Lediga jobb Magle Chemoswed AB i Malmö

Magle Group is growing and we are looking Regulatory Affairs Specialist who is looking for a new challenge and who wants to be part of a small but dynamic regulatory team. Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology. This role will focus on supporting our medical devices business and assure we comply with all regulatory standards and guidelines applicable in our active markets. The Regulatory Affairs Specialist plays a crucial role in the submission, registration, and lifecycle management of our medical device products.
Key Responsibilities:
Prepare and submit regulatory documentation required for the approval and registration of new and existing products in various international markets.
Be updated of regulatory procedures and changes in the regulatory climate to ensure compliance and advise the company on necessary adjustments.
Legalization of registration documentation.
Inform and educate the organisation on submission requirements and ensure necessary documents are provided.
Maintain regulatory files and update regulatory authorizations, such as Investigational Device Exemptions (IDEs), 510(k) submissions, Canadian medical device licenses, and CE dossiers for the EU, as well as NRTL certifications.
Maintenance of registrations , renewals, device listings, site registrations, supplements for changes, and annual reports.
Respond to questions from regulatory authorities.
Change control activities
Assess device-related incidents and complaints for medical device reporting requirements. Compile and submit reportable events to relevant regulatory authorities in a timely manner. Handle recalls and field actions, if required.
Review and create product labels and review promotional materials to ensure compliance with applicable regulations and technical standards.
Assist in preparing clinical trial site ethics review board applications for investigational device trials. Prepare interim or final reports for trial site ethics boards as required.
Other duties as assigned to support the regulatory team and ensure compliance with global regulatory requirements.

Qualifications:
Bachelor’s degree in a scientific or related field; advanced degree preferred.
Minimum of 5 years of experience in regulatory affairs, specifically with medical devices.
Strong understanding of international regulatory guidelines and standards such as FDA, CE Marking, NBOG, ISO 13485, MDR etc.
Proven track record in preparing successful regulatory submissions.
Excellent communication skills, both written and verbal, with the ability to interact effectively at all levels of the organization and with regulatory authorities.
Highly organized and able to manage multiple projects simultaneously in a fast-paced environment.

Meriting:
Experience with Class II and Class III medical devices.
Experience with APIs including CEP and ASMF files, is a plus.
Familiarity with regulatory landscape in key international markets (e.g., Europe, Asia, and North America).
Proficient with regulatory submission software and document management systems.


The position is located in Malmö on-site.

If you find the above position interesting, it fits your experience, and you want to join a company that has an interesting journey ahead, we would love to hear from you. We are a value driven organisation, and we expect you to share our passion to make an impact by making lives better for patients worldwide. Therefore we also look to find a person who not only fits the qualifications but also shares our values and fits our organisation personality wise.
In this process we will have a continuous recruitment. Please submit your CV and a short cover letter telling us why you find the position interesting. The position is placed at our office in Malmö and will be a full-time position. To find out more about us please visit our group web page: www.maglegroup.com Visa mindre

Är du en skicklig och erfaren ventilationstekniker som vill arbeta i en spännande och omväxlande roll? Vi söker en engagerad ventilationstekniker till vårt team som kan säkerställa optimal drift och underhåll av våra ventilationssystem.
Om oss
Magle Group är ett innovativt företag som arbetar med kontraktstillverkning av läkemedel, samt framställning egna produkter och medicinsk utrustning. Du kommer att vara en del av vår Engineering-avdelning och främst ansvara för uppgifter på vår anläggning i Malmö, men också i Lund samt Køge och Hårlev i Danmark. Engineering arbetar med hög kvalitet, effektivitet och kundnöjdhet som våra kärnvärden och vi söker nu en ny medarbetare för att stärka vårt team.

Dina primära ansvarsområden kommer att omfatta:
Installation, service och underhåll av ventilationssystem.
Felsökning och reparation av ventilationssystem.
Arbete med mekaniska, elektriska och datoriserade system.
Säkerställa att alla arbetsuppgifter utförs enligt gällande lagstiftning och säkerhetsnormer.
Dokumentation av utförda arbetsuppgifter.
Rådgivning i projekt om de bästa ventilationslösningarna.

Vi söker en kandidat med följande kvalifikationer:
Utbildning som ventilationstekniker eller motsvarande erfarenhet.
Erfarenhet av installation och service av ventilationssystem.
Kunskap om lagar och förordningar inom området.
Förmåga att arbeta självständigt och i team.
Körkort (B) är ett krav.
God teknisk förståelse och känsla för detaljer.

Vi erbjuder:
En spännande och utmanande tjänst med möjligheter till personlig och professionell utveckling.
En inspirerande och dynamisk arbetsmiljö i ett företag som prioriterar kvalitet och innovation.
En bra arbetsmiljö med erfarna och hjälpsamma kollegor.
Flexibel arbetstid och goda arbetsvillkor.

Vi är ett värderingsstyrt företag där våra principer bygger på IMPACT. Därför lägger vi stor vikt vid hur du passar in i vår verksamhet.
Låter denna tjänst som din nästa utmaning? Skicka in ditt CV och personliga brev till oss. Denna rekrytering kommer ske löpande så vi ser fram emot din ansökan snarast. Dock senast den 16 April, 2025.
Observera att du behöver ha ett gilitigt arbetstillstånd som möjliggör att du även kan arbeta i Danmark. Visa mindre

Magle Group är en ledande aktör inom life science och läkemedelstillverkning med produktionsanläggningar i Malmö och Lund (SE) samt Køge och Hårlev (DK). Vi söker nu en skicklig och engagerad processingenjör för att stärka vårt Engineering-team.
Vi erbjuder en dynamisk och innovativ arbetsmiljö där du får arbeta med både strategiska och operativa uppgifter. Du kommer att driva utvecklingen och optimeringen av våra produktionsprocesser, stödja den löpande driften och säkerställa att vi upprätthåller hög kvalitet och effektivitet enligt GMP-standard.
Som processingenjör kommer du att vara en viktig del av vårt Engineering-team och ansvara för att optimera och utveckla produktionsprocesser som uppfyller GMP-krav (Good Manufacturing Practice). Du är en naturlig lagspelare och trivs med att samarbetarbeta tvärfunktionellt för att nå gemensamma mål. Du är van att hålla många bollar i luften och är bra på att förklara och involvera dina stakeholders inom produktion, kvalitetssäkring och R&D, för att säkerställa att alla processer körs effektivt och håller GMP kvalitetsstandard. Vi ser att du kan arbeta strategiskt såväl som operativt.
Din arbetsplats kommer främst att vara i Malmö, men kommer även tills viss del innefatta Lund, samt Køge och Hårlev i Danmark.
Dina primära ansvarsområden kommer att omfatta:
Design, optimering och validering av produktionsprocesser i enlighet med GMP-standard.
Delta i utvecklingen av nya processer och tekniker, inklusive riskbedömning och processförbättring.
Utarbeta och uppdatera processdokumentation och SOP (Standard Operating Procedures).
Genomföra kvalificerings- och ändringsärenden samt hantera avvikelser.
Samarbete med kvalitetssäkring och EHS för att säkerställa efterlevnad av lagstiftning och GMP-standarder.
Felsökning och optimering av processer för ökad effektivitet och kostnadsbesparingar.
Delta i tvärvetenskapliga projektteam med fokus på att driva förbättringar.

Vi söker en kandidat med följande kvalifikationer:
Högeskoleexamen inom kemiteknik, bioteknik, tillverkning eller ett relaterat område.
Minst 3-5 års erfarenhet som processingenjör i en GMP-reglerad industri.
God förståelse för GMP, kvalitetshantering och kvalificering.
Erfarenhet av processförbättring, felsökning och optimering av produktionsprocesser
Goda kommunikationsfärdigheter, både muntligt och skriftligt, på svenska och engelska, kan du danska är det meriterande.
Förmåga att utföra systematisk problemlösning.
Förmåga att arbeta självständigt och ta ansvar för egna uppgifter.

Vi erbjuder:
En spännande och utmanande tjänst med möjligheter till personlig och professionell utveckling.
En inspirerande och dynamisk arbetsmiljö i ett företag som prioriterar kvalitet och innovation.
En bra arbetsmiljö med erfarna och hjälpsamma kollegor.
Goda karriärmöjligheter och en konkurrenskraftig lön.
Flexibel arbetstid och goda arbetsvillkor.


Vi är ett värderingsstyrt företag där våra principer bygger på IMPACT. Därför lägger vi stor vikt vid hur du passar in i vår verksamhet.
Låter denna tjänst som din nästa utmaning? Skicka in ditt CV och personliga brev till oss. Denna rekrytering kommer ske löpande så vi ser fram emot din ansökan snarast. Dock senast den 16 April, 2025.
Observera att du behöver ha ett gilitigt arbetstillstånd som möjliggör att du även kan arbeta i Danmark. Visa mindre

Magle Group is growing and we are looking for a Commercial Manufacturing Project Manager who is ready for a new challenge and who wants to be part of a small but dynamic project team.
Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology.
As a Commercial Manufacturing Project Manager, you will play a crucial role in ensuring the successful coordination and timely release of commercial production batches. Serving as the key link between multiple teams, you will oversee all critical activities, from production start-up through to final product release.
In this position, you will also provide critical support in Tech Transfer, ensuring smooth transitions from development to commercial manufacturing. A solid understanding of release processes, deviation investigations, and production coordination within regulated industries such as pharmaceuticals or medical devices is essential. Your ability to drive cross-functional collaboration, manage timelines, mitigate risks, and optimize resources will be key to ensuring the seamless execution of projects.
This newly created role offers you the opportunity to influence processes, enhance efficiencies, and contribute to the overall success of both production and commercial operations. If you excel in fast-paced environments, enjoy problem-solving, and are passionate about project management, this is an exciting opportunity to make a significant impact.
Key Responsibilities:
Collaborate with teams in QC, QA, Production, R&D, Supply Chain, and Engineering to ensure operational readiness.
Effectively manage project timelines, risks, and resources to achieve on-time and on-budget delivery.
Lead and coordinate commercial production projects, ensuring timely product release through effective cross-functional alignment.
Provide support in Tech Transfer, managing the smooth transition from development to production, ensuring operational continuity and compliance.
Ensure adherence to regulatory and quality standards, especially GMP and medical device regulations.
Serve as a liaison between internal teams and external stakeholders, facilitating clear communication and alignment.
Handle customer communication regarding deliveries for commercial batches, ensuring customers are informed of timelines, potential delays, and any changes.
Drive and optimize processes for batch coordination, release, and product quality improvement.
Generate and maintain comprehensive project documentation, including status reports, timelines, and compliance records.
Take on additional commercial production projects as needed to support business objectives and enhance operational efficiency.
Perform other duties as assigned to support the project management team.


Qualifications:
Bachelor’s degree in a scientific or related field; advanced degree or relevant industry experience preferred.



What we are looking for:
Proven project leadership experience in regulated industries such as pharmaceuticals, biotech, medical devices, or related fields.
Strong background in operational QA, production engineering, or similar roles within the medical device or pharmaceutical industry, with additional experience in supply chain, manufacturing, or production coordination considered a plus.
Extensive knowledge of medical device regulations, GMP, quality systems, release processes, deviation management, and production workflows.
Experience working with customers or acting as a liaison to ensure clear communication and alignment on project goals and deliverables.
Demonstrated ability to manage multiple stakeholders and work cross-functionally.
Strong organizational, leadership, and project management skills.
Excellent communication and problem-solving abilities.
Proven track record of delivering impactful results


If this position aligns with your experience and you’re excited about joining a company with a promising future, we’d love to hear from you.
We are a value-driven organization, and we seek individuals who share our passion for making a meaningful impact and improving lives. We’re looking for someone who not only meets the qualifications but also embraces our values and fits within our organizational culture.
This is an ongoing recruitment process. Please submit your CV along with a brief cover letter explaining why you’re interested in this position. The role is based at our office in Malmö, with collaboration at our sites in Lund and Denmark. It’s a full-time position. Visa mindre

We are seeking a highly motivated and detail-oriented Financial Accountant/Controller to join our headquarters in Malmö. In this key position, you will support our growing operations in Sweden, Denmark, and Germany, contributing directly to the company’s success through hands-on financial management and strategic oversight. If you are proactive, results-driven, and ready to take ownership of financial processes, we invite you to join our ambitious team.
The Role:
As a Financial Accountant/Controller, you will actively drive and develop financial processes, and be part of the finance team that supports the business in Sweden, Denmark and Germany. You will work close to the business and have several internal as well as external stakeholders. This role demands a solutions-oriented approach, where you will work to align financial strategies across all parts of the organisation.
You will have an instrumental role in providing financial oversight, and you will be responsible for the end-to-end bookkeeping of one of our subsidiaries, which includes the monthly, quarterly and annual closing.
Key Responsibilities:
Hands-on financial and management accounting.
Control and analysis of costing and budgets
Cash flow management and forecasting
First point of contact for our external auditors regarding questions
Perform month-end, quarterly and annual closings.
Ensure compliance with local accounting standards (GAAP)
Manage salary administration, travel expenses, and liaise with the tax agency.
Oversee VAT, tax, and social security reporting, maintaining full accuracy.
Drive financial improvements, reviewing current routines and identifying efficiencies.
Prepare and present financial reports, offering strategic insights to senior management.
Support the Annual Report process in line with regulatory requirements.
Take ownership for ad-hoc financial projects, providing tailored solutions for internal and client needs.

About You:
To thrive in this role, you’ll need to be self-driven, with a sharp eye for detail and a passion for getting things done. This is a dynamic, hands-on position that requires a high level of ownership, proactive problem-solving, and the ability to pivot as business needs evolve.
Solid background in financial accounting and controlling.
Strong organizational skills and the ability to manage competing priorities in a matrix style organization.
Strong experience with bookkeeping, salary administration, taxes, VAT, and expenses.
Familiarity with Swedish GAAP (knowledge of Danish GAAP and IFRS is an asset).
Skilled in using financial software and tools, with the ability to analyze and present data.
Experience working in multi-entity environments, particularly across international subsidiaries, is a plus.
Fluent in English (written and spoken), with clear and concise communication skills. Proficiency in Swedish and Danish is beneficial, although not essential.

About Us:
We provide a workplace where autonomy, initiative, and a roll-up-your-sleeves attitude are highly valued. With a flat organizational structure, you will be able to influence and be part of improving our ways of working and contribute to the future success of the company.
If you’re looking for a role where you can make an impact from day one and grow alongside a highly skilled team, we look forward to receiving your application.
The Recruitment Process:
The last day to apply for this positionis the 16th of February.We apply a rolling selection. We place great importance on how well your personality will fit the company, and how you can make an IMPACT, when selecting candidates. Visa mindre

Magle Chemoswed är ett innovativt farmaceutiskt och medicintekniskt företag i Malmö. Vår expertis ligger inom utveckling och tillverkning av aktiva läkemedelssubstanser (API) såväl som formulering av system för läkemedelsdistribution i kroppen. Vi arbetar innovativt för att lyckas förverkliga idéer till att bli produkter som kan hjälpa patienter få ett bättre liv.
Vi söker dig som vill arbeta extra under dina studier och som har ett intresse av läkemedels- eller livsmedelsproduktion och alla delar av olika tillverkningsprocesser. Den huvudsakliga uppgiften kommer vara att bistå den manuella och automatiserade etiketteringen. samt packningav våra produkter. Dessa processer sker i en manuell/semiautmatisk process och det finns goda möjligheter att lära sig andra steg inom produktionen. Som läkemedelsbolag arbetar vi enligt GMP (Good Manufacturing Practice)med höga kvalitetskrav och arbete enligt överenskomna processer. Då kvalitet är ett fundament för allt arbete som sker inom vår branch så kommer vi även kunna erbjuda extra arbete för dig som är intresserad av att lära dig vissa analyser och tekniker inom QC (Quality Control).
Vi arbetar med farmaceutiska samt medicintekniska produkter enligt GMP och ISO13485 standard vilket innebär att du kommer få ta del av en rad utbildningar inom dessa kvalitetssystem. Övriga utbildnngar kommer vara relaterade till de arbetsuppgifter som du utför men kan vara kring renrumsarbete, analysmetoder, processkemi etc.

Vi söker dig som:
Har fyllt 18 år
Har en teknisk förståelse och gillar att blanda teori med praktiskt arbete
Går en ingenjörsutbildning eller annan naturveteskaplig utbildning
Är bra på att arbeta noggrant och följa instruktioner
Har god förmåga till dokumentation.
Tar ansvar för dina arbetsuppgifter och säkerställer att inget tappas mellan stolarna.
Har ett intresse av att arbeta enligt kvalitetssystem och noga beskrivna rutiner.
Har ett intresse av att föreslå samt utföra förbättringar av skrivna rutiner.
Talar och skriver svenska och engelska
Vi är ett företag som har en stark företagskultur där vi förstår att hur vi agerar och utför vårt arbete gör en skillnad för våra slutkunder som är patienter. Vi tar ansvar för varandra och för vår verksamhet och för att trivas hos oss måste du dela våra värdegrunder.
Tjänsten är på deltid. Du förväntas kunna arbeta minst 4 helgdagar i månaden. Det kommer utöver helgarbete finnas möjlighet till pass under kväll- & dagtid under vardagar. Det kommer även finnas behov vid arbete under lov och storhelger.

Vi lägger stort vikt vid personlighet och att du är en person som pålitlig, nyfiken och intresserad av att lära dig nya saker samtidigt som du vill vara del i ett team som har som främsta mål att få ut produkter som hjälper patienter till ett bättre liv. Visa mindre

We are seeking a highly motivated and detail-oriented Financial Accountant to join our headquarters in Malmö. In this key position, you will support our growing operations in Sweden, Denmark, and Germany, contributing directly to the company’s success through hands-on financial management and strategic oversight. If you are proactive, results-driven, and ready to take ownership of financial processes, we invite you to join our ambitious team.
The Role:
As a Financial Accountant, you will actively drive and develop financial processes, and be part of the finance team that supports the business in Sweden, Denmark, and Germany. You will work close to the business and have several internal as well as external stakeholders. This role demands a solutions-oriented approach, where you will work to align financial strategies with across all parts of the organisation.
You will have an instrumental role in ensuring financial accuracy, you will be responsible for bookkeeping as well as being part of monthly closing and present monthly and quarterly reports.
Key Responsibilities:
Hands-on financial management of accounts, ensuring accuracy and efficiency.
Control and analysis of group financial data.
Cash flow management
Perform month-end and quarterly closings.
Ensure compliance with local accounting standards (GAAP)
Manage salary administration, travel expenses, and liaise with the tax agency.
Oversee VAT, tax, and social security reporting, maintaining full accuracy.
Drive financial improvements, reviewing current routines and identifying efficiencies.
Support the Annual Report process in line with regulatory requirements.
Spearhead special financial projects, providing tailored solutions for internal and client needs.

About You:
To thrive in this role, you’ll need to be self-driven, with a sharp eye for detail and a passion for getting things done right the first time. This is a dynamic, hands-on position that requires a high level of ownership, proactive problem-solving, and the ability to pivot as business needs evolve.
Solid background in financial accounting, or a related field.
Strong organizational skills and the ability to manage competing priorities.
Proven experience with bookkeeping, salary administration, taxes, VAT, and expenses.
Familiarity with Swedish GAAP (knowledge of Danish GAAP and IFRS is an asset).
Skilled in using financial software and tools, with the ability to analyse and present data.
Experience working in multi-entity environments, particularly across international subsidiaries, is a plus.
Fluent in English (written and spoken), with clear and concise communication skills. Proficiency in Swedish and Danish is beneficial, though not essential.

About Us:
We provide a workplace where autonomy, initiative, and a roll-up-your-sleeves attitude are highly valued. With a flat organizational structure, you will be able to influence and be part of improving our ways of working and contribute to the future success of the company.
If you find the above position interesting, it fits your experience, and you want to join a company who has interesting journey ahead we would love to hear from you. We are a value driven organisation, and we expect you to share our passion to make an impact by making life better, therefore we also look to find a person who not only fits the qualifications but also shares our values and fits our organisation personality wise.
In this process we will have a continuous recruitment, please submit your CV and a short cover letter telling us why you find the position interesting asap but at latest the 10th of November.The position is placed at our office in Malmö. To find out more about us please visit our group web page. www.maglegroup.com Visa mindre

Magle is growing and we looking for an ambitiousBusiness Development Manager that can strengthen ourBusiness Development team. We are looking for you who have experience fromCDMO activities, pharmaceuticals, and medical devices, and who us keen on identifying new business opportunities, managing client relationships, and contributing to our growth strategy.
Key Responsibilities:
Identify and develop new business opportunities in the pharmaceutical and medical device sectors, with a focus on expanding our CDMO services.
Stakeholder management - maintain and strengthen relationships with existing clients, understanding their needs and providing tailored solutions that enhance client satisfaction and retention.
Analyze market trends and competitive landscape to develop strategic plans for entering new markets or expanding in existing ones.
Collaborate with cross-functional teams, including R&D, Regulatory Affairs, and Marketing, to develop compelling proposals and presentations for potential clients.
Participate in industry conferences and networking events to represent Magle Group and identify potential business leads.
Manage the end-to-end sales process from initial contact through contract negotiation and closure, ensuring alignment with the company’s strategic objectives and compliance standards.
Prepare regular reports on sales activities, pipeline, and forecasts for senior management.
Support the development and execution of strategic partnership agreements and alliances.
Provide feedback from the market to the product development and operations teams to help shape future strategies and innovations.

Qualifications:
Bachelor’s degree in Business Administration, Marketing, Life Sciences, or a related field; an MBA is a plus.
Minimum of 3 years of experience in business development, preferably within the pharmaceutical, CDMO, or medical device sectors.
Demonstrated track record of successful sales and client management.
Strong understanding of the pharmaceutical and medical device industries, including regulatory and market trends.
Excellent communication, negotiation, and interpersonal skills, with the ability to engage and influence stakeholders at all levels.
Proven ability to work effectively in a dynamic, team-oriented environment.
Willingness to travel as needed to meet business objectives.
Strong communication skills
Fluent in English both written and oral - additional language such as any Nordic language,French, German and Spanish considered a plus

If you find the above position interesting, it is in line with profileand you want to join a company who has interesting journey ahead , we would love to hear from you. We are a value driven organization and we expect you to share our passion to make an impact by making life better, therefore we also look to find a person who not only fit the qualifications but also shares our values and fit our organisation personal wise.
In this process we will have an continuous recruitment, please submit your CV and a short cover letter telling us why you find the position interesting. The position is placed at our office in Malmö and will be a full time position. To find out more about us please visit our group webb page. www.maglegroup.com Visa mindre

Are you an experienced QA Specialist that have a passion for quality? Do you love to work cross-over with other department and develop processes and find better, more efficient ways to work?

Join us at Magle Chemoswed! You will play a key role in securing quality and thus enable us to bring life changing healthcare innovations to patients. We are an ambitions company that strive towards new ways of working in order to develop and improve to help patients in need. Having high quality products is key for our success.

To succeed in the role of QA Specialist at Magle, you should enjoy working both independently and with others - strong collaboration and communication skills are crucial for this position. You should also feel comfortable in a changing environment and be able to adjust your work depending on the business needs. We look for someone who is organized, driven, efficient, and capable to explain and support the organization in quality matters.

Key Responsibilities:

- Responsible for reviewing batch documentation.

- Release APIs, raw materials, and deliveries.

- QA approval of Standard Operating Procedures (SOPs).

- Manage changes, deviations, and complaints.

- Provide customer support.

- Participate in customer and regulatory inspections, investigations, and risk assessments.

- QA encompasses a broad range of tasks, and there are opportunities for development in various areas.

Requirements for the Position:




- University degree in chemistry, pharmaceuticals, or equivalent engineering discipline.

- Previous work experience in pharmaceutical or Medical Device operations according to GMP and ISO 13485

- Excellent proficiency in both Swedish and English, spoken and written, as both languages are used in the job.

- Experienced user of Microsoft Office and a Q Management system

- Experience in QA work for projects in clinical phases is highly advantageous.

If you are passionate about making a meaningful impact and feel the above position fits your experience, we would love to hear from you. In this process we will have an continuous recruitment, please submit your CV and a short cover letter telling us why you find the position interesting. The position is placed at our office in Malmö and will be a full time position. To find out more about us please visit our group Webb page. www.maglegroup.com Visa mindre

Magle Group is a dynamic company within in the pharma industry. We are a team of 80 dedicated professionals with different areas of expertise, we have the total value chain from early development to large scale manufacturing. Working at Magle means you make an impact for others, we are culture driven company, always aware that our work improves the living conditions for patients around the world. To learn more about us visit: https://maglegroup.teamtailor.com/

We are looking for you who wants to take a first step towards working as a legal counsel and who is interested in working close to business. We look for a highly motivated person that naturally takes ownership and is at the end of your studies or in the beginning of your career and are eager to explore how it is to work as a legal counsel within a company where you will support a diverse range of legal matters and gain valuable experience in company environment. The position is a vacancy position that will last until April 2025 since our legal counsel will be on parental leave.

Position Overview:

As a Junior Legal Counsel at Magle, you will play a key role in supporting the organization in legal matters. This position offers a unique blend of responsibilities, allowing you to gain exposure to various aspects of legal practice within a business setting. You will be preparing legal documents, maintaining filings, liaising with authorities, taking charge of the secretarial work for the Board. creating presentations for board meetings and providing valuable legal advice to support our business operations.

Key Responsibilities:

Legal Document Preparation: Draft, review, and finalize legal documents, ensuring accuracy and compliance with relevant laws and regulations.

Filing and Compliance: Manage and maintain organized legal files, ensuring the company's compliance with all applicable laws and regulations, including rules applicable to the listing environment.

Government Authorities Liaison: Establish and maintain effective communication with relevant government authorities, ensuring timely and accurate submissions.

Board Meeting Support: Prepare and present legal documents and presentations for board meetings, collaborating with other departments to provide comprehensive insights.

Business Advisory: Provide legal support and advice to different business units, helping navigate legal issues and contributing to informed decision-making.

Agreement Management: Review, draft, and negotiate agreements with partners, both customers and suppliers, ensuring the company's interests are protected.

Legal Research: Stay updated on legal changes and developments that may impact the company, and communicate relevant information to the team.

Qualifications:

Jur kand (LLM) degree or equivalent degree within the field of law/business law

Strong organizational and multitasking skills.

Excellent communication and interpersonal abilities.

Detail-oriented with a commitment to producing high-quality work.

Professional knowledge of English and Swedish

Notary service or other experience from administrative work

In this position you need to be able to structure your work and be able to prioritize. We need you to be organized and thorough and able finding information that can help you to give answers. We are in a fast-moving environment and there is a need that you are flexible and can adjust your work when needed. In this position you will work close to our CEO and the executive team at Magle and you need to be able to handle confidential information and have a high integrity. We will in this recruitment process place great emphasis on personal qualities.

If you find the above position interesting, we want to get to know you. Please send us your CV and a short personal letter why you think this position would be a match for your aspirations. We will have a continuous recruitment process so please apply as soon as possible but no later than April 4th. Visa mindre

For our HQ in Malmö, we are now looking for an efficient, creative, and detail-oriented Financial Accountant/Controller who will support our entities in Sweden and Germany. We invite you to join our dynamic team for an exciting journey and be a part of our future success!
About the role:
In this role, you will support and develop the financial process and routines, and work together with the finance team in Sweden to serve the organization and our external partners. You will work in close corporation with both the local team and our German team and in the long-term perspective be responsible for implementing the aligned strategy for Finance. You will together with Management ensure that the financial performance of the subsidiary meets the Company budget, expectations, and targets. You will be responsible for trend mapping and analysis of the performance and requirements etc. Alongside the Financial Accountant, our long-term ambitions are that you will be our Financial Controller, making sure that we have correct information and data for our monthly and quarterly reports.
Today, you may be working as a Financial Accountant, hoping to move toward a position that includes responsibilities as a Controller.


Key tasks (among others):
Manage day-to-day company accounts
Oversee budget forecasting and cashflow management
Controlling of Group financial data
Responsible for local accounting in subsidiary
Salary support and travel expenses handling
Participate in monthly closing routines set by the head office
Support with Annual Report accordingly to local GAAP
Support monthly financial closings/statements with inventory and scanning of goods and materials
Primary contact for Tax agency
Monthly reconciliation of accounts
Reconciliation of bank accounts
Monthly VAT, tax, and social security contribution reporting
Be involved in reviewing routines and activities in finance and suggest and implement improvements
Assign and follow up any special projects to be performed for a customer or project
Provide comprehensive financial updates to senior managers by evaluating, analysing, and reporting appropriate data points



We encourage you to apply even if you feel that you don’t have experience in everything that is listed above.
Who do we think you are to succeed in this role?
Fluent in English, both verbal and written
Education in financial accounting, finance controlling, or equal
Good IT skills
Credible and confident communicator (written and verbal) at all levels
First-class planning, organizational, and time management skills
Experienced in working with bookkeeping, salaries, taxes, VAT, and travel expenses
Experience and interest in finance controlling
Knowledge of Swedish GAAP. It is an advantage if you also have knowledge of German GAAP and IFRS
Communicating in German and Swedish would also be beneficial



What’s in it for you?
As an employee, we are committed to providing you with a wide range of real-world experiences and responsibilities that will accelerate your learning curve and give you tools for future success. You will have the opportunity to learn, explore, and gain hands-on experience within the area and make a real impact on the company. Also, you will have an exceptional opportunity to influence the team’s future success through your ideas and contributions and be part of a very enthusiastic and open-minded team with highly skilled colleagues. There will be a lot of growth potential for this role.
If you’re passionate about being a part of a flat networked organization that works to find innovative solutions to health care challenges and want to be a part of a tightly knit team, we look forward to your application.
About us:
Magle Chemoswed is a contract development and manufacturing organization with a strong track record of bringing new products to the market for its customers in the global pharmaceutical and medical device industry. The company provides CDMO services ranging from product development to full scale commercial manufacturing. By owning its manufacturing and development facilities, the company has all the resources required to successfully manage CDMO work in the pharmaceutical and medical device fields.


Other information:
Start date: as soon as possible
Location: Malmö
Fulltime position



Applications should be sent to [email protected]. We will review applications on an ongoing basis. We look forward to speaking to you soon. For questions, please contact Nellie Månsson, the People Experience Associate at [email protected] Visa mindre

For the QC/Analytical Development Department located in Malmö, we currently have an exciting opening for an experienced Analytical Chemist.


About us:
Magle Chemoswed is a contract development and manufacturing organization with a strong track record of bringing new products to the market for its customers in the global pharmaceutical and medical device industry. The company provides CDMO services ranging from product development to full scale commercial manufacturing. By owning its manufacturing and development facilities, the company has all the resources required to successfully manage CDMO work in the pharmaceutical and medical device fields.


In this role, you will be part of the Quality Control team and playing an active role in the growth strategy of the company. You will be part of the team responsible for supporting the Contract Development and Manufacturing Organisation. You will be responsible for testing and releasing raw materials, intermediates and finished products to strict timescales, in order to support the business requirements.


Key tasks (among others):
Testing of raw materials, intermediates and finished products using current pharmacopoeias, any associated ‘wet’ chemistry and instrumental techniques (HPLC, GC, IR, UV, IC, ICP and titration) as appropriate.
Preparing Quality reports, including analytical reports (for raw materials and finished products) and stability reports.
Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.
Stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, UV) techniques, as appropriate.
Writing analytical specifications using current pharmacopoeias and reviewing existing analytical specifications.
Writing/reviewing Standard Operating Procedures (SOPs).
Calibrating analytical equipment, as and when required.
Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
Observing and complying with ISO13485, Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
Observing and complying with company Health and Safety Policies and SOPs.



Who are you?
Fluent in Swedish and English
Degree or education in a scientific discipline (with strong chemistry content).
Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
Highly proficient in the use of key analytical equipment (HPLC, IR, UV, GC, Titration etc) and the testing of finished products.
Experience of working in a GMP environment.
Good IT skills
Credible and confident communicator (written and verbal) at all levels.
Customer focused and passionate about delivering excellent customer service.
Ability to achieve and maintain high standards with meticulous attention to detail.
First class planning, organisational and time management skills.
A team player with the ability to work accurately in a busy and demanding environment, adhering to strict deadlines/timescales.



Why should you apply?


You will have an exceptional opportunity to influence the future success of the team through your ideas and contributions and be part of a very enthusiastic and open-minded team with highly skilled colleagues.
If you’re passionate about being a part of a flat networked organisation that works to find innovative solutions to health care challenges and want to be a part of a tightly knit team, we look forward to your application.
Other information:
Start date: as soon as possible
Location: Malmö
Full-time position



Applications should be sent to [email protected]. We look forward to speaking to you soon. For questions, please contact Nellie Månsson, People Experience Associate at the email above. Visa mindre