Lediga jobb SHL Medical AB i Nacka

Process Mining Specialist
SHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that require innovative devices such as auto-injectors or pen injectors to effectively deliver their drugs. Headquartered in Switzerland since late 2018, with sites in Sweden, Taiwan, and the United States.
Job Overview
The Process Mining Specialist will play an exciting role in the technical deployment of SHL Medical’s Process Mining initiatives within the global Process Excellence team. The role will be both business and IT facing and will ensure that our process mining activities are aligned with SHL Medical’s fast growth as well as well embedded in other process-related projects.
Your place of work will be in Stockholm, Sweden, where the Process Excellence Centre of Excellence is located, and you will work together with a global team of process experts from Switzerland, Taiwan and US.
Main Responsibilities
Developing, modifying, and validating data extraction and transformation scripts.
Removing corrupted data and fixing coding errors and related problems.
Performing analysis to assess quality and meaning of data.
Filtering data by reviewing reports and process performance indicators (PPIs) to identify and correct code problems.
Using statistical tools to identify, analyse, and interpret patterns and trends in complex data sets that could be helpful for the diagnosis and prediction.
Preparing analysis reports based on stakeholders’ requirements, enabling them to take informed decisions.
Supporting the development, analysis, and improvement of business processes.


Skills and Qualification

Bachelor’s Degree (or higher) in Business Information Technologies, Information Sciences, Business Informatics, Data Science, Computer Science or Business Administration.
2+ years of professional experience in process mining.
Solid experience in with regards to data transformation and data analytics, as well as database technologies, ETL, and programming (e.g., Java, Python and R).
Solid understanding of process management concepts, BPM technology, and familiarity with process modeling standards, ideally BPMN 2.0.
Experience working with ERP systems (ideally SAP), data extraction, data analysis, reporting, etc.
Proficiency in statistics and statistical packages (e.g., Excel, SPSS, SAS and R) to be used for data set analysing.
Experience in data visualization (e.g., using Tableau, Qlik or PowerBI).
Understanding of key customer processes, such as Order-to-Cash, Procure-to-Pay, Invoice-to-Cash, Invoice-Pay, Plan-to-Produce, Issue-to-Resolution, etc. and their typical improvement potentials.
Value quality, accuracy, and attention to detail.
Team-working skills for cross-functional, cross-cultural collaboration as well as an ability to work with minimal supervision.
Excellent verbal and written communication skills in English.
Critical thinking, and a systematic and logical approach to problem-solving.
Ability to travel outside of Europe.
SAP Signavio experience preferred.
PLM experience preferred.
MedTech experience preferred.


We Offer
An exciting opportunity in a fast-growing international medical device company.
Being part of a highly motivated Process Excellence team, closely integrated into the business.
A modern working environment, with multicultural and dynamic teams.
Flexible working hours and a hybrid remote work policy.
Challenging assignments in an innovative industry.
Position in a dynamic, international team of highly skilled professionals.
Various opportunities for personal and professional development within a global organization.


Interested in joining SHL Medical and in supporting us with your expertise and personality? Then we look forward to receiving your application including your CV, motivation letter, and all other relevant documents to our Talent Acquisition Department at [email protected]
Please note: For this position, we do not consider applications from recruitment agencies. Visa mindre

SHL Medical AB, part of SHL Medical, offers you a position in a dynamic environment where we develop and manufacture products that improve people’s health and quality of life. We are now looking for a Specialist Regulatory Affairs for our office in Nacka Strand, Stockholm.
As a Specialist within Regulatory Affairs, you will be part of a team of 3 highly skilled specialists in Nacka Strand, and many more globally. Main focus will be to contribute to and support various development projects, throughout the product life cycle. This means interacting with most functions and departments at SHL Medical AB, such as Product Development, Project Management and Quality Assurance. You will also be in contact with and provide support to customers and their RA representatives, as well as internally with our SHL colleagues in Taiwan, US and Switzerland.
As a Specialist Regulatory Affairs, you carry out various work tasks, for example:
Act as company liaison with regulatory health authorities. Develop regulatory strategic plans specific to development programs.
Lead and author delivery of regulatory submission dossiers. Drive and implement process and system improvements to ensure successful submission outcomes.
Ensure applicable regulations and standards are integrated within the organization by e.g. participate in standardization organizations.
Guide the organization including management teams to ensure that SHL complies with up-to-date regulations and standards pertaining medical device and other products or services.
Management of SHL's certificates, authorizations, device registration etc.
Provide input for regulatory requirements and regulatory strategies in interdepartmental meetings on product development to ensure timely submission and approval.
Acting as coordinator and/or single contact point < SHL-Customer/Authority > in submission process.
Directly involved in the preparation, assembly and submission of all global regulatory documents, such as MAF, CTD and other international regulatory submissions in various countries.

We see that you have a background within QARA, and that you have a MsC or corresponding work experience. You are fluent in English, in speech and writing. We highly value experience within the medical device field. You have strong communication skills and have the will and ability to work and collaborate in a global company.
Would you like to know more? Please visit our website or follow us on LinkedIn.
We welcome your application! Visa mindre

Would you like to develop long term as part of a growth company, which continuously strengthens its position through innovative products? Then this is the position for you!
SHL Medical AB, part of SHL Medical, offers you a position in a dynamic environment where we develop and manufacture products that improve people’s health and quality of life. As an employee you take a great responsibility and join a global organization at an expanding stage. We are now seeking a Senior Specialist Regulatory Affairs for our office in Nacka Strand, Stockholm.
As a Senior Specialist within Regulatory Affairs, you will be part of a team of 3 highly skilled people and you will work closely together with the Quality Assurance team. Main focus will be to contribute to and support various development projects, throughout the product life cycle. This means interacting with most functions and departments at SHL Medical AB, such as Product Development, Project Management, Innovation, Business Development and so on. You will also be in contact with and provide support to customers and their RA representatives, as well as internally with our SHL colleagues in Taiwan, US and Switzerland.
As a Senior Specialist Regulatory Affairs, you carry out various work tasks, for example:
Act as company liaison with regulatory health authorities. Develop regulatory strategic plans specific to development programs.
Lead and author delivery of regulatory submission dossiers. Drive and implement process and system improvements to ensure successful submission outcomes.
Ensure applicable regulations and standards are integrated within the organization by e.g. participate in standardization organizations.
Guide the organization including management teams to ensure that SHL complies with up-to-date regulations and standards pertaining medical device and other products or services.
Management of SHL's certificates, authorizations, device registration etc.
Provide input for regulatory requirements and regulatory strategies in interdepartmental meetings on product development to ensure timely submission and approval.
Acting as coordinator and/or single contact point < SHL-Customer/Authority > in submission process.
Directly involved in the preparation, assembly and submission of all global regulatory documents, such as MAF, CTD and other international regulatory submissions in various countries.

We see that you have a background within QARA, and that you have a MsC or corresponding work experience. You are fluent in English, in speech and writing. We highly value experience within the medical device field and/or experience from working with pharmaceutical companies. You have strong communication skills and have the will and ability to work and collaborate in a global company.
Would you like to know more? Please visit our website or follow us on LinkedIn.
We welcome your application! Visa mindre