Careers

Job Title: Senior Manager, Global Regulatory
Location: Solna, Stockholm, Sweden 
Employment Type: Permanent, 100%

About Immedica

Immedica is a pharmaceutical company, headquartered in Stockholm, Sweden, focused on the commercialization of medicines for rare diseases within metabolic, neurology, hematology & oncology, endocrinology and specialty care. Immedica’s capabilities cover marketing and sales, compliance, pharmacovigilance, quality assurance, external manufacturing, regulatory and medical affairs as well as market access. Serving patients in more than 50 countries, Immedica is fully dedicated to helping those living with diseases which have a large unmet medical need.

Immedica was founded in 2018 by investment company Impilo and buy-in management and currently employs more than 180 people across Europe, the Middle East and the US. Of these, approximately 80 are based in the headquarters in Life City, Hagastaden, Stockholm.

At Immedica, our core values are the foundation of our culture and the driving force behind how we operate, innovate, and collaborate. These values guide every decision we make, shaping our commitment to patients, partners, and colleagues.

Immedica's regulatory affairs department currently consists of sixteen people and we are now searching for an additional team member to join us as CMC regulatory expert.

This is a perfect opportunity for you who want to grow and develop within regulatory affairs CMC at an expansive Swedish company in a true global environment. 
In this position, the primary task would be to provide regulatory strategy and guidance for assigned products and projects with focus on CMC. This includes leading, preparing and reviewing CMC regulatory submissions across global markets.

You will be part of the HQ Global regulatory department and work closely with other HQ functions of the company, such as QA, Manufacturing, Supply and Commercial to secure the quality and supply of the Immedica products. 
 

Job description and responsibilities

The role include:

• Act as CMC regulatory expert for assigned products and lead regulatory CMC submissions in a global setting, including new market registrations and post-approval submissions
• Prepare, review, and coordinate high-quality CMC documentation to ensure compliance with global regulatory requirements and internal standards
• Collaborate closely with internal product teams and external manufacturing & laboratory partners (CMO/CLO) to ensure regulatory compliance, quality and adherence to timelines
• Participate in cross-functional internal projects as a regulatory expert for assigned products
• Track global CMC regulations and guidelines and share relevant updates and best practices across the regulatory organization
• Participate in updates and implementations of relevant SOPs

Experience and competence

We are looking for someone with a university degree in pharmacy/chemistry/biotechnology or equivalent, preferably with several years of experience from working in the pharmaceutical industry with a focus on regulatory CMC and biological medicinal products. Experience in leading major, global pre- and post‑approval CMC submissions (e.g., new marketing authorization applications and manufacturing tech transfers) and CMC regulatory interaction with EMA, FDA, ANVISA, COFEPRIS and PMDA is meriting. 
Excellent knowledge of English, both spoken and written, is a requirement. Knowledge of Swedish language is preferred.

Personal qualities

As a person, you are independent, ambitious, clear and meticulous. You have good teamwork skills and like to tackle new things. The ability to structure, obtain information and investigate information that is new to you is valued.

We welcome applicants from all backgrounds, and we encourage you to apply even if you feel you do not match 100% of the technical requirements. We celebrate diversity, promote inclusivity, place great emphasis on personal qualities and alignment with the company’s core values.

How to apply

Please send your application or any questions about this position to [email protected]. 
Applications are reviewed on a rolling basis, so we encourage you to apply as soon as possible.
 

We look forward to welcoming you to the Immedica team!

Are you interested in working with Patient Safety for Rare diseases in a growing global company?

Job Title: Drug Safety Associate
Location: Stockholm, Sweden
Employment Type: Full Time

Immedica Pharma has experienced remarkable growth in recent years, and we are now looking for a Drug Safety Associate to further strengthen our Global Drug Safety department.

At Immedica, patient safety is at the core of everything we do. The Drug Safety function plays a critical role in ensuring that our products are monitored, evaluated, and managed in line with global pharmacovigilance requirements, contributing directly to patient wellbeing and regulatory compliance.

This is an excellent opportunity to develop within pharmacovigilance in a dynamic, entrepreneurial, and fast-growing Swedish company headquartered in central Stockholm (Torsplan). You will report to Head of Global Drug Safety, Arvid Cronlund, and be part of a collaborative and growing Global Drug Safety team at Immedica.

Job description and responsibilities

The Drug Safety Associate role includes

• Working with case processing, including data entry, coding, and quality control of adverse event reports
• Performing related pharmacovigilance activities such as reconciliation, literature screening, and basic data/statistics handling
• Collaborating regularly with internal functions such as Regulatory Affairs, Quality Assurance, Medical Information, and affiliates
• Working closely with external partner companies globally 

As the company grows, there will be opportunities to develop in the role. This may include contributing to process and routine development, supporting training activities, and taking on increased responsibility for the company’s safety database.

Experience and competence

To fit in this role, you should have a BSc or MSc in Pharmaceutical sciences, Biomedicine or similar. Experience from pharmacovigilance related work in the pharmaceutical industry is a merit. You are fluent in Swedish and English both speaking and writing. 
You are structured and detail-oriented in your way of working. To thrive in this role, you are motivated by working in an environment characterized by entrepreneurship and drive. At Immedica, we take a high degree of individual responsibility for our work, while collaboration is essential to overcome challenges along the way.
We are a small team that values a positive work environment and enjoys working together. Are you ready to grow and develop together with Immedica?

How to apply

This is a full-time position based at our office at Torsplan in Stockholm. Please send your application to [email protected], with the Subject “Drug Safety Associate”. Please send your application no later than May 3rd, 2026. Please note, applications are reviewed on an ongoing basis, so we do encourage you to apply as soon as possible.

About Immedica

Immedica is pharmaceutical company, headquartered in Stockholm, Sweden, focused on the commercialization of medicines for rare diseases within metabolic, neurology, hematology & oncology and specialty care. Immedica’s capabilities cover marketing and sales, compliance, pharmacovigilance, quality assurance, regulatory and medical affairs as well as market access. Serving patients in more than 50 countries, Immedica is fully dedicated to helping those living with diseases which have a large unmet medical need.
Immedica was founded in 2018 by investment company Impilo and buy-in management and currently employs around 180 people across Europe, the Middle East and the US.  Of these, approximately 80 are based in the headquarters in Life City, Hagastaden, Stockholm.

At Immedica, our core values are the foundation of our culture and the driving force behind how we operate, innovate, and collaborate. These values guide every decision we make, shaping our commitment to patients, partners, and colleagues.

Open & Honest: We foster transparency, integrity, and trust through open communication. 
Effective: Focused on delivering excellence, we prioritize impact and quality to make a real difference in the rare disease landscape.

Empowered: We encourage collaboration and ownership, creating a supportive workplace where all team members’ contributions drive innovation and growth.

We look forward to welcoming you to the Immedica team!

Are you our next KAM in Northern Italy?

Job Title: Key Account Manager Endocrinology Rare Disease North/Central Italy
Location: Italy, North / Central
Employment Type: Full time

Immedica Pharma has experienced remarkable growth in recent years, and we are now looking for a KAM to further strengthen our Italian team in the north region.  

Immedica has adapted quickly to become an increasingly sophisticated rare disease and niche products pharmaceutical company and strive to be well known for its outstanding launch capabilities & commercial operations. Immedica is continuing to grow and with this exciting position also take the next step in the therapeutic area of endocrinology rare diseases in Italy.

We are looking now for an experienced Key Account Manager accountable to operate at multiregional  level primarily in center-north of Italy, in this position the Key Account Manager will be mainly responsible for building and maintaining strong relationships with key accounts and support the region to increase sales and profitability, implementing strategic market access activities for current and future assets.

As a Key Account Manager, you should be organized and able to analyze performance metrics. We also expect you to have the ability to deploy strategic accounts plan and to foster relationships with customers identifying  valuable projects to effectively address the needs of targeted audiences.

As Key Account Manager you will be a key driver and contributor in the local cross-functional team, but also an important player in all collaboration with the Immedica Global Team, the Medical colleagues as well as colleagues across country borders, to share knowledge, learnings and best-practices insights.

The Key Account Manager for Endocrinology rare diseases also support pre-launch activities for Immedicas new products and supports a significant scientific exchange. 

The position is a field position based in Italy, reportin directly to General Manager Italy & Greece.

Job description and responsibilities

The KAM Endocrinology Rare Disease role includes
•    Bring up a positive image of the company providing valuable scientific knowledge on products and disease awareness  
•    Set and monitor sales targets and other relevant KPIs for the region and collect and analyze sales data and trends. Ensure all activities are in line with set cost.
•    Network with key customers to identify and address specific needs
•    Develop and maintain relationships with customers to ensure Immedica is adapting to market needs and requests
•    Act as the liaison between customers and internal teams ensuring clients’ requirements are met
•    Identify and attract prospective strategic customers
•    Ensure brand consistency, e g through the Country Implementation Plan, contribute to defined brand strategy and the development of promotional tools or other relevant documentation. 
•    Collect and compile competitive intelligence in a structured way, and ensure shared internally.
•    Liaise cross-functionally to set and implement strategies for new products
•    Stay up-to-date with internal and external developments and suggest new ways to increase sales. Keep a high scientific level in the area of Endocrinology and proactively participate or build up occasion of important scientific exchange (e.g. Congresses, education/training session) 
•     Knowledge of local market access dynamics and able to implement valuable projects for  products time to the market optimization 
•    Actively advocate Immedica values and conduct all activities to highest ethical standards in accordance with country code of practice and local Laws and regulations.

Experience and competence

•    Proven work experience in Key Account Management
•    Structured collection of customer insights and competitive analysis 
•    Pursuit for sales force excellence ensuring optimal targeting and segmentation of the market.
•    Solid experience in sales and project management 
•    Demonstrable experience in negotiating and meeting clients requirements
•    In-depth understanding of sales performance metrics and the analytical skills to take relevant actions
•    Hands on experience with CRM software and MS Excel
•    Availability to travel is needed

A Scientific university degree (PhD/PharmD) is required, as well as fluency in English.  

To have obtained the expected experience and skills, we believe you have a minimum of 5 years of relevant work experience within the pharmaceutical industry. 

In addition, you have excellent analytical and organizational skills, strong communication skills and is flexible and adaptable to fit in to our growing organization.

How to apply

This is a full-time position based at our Italian affiliate. Please send in your application in English to [email protected] with the Subject line “KAM Endocrinology North / Central Italy”. Applications are reviewed on an ongoing basis, so we encourage you to apply as soon as possible.

About Immedica

Immedica is pharmaceutical company, headquartered in Stockholm, Sweden, focused on the commercialization of medicines for rare diseases within metabolic, neurology, hematology & oncology and specialty care. Immedica’s capabilities cover marketing and sales, compliance, pharmacovigilance, quality assurance, regulatory and medical affairs as well as market access. Serving patients in more than 50 countries, Immedica is fully dedicated to helping those living with diseases which have a large unmet medical need.
Immedica was founded in 2018 by investment company Impilo and buy-in management and currently employs around 180 across Europe, the Middle East and the US.  Of these, approximately 80 are based in the headquarters in Stockholm. 
At Immedica, our core values are the foundation of our culture and the driving force behind how we operate, innovate, and collaborate. These values guide every decision we make, shaping our commitment to patients, partners, and colleagues. Open & Honest: We foster transparency, integrity, and trust through open communication. Effective: Focused on delivering excellence, we prioritize impact and quality to make a real difference in the rare disease landscape. Empowered: We encourage collaboration and ownership, creating a supportive workplace where all team members’ contributions drive innovation and growth. 

We look forward to welcoming you to the Immedica team!

Are you our next KAM in Southern Italy?

Job Title: Key Account Manager Endocrinology Rare Disease South/Central Italy
Location: Italy, South / Central
Employment Type: Full time

Immedica Pharma has experienced remarkable growth in recent years, and we are now looking for a KAM to further strengthen our Italian team in the south / central region.  

Immedica has adapted quickly to become an increasingly sophisticated rare disease and niche products pharmaceutical company and strive to be well known for its outstanding launch capabilities & commercial operations. Immedica is continuing to grow and with this exciting position also take the next step in the therapeutic area of endocrinology rare diseases in Italy.

We are looking now for an experienced Key Account Manager accountable to operate at multiregional  level primarily in center-south of Italy, in this position the Key Account Manager will be mainly responsible for building and maintaining strong relationships with key accounts and support the region to increase sales and profitability, implementing strategic market access activities for current and future assets.

As a Key Account Manager, you should be organized and able to analyze performance metrics. We also expect you to have the ability to deploy strategic accounts plan and to foster relationships with customers identifying  valuable projects to effectively address the needs of targeted audiences.

As Key Account Manager you will be a key driver and contributor in the local cross-functional team, but also an important player in all collaboration with the Immedica Global Team, the Medical colleagues as well as colleagues across country borders, to share knowledge, learnings and best-practices insights.

The Key Account Manager for Endocrinology rare diseases also support pre-launch activities for Immedicas new products and supports a significant scientific exchange. 

The position is a field position based in Italy, reporting directly to General Manager Italy & Greece
 

Job description and responsibilities

The KAM Endocrinology Rare Disease role includes
•    Bring up a positive image of the company providing valuable scientific knowledge on products and disease awareness  
•    Set and monitor sales targets and other relevant KPIs for the region and collect and analyze sales data and trends. Ensure all activities are in line with set cost.
•    Network with key customers to identify and address specific needs
•    Develop and maintain relationships with customers to ensure Immedica is adapting to market needs and requests
•    Act as the liaison between customers and internal teams ensuring clients’ requirements are met
•    Identify and attract prospective strategic customers
•    Ensure brand consistency, e g through the Country Implementation Plan, contribute to defined brand strategy and the development of promotional tools or other relevant documentation. 
•    Collect and compile competitive intelligence in a structured way and ensure shared internally.
•    Liaise cross-functionally to set and implement strategies for new products
•    Stay up to date with internal and external developments and suggest new ways to increase sales. Keep a high scientific level in the area of Endocrinology and proactively participate or build up occasion of important scientific exchange (e.g. Congresses, education/training session) 
•     Knowledge of local market access dynamics and able to implement valuable projects for products time to the market optimization 
•    Actively advocate Immedica values and conduct all activities to highest ethical standards in accordance with country code of practice and local Laws and regulations.

Experience and competence

•    Proven work experience in Key Account Management
•    Structured collection of customer insights and competitive analysis 
•    Pursuit for sales force excellence ensuring optimal targeting and segmentation of the market.
•    Solid experience in sales and project management 
•    Demonstrable experience in negotiating and meeting clients requirements
•    In-depth understanding of sales performance metrics and the analytical skills to take relevant actions
•    Hands on experience with CRM software and MS Excel
•    Availability to travel is needed

A Scientific university degree (PhD/PharmD) is required, as well as fluency in English.  
To have obtained the expected experience and skills, we believe you have a minimum of 5 years of relevant work experience within the pharmaceutical industry. 
In addition, you have excellent analytical and organizational skills, strong communication skills and is flexible and adaptable to fit in to our growing organization.

How to apply

This is a full-time position based at our Italian affiliate. Please send in your application in English to [email protected] with the Subject line “KAM Endocrinology South / Central Italy”. Applications are reviewed on an ongoing basis, so we encourage you to apply as soon as possible

About Immedica

Immedica is pharmaceutical company, headquartered in Stockholm, Sweden, focused on the commercialization of medicines for rare diseases within metabolic, neurology, hematology & oncology and specialty care. Immedica’s capabilities cover marketing and sales, compliance, pharmacovigilance, quality assurance, regulatory and medical affairs as well as market access. Serving patients in more than 50 countries, Immedica is fully dedicated to helping those living with diseases which have a large unmet medical need.

Immedica was founded in 2018 by investment company Impilo and buy-in management and currently employs around 180 across Europe, the Middle East and the US.  Of these, approximately 80 are based in the headquarters in Stockholm. 
At Immedica, our core values are the foundation of our culture and the driving force behind how we operate, innovate, and collaborate. These values guide every decision we make, shaping our commitment to patients, partners, and colleagues. Open & Honest: We foster transparency, integrity, and trust through open communication. Effective: Focused on delivering excellence, we prioritize impact and quality to make a real difference in the rare disease landscape. Empowered: We encourage collaboration and ownership, creating a supportive workplace where all team members’ contributions drive innovation and growth. 
 

We look forward to welcoming you to the Immedica team!

Are you our next MSL in Southern Italy?

Job Title: Medical Science Liaison (MSL) Italy – Endocrinology and Metabolic Rare Diseases
Location: Italy
Employment Type: Full time

Immedica Pharma has experienced remarkable growth in recent years, and we are now looking for a MSL to further strengthen our Italian team in the south / central region.  

Immedica has rapidly evolved into a highly specialized rare disease pharmaceutical company, recognized for strong scientific expertise, impactful launches and high-value medical engagement. In line with its continued growth also in the field of Endocrinology Rare Diseases in Italy, Immedica is further strengthening its Medical Affairs organization.

We are now looking for an experienced Medical Science Liaison (MSL), a field-based scientific expert accountable for building and maintaining high-quality, long-term scientific relationships with Key Opinion Leaders (KOLs), healthcare professionals and reference centers in rare endocrine and metabolic diseases. In this role, the MSL will play a key part in the local cross-functional team, contributing to the implementation of the medical strategy through non-promotional, evidence-based scientific exchange, generation of field insights and support of clinical and scientific initiatives across the territory.

As MSL you will be also an important player in all collaboration with the Immedica Global Team, the Medical and Commercial colleagues as well as colleagues across country borders, to share knowledge, learnings and best-practices insights.

The position is field-based in Italy and reports directly to the General Manager or to the Medical Head according to the country organizational structure plan.
 

Job description and responsibilities

The MSL Italy – Endocrinology and Metabolic Rare Diseases includes
•    Bringing a strong and credible scientific presence in the field, acting as a trusted scientific partner for external stakeholders.
•    Establish, develop and maintain long-term scientific partnerships with KOLs and key stakeholders (endocrinologists, metabolic specialists, reference centers).
•    Provide high-quality, balanced and non-promotional scientific information on diseases, products, clinical data and ongoing research.
•    Drive the implementation of the local Medical Affairs strategy aligned with global medical objectives.
•    Collect, analyze and share medical insights from the field with internal stakeholders (Medical, Market Access, Commercial, R&D).
•    Identify unmet medical needs and opportunities for scientific and evidence-generation initiatives.
•    Provide scientific support to clinical trials, real-world evidence and post-marketing studies, including site and investigator engagement where appropriate.
•    Drive advisory boards, scientific meetings, congresses and educational initiatives, including preparation of scientific materials and presentations.
•    Ensure scientific training for internal teams when required (e.g. disease education,).
•    Collaborate cross-functionally while maintaining a clear non-promotional role and ensuring full compliance with internal SOPs, local regulations and industry codes.  
•    Accurately document activities and insights in approved systems (e.g. Veeva).

Experience and competence

•    Proven experience as an MSL or in Medical Affairs, preferably in Endocrinology and/or Rare Diseases. 
•    Strong understanding of the healthcare environment, clinical research and medical governance. 
•    Experience in scientific engagement with KOLs and reference centers. 
•    Excellent knowledge in health care compliance
•    Availability to travel extensively within the assigned territory. 

A Scientific university degree (MD, PhD, PharmD or MSc) in Life Sciences is required, as well as fluency in English.  
In addition, you have excellent analytical and organizational skills, strong communication skills and is flexible and adaptable to fit in to our growing organization.

How to apply

This is a full-time position based at our Italian affiliate. Please send in your application in English to [email protected] with the Subject line “MSL Italy”. Applications are reviewed on an ongoing basis, so we encourage you to apply as soon as possible.

About Immedica

Immedica is pharmaceutical company, headquartered in Stockholm, Sweden, focused on the commercialization of medicines for rare diseases within metabolic, neurology, hematology & oncology and specialty care. Immedica’s capabilities cover marketing and sales, compliance, pharmacovigilance, quality assurance, regulatory and medical affairs as well as market access. Serving patients in more than 50 countries, Immedica is fully dedicated to helping those living with diseases which have a large unmet medical need.

Immedica was founded in 2018 by investment company Impilo and buy-in management and currently employs around 180 across Europe, the Middle East and the US.  Of these, approximately 80 are based in the headquarters in Stockholm. 
At Immedica, our core values are the foundation of our culture and the driving force behind how we operate, innovate, and collaborate. These values guide every decision we make, shaping our commitment to patients, partners, and colleagues. Open & Honest: We foster transparency, integrity, and trust through open communication. Effective: Focused on delivering excellence, we prioritize impact and quality to make a real difference in the rare disease landscape. Empowered: We encourage collaboration and ownership, creating a supportive workplace where all team members’ contributions drive innovation and growth. 
We look forward to welcoming you to the Immedica team!

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