Überblick über die Statistik des Gehaltsniveaus für "QA Compliance Specialist in Deutschland"

Über das UnternehmenWir sind eine der führenden unabhängigen Sozietäten in Deutschland. Für unsere Mandanten meistern wir die komplexen Herausforderungen von heute und morgen – und bauen dabei auf die Erfahrung aus über 110 Jahren Kanzleigeschichte.Als Unterstützung für unser neu gegründetes internes Compliance-Team suchen wir in Köln einen Internal Compliance Specialist (m/w/d) mit Berufserfahrung, um gemeinsam die nächsten Schritte zu gehen. Die Rolle untersteht disziplinarisch dem Chief Operating Officer und berichtet fachlich an den Compliance-Partner.Was bieten wir Ihnen? Zusammenarbeit auf Augenhöhe in einem engagierten und sympathischen Team Abwechslungsreiche Arbeitsaufgaben in einem leistungsstarken, internationalen Arbeitsumfeld an unserem Standort in Köln Mobiles bzw. hybrides Arbeiten möglich Attraktive Verdienstmöglichkeiten Weiterbildungsangebote und Zusatzleistungen, z. B. Corporate Benefits App Regelmäßige Teamevents 30 Urlaubstage (Vollzeit) Eine freundliche "open-door-policy"Was erwartet Sie? Sie sind verantwortlich für den Aufbau und die Weiterentwicklung eines internen Compliance Competence Centers sowie eines Compliance-Management-Systems Sie konzipieren und führen Compliance- und DSGVO-Schulungen, Präventions- und Awareness-Kampagnen durch Sie setzen die KYC/AML-konforme Mandatsanlage um Sie unterstützen den Geldwäsche- und den Datenschutzbeauftragten Sie betreuen das besondere elektronische Anwaltspostfach (beA)Was sollten Sie mitbringen? Sie haben ein rechts- oder wirtschaftswissenschaftliches (Fach-)Hochschulstudium oder eine vergleichbare Qualifikation sowie erste Berufserfahrung im Compliance-, Rechts- oder Revisions-Bereich, idealerweise in einer Versicherung, Bank oder Professional Services Firm Sie besitzen Organisationstalent, Kommunikationsstärke und Teamfähigkeit und sind IT-affin und besitzen hohe Serviceorientierung sowie Interesse an Digitalisierungsthemen Sie sind einsatzbereit, verantwortungsbewusst und diskret Sie besitzen sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift (C1-Niveau) Sie beherrschen die gängigen MS-Office ProgrammeUnser Jobangebot Internal Compliance Specialist für eine Kanzlei (m/w/d)klingt vielversprechend?Bei unserem Partner Workwise ist eine Bewerbung für diesen Job in nur wenigen Minuten und ohne Anschreiben möglich. Anschließend kann der Status der Bewerbung live verfolgt werden. Wir freuen wir uns auf eine Bewerbung über Workwise. Standort Oppenhoff, Cologne

Quality Manager Partnered with an international advanced biotechnology company that have evolved into the CDMO space over the past decade, I am supporting the hire of a new Quality Manager. Due to internal promotion, this position has become available and will take a key specialist focus on all things quality, working not just on the site in Germany but also closely with the North American team. Given the increased demand on the CDMO side of the business, this role will not only take a lead on technical quality matters but will also be client facing – working with customers on a daily basis, representing the business from a QA perspective.Whilst this position will not be a line management role to begin, given the continued development of the business, progression in this company is very realistic and they are keen for individuals to shape their own pathway. Experience: Strong technical experience across operational quality processes as well as a good understanding of the wider QMSCommercial mindset – whilst you don’t need to have been customer facing, showing an understanding of this type of setting is keyDesire and ability to work in a small, flat structured team remaining hands on in all functions related to qualityFluency in English and German is essential Please apply or contact Mark Bux-Ryan to discuss further. Quality, QA, compliance, strategy, global, capa, deviation, sop, change, control, system, manufacturing, operations, bioprocessing, fermentation, cdmo, customer, client, usp, bioreactor, gmp, manager, supervisor, team, leader, specialist

Job Description This is a 1 year Fixed Term ContractHurtigruten Expeditions is the world’s leading adventure travel group, offering unique small-ship and land-based adventures from pole to pole – and anywhere in between. We take our guests to the most spectacular areas on the planet, offering a mix of pristine wilderness and visits to genuine local communities.​ This is a very exciting time to join the Hurtigruten People Experience team. The Global people team are embarking on the journey to 'Provide a People Experience that's as good as our products’.Reporting to the SVP, HX People & Culture, you will be joining a fantastic, fun, and energetic team of People Experience Partners and Operational Excellence Specialists. Together we are working on some very exciting projects that will really help us to transform the way that we work today.As the Global Head of People Operations & Experience, you play a critical role to establish and advance people services by centralising all employee transactional processing and employee relations, and implement solutions to drive compliance, performance, and quality, as well as enable and empower managers to own delivery of their employee experience. You will partner with your peers on the People & Culture Leadership Team (P&CLT) and Management to understand strategic priorities and business requirements, ensuring service delivery is continuously improved. You are a proven People Operations leader with international experience, with the ability to solve programmatically while having the scrappiness to be hands-on. As a Global Head of People Operations & Experience, HX, you’ll be responsible for: Lead a High Performing Team: You will lead, hire, engage and coach a globally dispersed team of generalists to deliver a seamless and high performing global People service; drive and inspire continuous innovation and process improvements by creating a safe space and pride in the value we add to the employee experience and to the business operations. Help the team connect to each other and the wider organisation, its objectives, while clearly prioritising for results, and driving a process excellence mindset.Define Excellence: Review the current state of People Services working practices, processes, and technology, and propose pragmatic solutions to ensure full compliance with global requirements, including defining the scope of service and defined service level agreements (SLAs). Ensure a complete process mapping of all our key processes to ensure optimised, efficient, consistent, and compliant experiences, balancing scalability with local compliance. Identify cost efficiencies through continuous improvement and workflow digitisation. Manage relevant vendor relationships, ensuring service performance and cost effectiveness.Deliver BAU on People Admin, Payroll and Benefits: Manage the administration and optimisation of day-to-day people processes, including payroll (with separate payroll teams) and benefits to ensure they are administered in a smooth and seamless manner, while fully compliant, optimising costs and employee experience. Be the point of contact for escalations ensuring service levels are met and/or exceeded and all operation metrics are trending in a positive direction.Establish a Global Compliance Baseline : Complete a full Compliance and Operational gap analysis that ensures HR guidance documents, policies, and procedures are complete, updated and aligned with our values and culture, accompanied by an educational communication program that empowers Management to make good, compliant decisions. Manage Employee Relations: Ensure strong governance on all people operations and ER cases, including resolution / re-assignment of to appropriate expert resources based on priority level, and the ER tracker is governed. Monitor re-work, case re-openings, and emerging patterns to continuously coach the team and improve processes for high performance & service. Lead or support in more complex employee relation activities including disciplinary, grievance and capability hearings including appeals and litigation. Collaborate effectively with P&CLT colleagues, other departments (including Finance and IT), and the wider business to integrate prioritisation changes, and gather & present key management information to the P&CLT and ELT (Executive Leadership Team). Regularly consult with the People function and business leaders to ensure service scope, levels and overall contribution of the teams are meeting or exceeding expectations. Support the development of a high-performance culture, ensuring performance and development practices are embedded across the organisation.

Job Description About the positionThe Quality Assurance consultant holds a vital and challenging role in any life science company: ensuring the quality and safety of products going to patients through building a Quality Management System. Finding a way to balance quality with efficiency, keeping up with the ever-changing world of new products, techniques and requirements, and intensely collaborating with various other departments and stakeholders, ...We support our clients with our profound knowledge and expertise in all quality subjects. Whether they are building a new production plant, developing new analytical methods, implementing a new quality regulation, or simply trying to solve issues and close gaps, we are there to ensure their success. Are you up for this challenge? Depending on your specific project, your role will be toBuild the Quality Management System (QMS)Discover, track and discuss problems, non-conformities and deviations within a production plant, a laboratory, a warehouse & distribution center, ...Launch, execute and document quality issues & investigationsPerform root cause analyses to determine the true source of any issueDevise CAPAs (corrective & preventive actions) to resolve the problems and prevent it from happening againCreate or improve operating procedures, work instructions, templates, quality systems, etc... To keep up with an ever-changing world.Own change controls , assessing the impact and ensuring the quality and compliance of the business throughout any changeGive trainings to operators, lab technicians, engineers, ... in your new proceduresPlan, organize and execute the review and approval of qualification reports, test protocols, validation documents, ... Together with the engineers and subject matter expertsManage or coordinate projects to implement changes within your QMSQualify, approve, monitor and periodically re-evaluate suppliersPrepare, assist and even lead internal and external auditsCollect, analyze and presentquality metrics and KPIs to determine the most strategic way forwardYour profileA University Master's degree in a relevant scientific subject (bioscience, chemistry, pharmacy, healthcare, ...)A high professional level of English and fluent in Dutch At least a first thorough QA experience in GMP environment. Depending our your seniority, the task will be adaptedMobility towards at least one of our major clients located in Puurs, Beerse, Geel, Ghent, ...A consultancy mindset :Ready to jump in a new project, quickly gain the skills and knowledge needed to support your client, and seeing any challenge as an opportunity to (im)prove yourself.Socially fluent: build your professional network at both the client and Capgemini.Business acumen: Analyze and evaluate the client's organization to identify their challenges and needs, so we can offer them solutionsKnowledge capitalization: capture and share your knowledge and expertise with other consultants and make use of Capgemini's tools to boost yourselfWhat we offerWithin Capgemini, you will be part of a global company with endless opportunities, yet we offer a very individual and personal approach and follow-up of each consultant through small teams, led by dedicated Team Managers here in Belgium.Challenging and meaningful projects, attuned to your own skills and interests, at the most renowned pharmaceutical companies in the world.The entire knowledgebase and expertise of Capgemini to support you on your projects and develop your own skills through live trainings, e-learning platforms, knowledge sharing workshops, coaching by senior consultants, etc...An extensive and transparent career framework allowing you to plan and follow your own career path: whether you want to grow into a senior consultant/expert/architect or move into Team/Account/Solution/Project Management, we are here to help you achieve your maximum potential.A highly competitive and broad salary package, including company car with fuel/energy card.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior are on the lookout for a Director for Global QA Laboratories! This position plays a vital role in tackling some of the most pressing scientific challenges of our time. Joining our team means being at the forefront of innovation, collaborating with pioneers to develop life-changing therapies that alleviate suffering and harness the power of the immune system. We're seeking someone with a deep passion for innovation, a commitment to unity, and a relentless drive to instill hope for a healthier future in countless lives. If you're ready to make a profound impact, we want to hear from you!Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesDrive a risk-based approach using modern and novel approaches to solve complex business problems.Provide expert input to functional teams in areas such as Good Clinical Laboratory Practice, GLP, ISO 15189, CAP/CLIA.Lead a team of experts and drive change initiatives in your area of expertise.Contribute to organizational quality and compliance reporting requirements.Lead the development of management reporting on quality key performance indicators.Establish and maintain regular interactions with key stakeholders to ensure quality management and governance frameworks are implemented.Collaborate with management and operational teams to adjust processes and practices as neededSet quality targets and report against those targets.Collaborate with teams to identify areas for improvement and implement quality assurance measures. RequirementsDegree in life sciences, pharmacy or equivalent.Broad and/or deep, specialized, task-specific expertise and skills.Robust understanding of Quality, GCLP/GLP/ISO 15189 principles and their impact on the company's development and business.Experience in a Quality Assurance position related to clinical laboratories.Proven team leadership experience.Ability to be agile and effectively collaborate in a dynamic, cross-functional environment.Fluency in German and English (written and spoken). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.Please note that to be considered for this role you must have the right to work in this location. Key ResponsibilitiesCollaborate with key stakeholders in portfolio and study teams to detect and remediate risks.Provide guidance on day-to-day questions arising from clinical trials deliverables.Interact with CROs to ensure adequate quality oversight on clinical activities.Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.Support inspections preparation and facilitation in collaboration with other QA groups.Support audits and inspections as well as follow-up activities including CAPA preparations.RequirementsKnowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.An academic degree in Life Science (advanced degree preferred). Apply nowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.