Anocca AB jobb

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 20 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. Prior experience of working in a GMP environment, either in close collaboration with Quality Assurance departments or within Quality Assurance, 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) • Experience working according to GMP • 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 analytical engineer to join and strengthen the QC team which consists of one scientist, one senior analytical engineer (recruitment ongoing) one analytical engineer and one process technician. The QC team is part of the larger GMP operations team consisting of a production team, QA managers, facility manager, application specialist, for a total of 20 colleagues. You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials. You will also participate in environmental monitoring sampling, raw material control, deviation investigations and review of documentation. Experience in cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis. Knowledge of aseptic work techniques is desirable. Prior experience working in a GMP environment is preferred for the role. 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 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: • Experience working according to GMP. • Quality control experience in the cell therapy or ATMP space. • Experienced in writing deviation investigations, CC and CAPA’s. • Good grasp of the underlying biology related to cell engineering. • Experience in microbiology. • 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. Please note that we contact candidates that we would like to invite for an interview within 3 weeks after the advertisement has closed. Unsuccessful candidates will not be contacted. Compensation Monthly salary Tier 1 occupational pension plan Wellness grant Flexible work hours We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.

Join Our Team as a Bioengineer! We are currently seeking a highly motivated Bioengineer to join our dynamic team. In your role as Bioengineer, you will play a crucial role in ensuring the efficiency and effectiveness of our processes. If you have a passion for technology and a keen eye for detail, we encourage you to apply. About the RoleWe are looking for a highly motivated Bioengineer to join our Specimen Core. You will be involved in research projects employing cutting edge technologies, and state of the art equipment. The Bioengineer role at Anocca is a junior role for graduates with a keen interest in biotechnology and life sciences. As a part of Specimen Core you will contribute to Anocca’s operations by isolation and banking of cells from blood specimens, including their genetic and phenotypic characterisation. You will also support operations with equipment maintenance and service. Being a part of our Specimen Core includes routine handling of incoming blood: PBMC isolation from blood and banking DNA extraction from cells Phenotypic analysis of cells by flow cytometry What We're Looking For: Molecular biology laboratory skills Experience in working with primary human cells Good time management skills and proficient in data documentation Fluent written and spoken English It would be nice if you have: Experience with handling blood Experience in gene-editing technologies Experience of quality system driven operations (ISO, GxP or equivalent) Why us: Our company is at the forefront of technological innovation, striving to make a difference in the industry. We offer a dynamic working environment where talent and ambition are recognized and rewarded. Join us, and be part of a team that values growth, collaboration, and the pursuit of excellence. We Offer: Competitive salary and benefits package. Opportunities for professional development and career advancement. A collaborative and supportive work culture. State-of-the-art facilities and resources. How to Apply:If this position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter. 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.

Join Our Team as a Laboratory Technician! We are currently seeking highly motivated Laboratory Technician to join our dynamic team. In your role as Technician, you will play a crucial role in ensuring the efficiency and effectiveness of our processes. If you have a passion for technology and a keen eye for detail, we encourage you to apply. About the RoleWe are looking for a highly motivated Lab Tech to join our Specimen Core. You will be involved in research projects employing cutting edge technologies, and state of the art equipment. The Laboratory Technician role at Anocca is a junior role for graduates with a keen interest in biotechnology and life sciences. As a part of Specimen Core you will contribute to Anocca’s operations by isolation and banking of cells from blood specimens, including their genetic and phenotypic characterisation. You will also support operations with equipment maintenance and service. Being a part of our Specimen Core includes routine handling of incoming blood: PBMC isolation from blood and banking DNA extraction from cells Phenotyping of cells by flow cytometry What We're Looking For: Molecular biology laboratory skills Good time management skills and proficient in data documentation Fluent written and spoken English It would be nice if you have: Experience with handling blood Some experience of working with primary cells Experience of quality system driven operations (ISO, GxP or equivalent) Why us: Our company is at the forefront of technological innovation, striving to make a difference in the industry. We offer a dynamic working environment where talent and ambition are recognized and rewarded. Join us, and be part of a team that values growth, collaboration, and the pursuit of excellence. We Offer: Competitive salary and benefits package. Opportunities for professional development and career advancement. A collaborative and supportive work culture. State-of-the-art facilities and resources. How to Apply:If this position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter. Join us in making a difference, apply now!

Join Our Team as a Process Engineer We are currently seeking experienced and motivated Process Engineers to join our dynamic team. As a pivotal part of our operations, the Process Engineer will play a crucial role in ensuring the efficiency and effectiveness of our processes. If you have a passion for technology and a keen eye for detail, we encourage you to apply. About the RoleAs a Process Engineer, you will be involved in the manufacturing of ATMP products, to be used in clinical trials. The role at Anocca is suited to experienced and motivated professionals with a drive to lead and execute by action. Experience in aseptic work, including processing of ATMPs, as well as in electronic batch management systems would be a significant asset. You should have high-quality relevant experience, excellent English communication skills, knowledge of aseptic manufacturing techniques, and be securely anchored in GMP regulations. You must be capable of working as part of a team but should also demonstrate initiative to drive projects forward. What We're Looking For: Manufacturing experience in the cell therapy or ATMP space Significant and relevant experience in cell processing equipment and validation Good grasp of the underlying biology, preferably experience in T-cell immunology Fluent written and spoken English Why Join Us? Our company is at the forefront of technological innovation, striving to make a difference in the industry. We offer a dynamic working environment where talent and ambition are recognized and rewarded. Join us, and be part of a team that values growth, collaboration, and the pursuit of excellence. We Offer: Competitive salary and benefits package. Opportunities for professional development and career advancement. A collaborative and supportive work culture. State-of-the-art facilities and resources. How to Apply: If this Process Engineer 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 may use background checks in the recruiting process.

Job description: We are looking for a full time senior analytical engineer to join and strengthen the QC team which consists of one scientist, 2 analytical engineers and 1 process technician. The QC team is part of the larger GMP operations team consisting of a production team, QA managers, facility manager, application specialist, for a total of 20 colleagues. You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials. You will also take a leading role in deviation investigations and review of documentation. Experience of cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis. Knowledge of aseptic manufacturing techniques is desirable. Prior experience working in a GMP environment is essential for the role. You must be capable of working as part of a team and demonstrate initiative to drive projects forward. As the company and team is very international and the business language is English, excellent English communication skills is required. The role is suited to experienced and motivated professionals with a drive to lead and execute by action. What we are looking for: • Experience working according to GMP.• Quality control experience in the cell therapy or ATMP space.• Significant and relevant experience in instrument and method validation.• Experienced in writing and leading deviation investigations, CC and CAPA’s.• Good grasp of the underlying biology related to cell engineering.• Experience in microbiology.• 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. Please note that we contact candidates that we would like to invite for an interview within 3 weeks after the advertisement has closed. Unsuccessful candidates will not be contacted.Compensation Monthly salaryTier 1 occupational pension planWellness grantFlexible work hours When to apply:Last day to apply 2025-03-31EmployerAnocca AB(org.nr 556946-2384)