Chemistry Quality Control Manager
GE Healthcare
Job Description SummaryJoin Our Quality Control Management Team – Oslo Site
Are you passionate about maintaining the highest standards in pharmaceutical manufacturing? At our Oslo site, we produce contrast agents—critical medicines used in medical imaging diagnostics worldwide.
Quality Control (QC) is a key support function at the Oslo Plant, ensuring product quality at every stage of the manufacturing process and compliance with GMP standards. We are proud to contribute to global patient safety and are now seeking one experienced manager to lead one of our QC Chemistry departments and strengthening our QC leadership team.
QC Oslo consists of six specialized departments:
•\tTwo Microbiology departments
•\tOne Systems department
•\tThree Chemistry departmentsJob DescriptionKey ResponsibilitiesDaily Management & ResourcesLead daily operations and guide your team in product analysis.Collaborate with production and global teams to resolve abnormal results.Ensure efficient workflows and a positive team environment.Optimize resource use and apply the principles of the Daily Management System (DMS).Training & DevelopmentEnsure team members are properly trained and competent.Maintain updated job descriptions and authorization records.Support employee growth through tailored challenges and development plans.Stay informed on industry developments and contribute to department strategy.Quality & ComplianceImplement and maintain test methods and documentation.Ensure products and equipment meet quality standards before release.Monitor handling of semi-finished products and ensure safety compliance.Review and approve GMP documents, SOPs, nonconformities, and batch records.Support preparation of PQR reports, quality metrics, and change control processes.Lean & ImprovementLead with a LEAN mindset, initiate LEAN activities and actively drive continuous improvement across the department.EHS (Environment, Health & Safety)Ensure EHS compliance and lead preventive efforts within your area.Promote a safe, respectful, and motivating work environment.Follow safety procedures and encourage a culture of responsibility and care.QualificationsStrong leadership and management skillsExcellent problem-solving and analytical abilitiesThorough understanding of QC principles and techniquesEffective communication and interpersonal skillsFamiliarity with industry regulations and standards (GxP)Minimum 5 years of experience in quality controlRecommended minimum 3 years of experience in the pharmaceutical industryInclusion & Diversity
Are you passionate about maintaining the highest standards in pharmaceutical manufacturing? At our Oslo site, we produce contrast agents—critical medicines used in medical imaging diagnostics worldwide.
Quality Control (QC) is a key support function at the Oslo Plant, ensuring product quality at every stage of the manufacturing process and compliance with GMP standards. We are proud to contribute to global patient safety and are now seeking one experienced manager to lead one of our QC Chemistry departments and strengthening our QC leadership team.
QC Oslo consists of six specialized departments:
•\tTwo Microbiology departments
•\tOne Systems department
•\tThree Chemistry departmentsJob DescriptionKey ResponsibilitiesDaily Management & ResourcesLead daily operations and guide your team in product analysis.Collaborate with production and global teams to resolve abnormal results.Ensure efficient workflows and a positive team environment.Optimize resource use and apply the principles of the Daily Management System (DMS).Training & DevelopmentEnsure team members are properly trained and competent.Maintain updated job descriptions and authorization records.Support employee growth through tailored challenges and development plans.Stay informed on industry developments and contribute to department strategy.Quality & ComplianceImplement and maintain test methods and documentation.Ensure products and equipment meet quality standards before release.Monitor handling of semi-finished products and ensure safety compliance.Review and approve GMP documents, SOPs, nonconformities, and batch records.Support preparation of PQR reports, quality metrics, and change control processes.Lean & ImprovementLead with a LEAN mindset, initiate LEAN activities and actively drive continuous improvement across the department.EHS (Environment, Health & Safety)Ensure EHS compliance and lead preventive efforts within your area.Promote a safe, respectful, and motivating work environment.Follow safety procedures and encourage a culture of responsibility and care.QualificationsStrong leadership and management skillsExcellent problem-solving and analytical abilitiesThorough understanding of QC principles and techniquesEffective communication and interpersonal skillsFamiliarity with industry regulations and standards (GxP)Minimum 5 years of experience in quality controlRecommended minimum 3 years of experience in the pharmaceutical industryInclusion & Diversity
We are proud to be an Equal Opportunity Employer. We value diversity and are committed to creating an inclusive environment for all employees.
We are also proud signatories of the Armed Forces Covenant and actively welcome applications from Armed Forces Engineers, veterans, and reservists. Your skills, discipline, and experience are highly valued here.
Total RewardsWe offer a competitive salary and benefits package designed to support your ambitions and well-being. You’ll also have access to global career development opportunities in a culture that fosters innovation and support.
Ready to make a difference in healthcare?Apply now and be part of a team that’s transforming lives through technology. Creating a World where Healthcare has no limits.
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Additional InformationRelocation Assistance Provided: No
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