support internal and external audits, including notified body, supplier, and regulatory audits

• Act as a key point of contact for audit readiness, responses, and corrective actions

• Manage CAPA, non-conformances, deviations, and change control processes

• Collaborate cross-functionally to ensure quality is embedded across the organisation

• Support supplier quality management, qualification, and ongoing performance monitoring

• Ensure robust documentation control, version management, and data integrity

• Contribute to key strategic developments within the QA department.

Key Qualifications for the position include:

• Multiple years of QA experience within the medical device industry, preferably in a smaller-sized company

• Strong hands-on knowledge of ISO 13485 and ISO 14971

• Proven experience leading and supporting audits and inspections

• Solid understanding of medical device quality systems, risk management, and product development processes

• Experience working in cross-functional, international environments

• Fluency in English, both in speaking and in writing

We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a positive impact.

If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role, we invite you to apply today!

Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.

Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care

• Inossia has completed a clinical study of 196 patients in 4 countries and 9 clinics

• Inossia received the Breakthrough Device Designation for Inossia Cement Softener in June 2025

To learn more, please visit www.Inossia.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines.

Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio.

We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us!

Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today!

As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance.

Duties and responsibilities include:

• Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase

• Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products

• Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release

• Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making.

• Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues

• Participating in budget planning and monitoring

• Ensure compliance with global regulatory requirements and support regulatory inspections and audits

The suitable candidate has the following qualifications:

• Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry

• Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry

• Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods)

• Expert knowledge in analytical and/or process development for biologics

• Understanding of supply planning and supplier management

• Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills

• Is analytical, solution-oriented with a strong personal drive

• Is structured and organized

• Has a good eye for detail and a thorough approach to work

• Is a proactive, flexible, motivated and ambitious team player with ability to drive change

If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead!

Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

We are looking for a Planning and Cost Controlling Engineer to join our project management team in Northern Sweden. Please find the required qualifications and job description below.

• A bachelor’s degree in Civil Engineering, Industrial Engineering or Mechanical Engineering is required.
• Additional training or specialization in Project Management or Cost Control.
• Minimum 5 years of relevant experience in project estimating and cost control.
• Proven experience in the successful delivery of complex, multi-interface projects, including creating baselines, analyzing activities, critical path and float control, and defining logical relationships.
• Experience in large scale projects and working within planning and cost control teams.
• Strong technical skills in project cost planning, scheduling, and reporting.
• Proficiency in Primavera P6 is mandatory.
• Strong interpersonal, communication, and presentation skills.
• Proficiency in Excel, including S-curve progress calculations.
• Strong analytical and problem-solving capabilities with excellent attention to detail.
• Solid project background with strong technical writing skills.
• Mature, proactive, resourceful, hands-on, and self-driven.
• Ability to work independently with minimal supervision.
• Control and monitor total project expenditure, including verification and checking of invoices and claims from suppliers, vendors, and subcontractors, ensuring all costs are accurately recorded.
• Provide planning and cost control support across all project phases, including variation reporting, milestone progress monitoring, and preparation of customer billing documentation.
• Offer cost control and planning guidance to the internal PMT team when needed.
• Perform and manage project activity scheduling and progress monitoring.
• Handle any other ad-hoc tasks assigned by management.
• Working effectively in an international environment, communicating fluently in Turkish is a plus but not a must. Fluency in English, both spoken and written required.

Vi söker en Projektingenjör till Trafikverket. 

Detta är ett konsultuppdrag. Stationeringsort är Göteborg.

Tjänsten är på heltid.

Uppdraget innebär ett nära samarbete med kunden vilket ställer stora krav på flexibilitet och samarbetsförmåga.

Uppdraget

Projektingenjör som biträder en eller flera projektledare inom anläggningsprojekt väg genom stöd i planering, administration och uppföljning av projekt avseende tid, kostnad, innehåll, risker, resurser, kvalitet, säkerhet, miljö och arbetsmiljö. Rollen innebär även interna och externa kontakter, deltagande i möten med konsulter och entreprenörer samt framtagning av underlag för uppföljning av entreprenörers leveranser.

Arbetsuppgifter

Biträda en eller flera projektledare

Stödja i planering, administration och uppföljning avseende tid, kostnad, innehåll, risker, resurser, kvalitet, säkerhet, miljö och arbetsmiljö

Bistå projektledaren i interna och externa kontakter

Medverka vid möten med konsulter och entreprenörer

Ta fram underlag för att följa upp leveransen från entreprenör

Bistå med förslag på beslut om åtgärder, handlingsalternativ och resursanvändning inom projektets ram

Medverka till att arbetet genomförs enligt lagar, regler, riktlinjer, förordningar och interna arbetssätt och processer

Överföra kunskap till Trafikverkets anställda avseende de arbetsuppgifter som utförs åt Trafikverket

Krav (OBS, obligatoriska)

Akademisk utbildning, teknisk inriktning, minst 120p inom ekonomi, teknik eller anläggning eller motsvarande kunskaper som beställaren bedömer som likvärdiga.

Minst 5 års erfarenhet, om minst 50% beläggningsgrad inom rollen, de senaste 5 åren av arbete inom anläggningsprojekt väg som projektingenjör, entreprenadingenjör, projektkoordinator eller projektekonom, varav 2 av de 5 åren ska ha varit sammanhängande i ett uppdrag.

Minst 5 års erfarenhet av riskhantering, tidsplanering och ekonomihantering i projekt.

Körkort för personbil.

Flytande svenska i tal och skrift. 

Meriterande 

Certifiering enligt TDOK 2018:0371 APV, minst enligt kraven i steg 2.2

Om oss

Centios övergripande mål är att vara ett konsultbolag som erbjuder smarta och hållbara lösningar som utvecklar samhället på ett positivt sätt.

Våra medarbetare erbjuds villkor som är anpassade för individen. Det innebär att arbetstider, arbetsomfattning, arbetsplats och kompetensutveckling så långt som möjligt anpassas utifrån medarbetarens behov.

Bland våra medarbetare hittar du engagerad personer som brinner för samhällsutveckling. Vi jobbar i små grupper där du kan bidra med dina erfarenheter samtidigt som du får ta del av andras kunskap och erfarenhet.

För oss är det viktigt med välmående och att hitta en sund balans mellan arbete och fritid. Därför har vi en nollvision mot stress och sätter trivsel och hälsa främst.

Läs gärna mer om oss på centio.se.

Vänligen skicka ditt CV på svenska. 

Vi ser fram emot din ansökan!

Beskrivning

Vi på Sustend Projektledning Öst söker en byggprojektledare som vill vara med och driva projekt för kommersiella fastighetsägare och offentliga organisationer. Vi arbetar nära våra kunder och tar ansvar från idé till färdigt resultat, alltid med fokus på kvalitet, tydlighet och hållbara lösningar.

Arbetsuppgifter

Som byggprojektledare hos oss leder du bygg- och renoveringsprojekt från start till mål. Du är navet mellan beställare, entreprenörer och myndigheter och ansvarar för att projekten levereras i tid, inom budget och enligt överenskommen kvalitet. Du kommer att:

• Planera, leda och följa upp byggprojekt
• Vara kundens representant genom hela processen
• Hantera budget, tidplan och kvalitetssäkring
• Koordinera alla inblandade aktörer

Kvalifikationer

• Har 3-5 års erfarenhet inom byggprojektledning eller motsvarande
• Har dokumenterad erfarenhet av projekt inom kommersiella fastigheter eller offentliga lokaler
• Är trygg i att driva projekt självständigt och ta ansvar för hela processen
• Har B-körkort
• Behärskar svenska i tal och skrift

Villkor

• Har stark entreprenörsanda
• Drivs av mål- och resultatfokus
• Har fokus på vår gemensamma tillväxtresa
• Besitter en social förmåga där kundnöjdhet, långsiktiga relationer och nätverkande faller sig naturligt.
• Uppskattar att arbeta i en organisation där vi gläds med och hjälper varandra i stort som smått.

Arbetsbeskrivning

Utbildning och Intyg

Erfarenhet

Lön och anställningsvillkor

Ansökan

Startdatum

Om oss

Job description

Profile

Application