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Academic Resource söker en Kvalitetsingenjör / QC till ett läkemedelsföretag i Uppsala.

Tjänsten är en rekrytering för kunds räkning.

Arbetet är på heltid och dagtid. Placering i Uppsala.

Start omgående.

Kemilaboratoriet ansvarar för kontroll av slutprodukt samt förpackningsmaterial och deltar i flertalet utvecklingsprojekt. De dominerande analysteknikerna på laboratoriet är kromatografi, spektroskopi, våtkemi och mikroskopi.

Arbetsuppgifter:

Som Kvalitetsingenjör ansvarar du självständigt för ett större arbetsområde där du planerar ditt arbete, driver utredningar av incidenter och representerar avdelningen i projekt, förbättringsarbete och avvikelseutredningar. Rollen innebär metod- och/eller instrumentansvar för mer avancerade analystekniker inklusive kvalificering- och valideringsaktiviteter. Du sammanställer och rapporterar resultat, genomför försöksplaner och analyser samt skriver och granskar dokumentation med hög noggrannhet.

Du kommer även att arbeta med:

• Planera självständigt sitt arbete inom givna ramar

• Initiera och utreda incidenter och event

• Fungera som avdelningens representant i projektgrupper eller avvikelseutredningar

• Ha metodansvar för tyngre tekniker och rumsansvar

• Delta aktivt i förbättringsarbetet inom avdelningen

• Sammanställa, kontrollera och rapportera resultat

• Utföra rutinarbete och genomföra försöksplaner efter avdelningens behov

• Skriva och granska självständigt rapporter, försöksplaner och annan dokumentation åt sektionen

• Fungera som handledare för andra medarbetare inom och utanför sektionen

• Genomföra självständigt utvecklingsarbete och felsökning

Kvalifikationer:

• Minst treårig högskoleutbildning med naturvetenskaplig/teknisk inriktning

• Minst 5 år erfarenhet av arbete inom GMP-reglerad verksamhet

• Minst 5 års erfarenhet inom QC

• Avancerad svenska i tal och skrift (nivå C1)

• Fullständig behärskning av engelska i tal och skrift (nivå C2)

• Goda PC-kunskaper

Vi söker dig som är noggrann, kommunikativ och trivs i en roll där problemlösning är en naturlig del av vardagen. Du har lång erfarenhet av att arbeta enligt GMP och säkerställer hög kvalitet i både analys, dokumentation och kvalificeringsarbete.

Ansökan:

Intervjuer och urval kommer att ske löpande, så skicka gärna din ansökan så snart som möjligt.

Klicka nedan på sök tjänsten och fyll i dina kontaktuppgifter, ange referensnamn: FKI0826

we take you further

Academic Resource söker en Kvalitetsingenjör / QC till ett läkemedelsföretag i Uppsala.

Tjänsten är en rekrytering för kunds räkning.

Arbetet är på heltid och dagtid. Placering i Uppsala.

Start omgående.

Kemilaboratoriet ansvarar för kontroll av slutprodukt samt förpackningsmaterial och deltar i flertalet utvecklingsprojekt. De dominerande analysteknikerna på laboratoriet är kromatografi, spektroskopi, våtkemi och mikroskopi.

Arbetsuppgifter:

Som Kvalitetsingenjör ansvarar du självständigt för ett större arbetsområde där du planerar ditt arbete, driver utredningar av incidenter och representerar avdelningen i projekt, förbättringsarbete och avvikelseutredningar. Rollen innebär metod- och/eller instrumentansvar för mer avancerade analystekniker inklusive kvalificering- och valideringsaktiviteter. Du sammanställer och rapporterar resultat, genomför försöksplaner och analyser samt skriver och granskar dokumentation med hög noggrannhet.

Du kommer även att arbeta med:

• Planera självständigt sitt arbete inom givna ramar

• Initiera och utreda incidenter och event

• Fungera som avdelningens representant i projektgrupper eller avvikelseutredningar

• Ha metodansvar för tyngre tekniker och rumsansvar

• Delta aktivt i förbättringsarbetet inom avdelningen

• Sammanställa, kontrollera och rapportera resultat

• Utföra rutinarbete och genomföra försöksplaner efter avdelningens behov

• Skriva och granska självständigt rapporter, försöksplaner och annan dokumentation åt sektionen

• Fungera som handledare för andra medarbetare inom och utanför sektionen

• Genomföra självständigt utvecklingsarbete och felsökning

Kvalifikationer:

• Minst treårig högskoleutbildning med naturvetenskaplig/teknisk inriktning

• Minst 5 år erfarenhet av arbete inom GMP-reglerad verksamhet

• Minst 5 års erfarenhet inom QC

• Avancerad svenska i tal och skrift (nivå C1)

• Fullständig behärskning av engelska i tal och skrift (nivå C2)

• Goda PC-kunskaper

Vi söker dig som är noggrann, kommunikativ och trivs i en roll där problemlösning är en naturlig del av vardagen. Du har lång erfarenhet av att arbeta enligt GMP och säkerställer hög kvalitet i både analys, dokumentation och kvalificeringsarbete.

Ansökan:

Intervjuer och urval kommer att ske löpande, så skicka gärna din ansökan så snart som möjligt.

Klicka nedan på sök tjänsten och fyll i dina kontaktuppgifter, ange referensnamn: FKI0826

we take you further

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.  

The key responsibility of the Quality Control technician is for  receiving  and analyzing test material, incoming parts, product intermediates and finalized products for Research & Development, Testing & Validation, and Production using a range of instruments as well as participating in problem solving and technical troubleshooting exercises on the execution side.  

Key Responsibilities

Key responsibilities include (but are not limited to) 

• Execute work instructions and participate in laboratory functions/tasks/work.  
• Follow 5S and safety protocols within the production and laboratory work environment.
• Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples in the expected template and/or Laboratory Information Management System (LIMS); and maintain control charts. 
• Able to understand and execute testing and validation plans for incoming parts, product intermediates, finalized products, and other material accordingly.
• Identify problems with test material, analysis methods, and instrumentation.  
• Be able to troubleshoot basic to advance problems; utilizing the help of suppliers or experts for more major issues.  
• Understand the fundamental principles of method development and/or method validation and able to participate in the execution.  
• Able to write support documentation for standard operations. 
• Maintaining instruments and measurement areas to a high standard, involving responsibility to ensure that the laboratory or production room(s)/area(s) comply with safety related guidelines, 5S guidelines, maintaining consumable inventory and instrument readiness. 
• Able to train and qualifying personnel according to a skill and competence level.
• Strict adherence to Quality Assurance and Quality Control Principles.  
• Participate in improvement plans and investigations for various topics.  

Accountability/Authorization

• Budget responsibility: No 
• Direct reports: No 
• Work Environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role.

Qualifications and experience 

• Bachelor´s degree or master’s degree in a technical field is preferred. 
• 2 years experience in quality control from relevant industry is preferred.
• Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. (preferred)
• Familiar with quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM).
• Familiar with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma, Quality troubleshooting tools and problem-solving methodology. (Preferred) 
• Curious, technically educated and preferably with a strong business background.
• Experience in Cell Manufacturing, or Test and Validation is an advantage. 

Specific skills & Knowledge

• Knowledge of Laboratory Information Management Systems (LIMS) or other sample tracking software is a plus. 
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams. 
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform manual labor in physically demanding environments. This can include 100% working hours allocation into clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs. This role requires working full-time on the shop floor, supporting operation.