QA Manager
Anocca ABSammanfattning
Anocca is seeking a full-time Quality Assurance Manager to enhance its GMP Operations team, which consists of around 30 professionals. The role involves overseeing quality assurance activities, including document approval, deviation investigations, and validation of methods for ATMP products used in clinical trials. Strong English communication skills are essential, and the position is ideal for motivated individuals eager to grow in a dynamic environment.Jobbet i korthet
Anställningstyp
tillsvidareanstallning
Arbetstid
heltid
Det här erbjuder vi
International workplace with job varietyInteraction with all Anocca employeesOpportunity to work at the intersection of biotechnology and medicineMonthly salaryTier 1 occupational pension planWellness grantFlexible work hours
Ansök senast: 2026-12-31
Publicerad: 2026-10-12
Beskrivning
Join Our Team as a QA Manager
We are looking for a full time Quality Assurance Manager to join and strengthen the GMP Operations team at Anocca.
The GMP operations team currently consist of a production team, a QC team, QA managers including QP, facility manager, validation and project managers, for a total of approximately 30 colleagues.
You will be involved in the quality assurance of all operative activities, including document approval, deviation investigations, material release, training of employees, validation of equipment, maintenance of the Quality Management System (QMS) and validation of methods for release of ATMP products, to be used in clinical trials. Also, document administration will be an important part of this role.
Previous experience in Quality Assurance (QA) within a GMP environment is required for this role'
Experience in regulatory guidelines for ATMP (EudraLex Vol.4), aseptic work (EudraLex Annex 1) or in microbiology would be a significant asset.
You must be capable of working as part of a team and as the company and team is very international and the business language is English, excellent English communication skills both in speech and in writing is required.
The role is suited to motivated persons with a drive to learn and grow in a complex and varied environment.
What we are looking for:
• BSc or MSc in life science subject (biology, pharmacy, chemistry or similar)
• Previous experience in QA role
• Meticulous documentation administration skills
• Experienced in deviation investigations, CC and CAPAs
• Fluent written and spoken English
We offer:
An international workplace with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine.
Compensation:
• Monthly salary
• Tier 1 occupational pension plan
• Wellness grant
• Flexible work hours
How to Apply:
If this QA position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter, through our careers portal. Join us in making a difference, apply now!
We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.
We are looking for a full time Quality Assurance Manager to join and strengthen the GMP Operations team at Anocca.
The GMP operations team currently consist of a production team, a QC team, QA managers including QP, facility manager, validation and project managers, for a total of approximately 30 colleagues.
You will be involved in the quality assurance of all operative activities, including document approval, deviation investigations, material release, training of employees, validation of equipment, maintenance of the Quality Management System (QMS) and validation of methods for release of ATMP products, to be used in clinical trials. Also, document administration will be an important part of this role.
Previous experience in Quality Assurance (QA) within a GMP environment is required for this role'
Experience in regulatory guidelines for ATMP (EudraLex Vol.4), aseptic work (EudraLex Annex 1) or in microbiology would be a significant asset.
You must be capable of working as part of a team and as the company and team is very international and the business language is English, excellent English communication skills both in speech and in writing is required.
The role is suited to motivated persons with a drive to learn and grow in a complex and varied environment.
What we are looking for:
• BSc or MSc in life science subject (biology, pharmacy, chemistry or similar)
• Previous experience in QA role
• Meticulous documentation administration skills
• Experienced in deviation investigations, CC and CAPAs
• Fluent written and spoken English
We offer:
An international workplace with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine.
Compensation:
• Monthly salary
• Tier 1 occupational pension plan
• Wellness grant
• Flexible work hours
How to Apply:
If this QA position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter, through our careers portal. Join us in making a difference, apply now!
We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.
Ansök till tjänsten
QA Manager
OM FÖRETAGET
Anocca AB
