165 Jobs für Pharmaceutical Quality Assurance
Stellenangebote Pharmaceutical Quality Assurance Jobs
Job vor 3 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] Schwerbehinderung und ihnen Gleichgestellte werden bei gleicher Eignung bevorzugt eingestellt. Required Skills: Accountability, Adaptability, Business Process Creation, c GMP Compliance, Data Analysis, Decision Making, Documentation Review, Documentations, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Interpersonal Relationships, IS Audit, Pharmaceutical Quality Assurance, Pharmaceutical Quality Control (QC) , Pharmaceutical Systems, Process Management, Process Operations, Process Standardization, Product Quality Assurance, Quality Inspections, Quality Management, Quality Management System Auditing, Quality Operations, Quality Standards, Regulatory Compliance, Regulatory Inspections Preferred Skills: Search Firm Representatives Please Read Carefully Merck Co. , Inc. , Rahway, NJ, USA, also known [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Specialist In-Market Quality (m/w/d)
• München, Bayern
[. .. ] mit Schwerbehinderung und ihnen Gleichgestellte werden bei gleicher Eignung bevorzugt eingestellt. Required Skills:Accountability, Adaptability, Business Process Creation, c GMP Compliance, Data Analysis, Decision Making, Documentation Review, Documentations, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Interpersonal Relationships, IS Audit, Pharmaceutical Quality Assurance, Pharmaceutical Quality Control (QC) , Pharmaceutical Systems, Process Management, Process Operations, Process Standardization, Product Quality Assurance, Quality Inspections, Quality Management, Quality Management System Auditing, Quality Operations, Quality Standards, Regulatory Compliance, Regulatory Inspections Preferred Skills:Current Employees apply Current Contingent Workers apply Search Firm Representatives Please Read Carefully Merck Co. , Inc. [. .. ]
Job vor 9 Tagen bei Jobware gefunden
Fresenius Kabi Deutschland GmbH
• Bad Homburg
[. .. ] in Packaging. This global position offers a unique opportunity to collaborate across borders and drive continuous improvement in supplier relationships. Your assignments Select and qualify packaging suppliers [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to ensure high-quality materials. Collaborate with suppliers to choose optimal packaging for Fresenius Kabis products. Lead global harmonization projects to standardize packaging specifications and processes. Coordinate closely with international stakeholders from Operations Units and Innovation Development to identify synergies in our portfolio and run projects to bring global packaging components to the next [. .. ] Your profile Academic background in (Packaging) Engineering, Material Science, or a related technical field, complemented by 3-5 years of relevant industry experience in packaging related development, production, or quality assurance within the pharmaceutical or medical device sector. Extensive expertise in packaging production technologies and understanding of associated packaging defects. This position will support selected packaging categories, e. g. glass, rubber stoppers, thermoplastics, foils, printed packaging. Strong background in assessing primary packaging interactions with products, supported by experience in extractables and leachable studies. Competencies [. .. ]
Job vor 9 Tagen bei JobMESH gefunden
Fresenius Kabi Deutschland GmbH
(Senior) Manager (m/f/d) Supplier Compliance Management Packaging (Technical Packaging Expert)
• Hesse Bad Homburg
[. .. ] in Packaging. This global position offers a unique opportunity to collaborate across borders and drive continuous improvement in supplier relationships. Your assignments Select and qualify packaging suppliers [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to ensure high-quality materials. Collaborate with suppliers to choose optimal packaging for Fresenius Kabi s products. Lead global harmonization projects to standardize packaging specifications and processes. Coordinate closely with international stakeholders from Operations Units and Innovation Development to identify synergies in our portfolio and run projects to bring global packaging components to the [. .. ] Your profile Academic background in (Packaging) Engineering, Material Science, or a related technical field, complemented by 3-5 years of relevant industry experience in packaging related development, production, or quality assurance within the pharmaceutical or medical device sector. Extensive expertise in packaging production technologies and understanding of associated packaging defects. This position will support selected packaging categories, e. g. glass, rubber stoppers, thermoplastics, foils, printed packaging. Strong background in assessing primary packaging interactions with products, supported by experience in extractables and leachable studies. Competencies [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Niedersachsen
Führungs-/ Leitungspositionen
[. .. ] Arbeitsumfeld Start: Schnellstmöglich Interessiert? Dann freuen wir uns auf Ihre aussagekräftigen Bewerbungsunterlagen mit Angabe Ihrer Gehaltsvorstellung und des frühestmöglichen Eintrittstermins. Gerne an oder hier auf Linked In. [...]
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[...] #Qualitätsmanagement #Quality Management #Pharma #GMP #Quality Sicherung #Quality Assurance #Regulatory Affairs #Führungsposition #Chemie #Chemistry #Jobs Norddeutschland #Jobs In Pharma #Quality Control #Familienunternehmen #Karriere #Stellenangebot Pharma #Pharmaceutical Industry #QM Leitung #Head Of Quality #Jobsin Chemie #J-18808-Ljbffr 72522209 [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Principal Business Consultant-R D-Regulatory (Remote)
Beratungs-/ Consultingtätigkeiten
[. .. ] and thought leadership that differentiate R D consulting in the market Lead multiple project engagement teams empowering the team to plan and manage all aspects of delivery, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] from scope to quality assurance Requirements Significant management and R D consulting experience (at least 10 years) Experience in the Life Sciences, particularly in Regulatory Affairs and Regulatory Information Management An extensive network of relevant stakeholders within leadership positions in Top 20 Life Sciences companies Credibility and experience in operating and engaging at senior levels [. .. ] contact us at Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Consulting Industries Software Development, IT Services and IT Consulting, and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Veeva Systems by 2x Get notified about new Principal Business Consultant jobs in Germany. Business-Development-Manager (m/w/d) Business Development Manager/ Partnermanager (m/w/d) Business Development Manager (all genders) Business Development Manager Aerospace (m/w/d) Freelance Business Development [. .. ]
Job am 03.11.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] clinical trial medications. A unique opportunity to shape the future of the company and contribute to strategic decisions The chance to work in an innovative and growing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field: clinical supply, pharmaceutical process development, and New Product Introduction A dynamic and young working environment with daily challenges A highly enriching and versatile role Flexible work arrangements, including the possibility of remote work Opportunities for working in an international group with multiple locations worldwide Your profile University degree (masters level or equivalent) in [. .. ] systems, process development, facilities, equipment, and utilities In-depth knowledge of aseptic processing and technology/ product transfers Strong understanding of regulatory requirements: US FDA, EMA, Swissmedic Proven leadership experience in quality assurance Advanced analytical skills, data-driven, with a focus on continuous improvement Excellent cross-functional teamworking communication skills Comfortable working in a demanding international environment Fluent in French and English (spoken and written) Contact If you recognize yourself in this profile, feel free to send us your complete application at: We [. .. ]
Job am 08.10.2025 bei Jobleads gefunden
Principal Business Consultant-R D-Clinical (Remote)
Beratungs-/ Consultingtätigkeiten
[. .. ] and thought leadership that differentiate R D consulting in the market Lead multiple project engagement teams-empowering the team to plan and manage all aspects of delivery, from [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scope to quality assurance Requirements Significant management and R D consulting experience (at least 10 years) Experience in the Life Sciences, particularly in the clinical operations area Extensive network of relevant stakeholders within leadership positions in Top 20 Life Sciences companies Credibility and experience in operating and engaging at senior levels with key Life [. .. ] contact us at Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Consulting Industries Software Development, IT Services and IT Consulting, and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Veeva Systems by 2x Sign in to set job alerts for Principal Business Consultant roles. Freelance Business Development Manager (m/f/d) Business-Development-Manager (m/w/d) Business Development Manager/ Partnermanager (m/w/d) Business Development Manager (all genders) Business Development [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Dresden, Sachsen
[. .. ] contribute to the optimisation of testing processes and methods. Close collaboration with the development team will be essential as you document and track deviations, analyse test results, [...]
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[...] and ensure continuous quality assurance throughout the software lifecycle. We are looking for a candidate with a completed vocational training or university degree in computer science, software development, or a related discipline. Practical experience in automated testing with QF-Test or similar tools is highly desirable. Strong analytical thinking, a structured approach to work, and [. .. ] ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Associate Director Trial Master File
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] Cambridge, US; Gaithersburg, US; London, United Kingdom full time Job ID:9973 Associate Director Trial Master File (TMF) As Associate Director Trial Master File (TMF) , you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead TMF compliance, quality strategies, and operational excellence across Bio NTech-sponsored clinical trials, ensuring inspection readiness, regulatory compliance, and successful TMF archiving at trial completion. Your main responsibilities are: Provide strategic oversight and direction for TMF operations and governance across all phases of clinical trials Serve as the TMF SME and strategic advisor to [. .. ] primary TMF representative during audits and inspections, ensuring appropriate documentation access and participation in TMF-related interviews Collaborate closely with functions contributing to the TMF (e. g. Clinical Operations, Quality Assurance, Regulatory Affairs, etc. ) to ensure TMF integrity and consistent documentation practices Manage TMF vendor relationships and CRO oversight, including contract alignment, performance monitoring, and issue resolution Drive TMF training and knowledge management across the organization, ensuring that processes, roles, and systems are clearly understood and effectively implemented. Lead the [. .. ] business administration. Alternatively, more than 8 years of relevant experience in a regulated clinical development environment with demonstrable expertise in TMF strategy and oversight Minimum of 8 years in the pharmaceutical industry or clinical development roles, with at least 5 years of TMF-focused responsibilities Broad experience across TMF lifecycle management (start-up, maintenance, closeout, archiving) and a solid understanding of clinical trial processes Proven ability to lead TMF initiatives across cross-functional, global teams and provide strategic oversight of TMF [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Visp, Wallis
QA Responsible Person (RP) / Commercial
Quality Assurance Head Duration: Permanent contract (Onsite, Monday-Friday) Role and Responsibilities The Fachlich verantwortliche Person (Fv P) ensures all business is conducted in compliance [...]
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[...] with Swiss medicinal product law and company policies. By law, the RP is directly responsible for the technical supervision of the operation, safety, efficacy, and quality of medicines, [. .. ] compliance with Good Distribution Practice (GDP) . Collaborate with stakeholders across the company to understand processes outside of QA to determine the best path forward. Verify that manufacturers of imported pharmaceutical products hold a valid GMP manufacturing license. Ensure the traceability of all purchases and sales of pharmaceutical products and record the necessary information. Confirm that documentation proving the quality of traded batches of drug substance, intermediate drug product, and bulk product is complete. Independently decide on distribution stops and batch [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Head of GMP Manufacturing (all genders)
• Taufkirchen, Bayern
Führungs-/ Leitungspositionen
[. .. ] The Head of Manufacturing is responsible for the strategic leadership and operational daytoday management of all manufacturing activities, utilities and systems and in accordance with applicable regulatory [...]
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[...] requirements and internal quality standards at the site in Taufkirchen near Munich, Germany. The position holder will be part of the site leadership team. Responsibilities Lead and direct the GMP Manufacturing department overseeing drug product manufacturing, including process development, scaleup, technology transfer, formulation operations, and GMP production Provide technical leadership and mentorship to crossfunctional [. .. ] Maintain regulatory and GMP compliance (EU GMP, EMA, German regulatory bodies) in all operational and technical activities; ensure site readiness for audits and inspections Collaborate closely with Supply Chain, Quality Assurance, Regulatory Affairs, and Commercial teams to support product launch readiness and client commitments Qualifications Masters degree or Ph D in a scientific or engineering discipline Minimum of 10 years of experience in commercial or clinical manufacturing operations, including at least 5 years in a leadership role in a CDMO or (Bio) [. .. ] and written) to lead teams locally; Fluent in English Willingness for onsite presence in Munich, Germany Seniority level: Mid Senior level Employment type: Fulltime Job function: Production and Other Industries: Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr 73437511 [. .. ]
Job gestern bei Jobleads gefunden
• Schaffhausen
[. .. ] tomorrow and profoundly impact health for humanity. Learn more at https:/ / Are you interested in joining a team that is positively impacting and improving patients lives [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] by ensuring high quality in the manufacturing of our products? Apply today for this exciting opportunity The selected candidate will serve as a technical and automation subject matter expert (SME) , driving artwork automation initiatives, resolving complex technical artwork issues/ challenges, and partnering with cross-functional teams to deliver efficient, scalable solutions. This role [. .. ] communication. Qualifications Education: Bachelors degree required or advanced degree in Engineering, Graphic Design, or Supply Chain preferred. Experience Skills (Required) : At least 2 years of relevant experience in a Pharmaceutical/ regulated environment. Technical automation related experience in artwork, Regulatory Labeling or packaging fields. Experience in coordinating/ troubleshooting artwork, Regulatory Labeling packaging design (i. e. , variable data, barcode, automated technical template, brief content requirements) , Experience in coordinating/ creating packaging component technical templates, brief content instructions. 2+ years experience in [. .. ] Analytical Reasoning, Brand Research, Controls Compliance, Detail-Oriented, EHS Compliance, Good Manufacturing Practices (GMP) , Lean Supply Chain Management, Package and Labeling Regulations, Product Packaging Design, Proof Reading Software, Quality Assurance (QA) , Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy #J-18808-Ljbffr 73386719 [. .. ]
Job gestern bei Jobleads gefunden
Director Product Quality Management
• Schaffhausen
Führungs-/ Leitungspositionen
Job Function
Quality Job Sub Function Multi-Family Quality Job Category Professional All Job Posting Locations Schaffhausen, Switzerland Job Description About Innovative Medicine Our expertise in Innovative Medicine is informed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and inspired by patients, whose insights fuel our sciencebased advancements. Visionaries like you work on teams that save lives by developing the medicines [. .. ] you have the following essential requirements Requires a BA/ BS in Science/ Engineering. Masters degree in life science study or equivalent experience is preferrable, Minimum of 7 years experience previous Pharmaceutical Industry experience is required, with at least 7 years of GXP experience within clinical research and development and/or quality assurance. Up-to-date knowledge and in-depth understanding of relevant pharmaceutical legislation, legislation related to c GMP regulations (Eudralex, ICH, Ph. Eur. , USP, etc) at global, regional and national levels. Strong analytical thinking, decisionmaking and leadership skills. Excellent verbal and written communication skills to negotiate and communicate with customers and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Penzberg, Bayern
[. .. ] healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. Thats what makes us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Roche. In Roches Pharmaceutical Research and Early Development organization (p RED) , we make transformative medicines for patients to tackle some of the worlds toughest unmet healthcare needs. At p RED, we are united by our mission to transform science into medicine. Together, we create a culture defined by curiosity, responsibility and humility, where our talented [. .. ] TBLs into product specifications and cleaning validation procedures. You collaborate with crossfunctional teams to ensure control strategies are scientifically sound and compliant. You work closely with analytical chemists, formulation scientists, quality assurance, and regulatory affairs along with our Occupational Safety Teams. Your evaluations will be pivotal for the release of new batches from the manufacturing and quality functions You represent Roche as KOL in Industry Consortia and regulatory framework discussions groups You will advise and support project teams with regard to regulatory [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Quality Assurance Officer Belgium
[. .. ] having the security and additional career opportunities that working for a global CRO can bring? Our team says its the best of both worlds. Clin Choice is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] searching for a Quality Assurance Officer to work with one of our partner healthcare companies. This is a full-time (1FTE) position for 12months and we are open to considering candidates who are open to a temporary employment contract (FTC) or freelancers with their own company. The Quality Assurance Officer will support distribution activities including [. .. ] document retention system. Participate in Regulatory Affairs activities as needed. Education, Experience and Skills: Bachelors or Masters degree in a relevant scientific discipline. Prior experience within Quality Assurance within the pharmaceutical or healthcare environment. Basic knowledge of local regulations. Scientific knowledge. Administrative and project management skills. Ability to multitask and prioritise. Interpersonal and communication skills. Technical system skills, including word processing, spreadsheets, databases and online research. Fluent in English and French. Preferably with Dutch and German. The Application Process Once you [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Mainz, Germany full time Job ID:10586 We are seeking a strategic and visionary leader to oversee product development within a
Quality Management System (QMS) framework, driving innovation and ensuring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] adherence to regulatory standards and ultimately launching commercial products. As Senior Director Protein Modality Lead, you will provide leadership for all protein-based products (antibodies and antibody drug-conjugates) , ensuring phase-appropriate development and compliance with key regulations such as ICH [. .. ] Ensure alignment with risk management principles and regulatory guidelines, including ICH Q8, Q9, Q10 and others. Ensure Phase-Appropriate Development: Provide leadership for all protein-based products from a Quality Assurance perspective, ensuring phase-appropriate development while maintaining adherence to QMS and GMP standards. Lead Key Product Changes: Oversee and guide critical product changes related to regulatory compliance, quality, safety, efficacy, manufacturing sites, technology transfers, and commercial preparations and launches. Ensure alignment with global standards and successful execution of changes across [. .. ] challenges related to compliance and quality and product launches. Deep understanding of ICH guidelines (Q8, Q9, Q10) and their application in protein product development and lifecycle management. Longterm business and pharmaceutical understanding with the ability to anticipate and navigate strategic and tactical challenges in product development and commercialization. Proven ability to lead and develop teams, fostering a culture of collaboration and accountability while driving operational excellence. Exceptional analytical and problemsolving skills, with the ability to manage critical product deviations and regulatory [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Sr Director Ops BU OI DAP Warehouse
• Schaffhausen
Führungs-/ Leitungspositionen
[. .. ] the Site Leadership Team. Represent the Business Unit (BU) to internal and external customers and to governmental authorities. Operational Excellence Supply Ensure a reliable supply of products [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] that meets safety, quality and cost targets. Ensure flawless execution of new product introductions (NPI) and technology/ product transfer activities. Coordinate and supervise all new product introductions across the BU. Business Planning Financial Oversight Lead business planning within the BU. Maintain adherence to the BU budget. Provide oversight of ongoing operational costs and conduct [. .. ] BU to internal site, global organizations external stakeholders. Qualifications/ Requirements Education: Degree in Economics, Science, Engineering preferred (MBA, MSC, PHD) Experience: Minimum of 12 years of experience within ideally a pharmaceutical or GMP regulated Operations Department environment. Experience managing people and resources in an Operations department/ function, with at least 35 years of people management experience. Core Competencies Operations Department leadership experience within a Life Sciences or pharmaceutical environment. Experience of technology transfer and process optimization. Specific experience of manufacturing in [. .. ] Competitive Landscape Analysis, Critical Thinking, Good Manufacturing Practices (GMP) , Industry Analysis, Innovation, Leadership, Package and Labeling Regulations, Package Equipment, Package Management, Plant Operations, Product Packaging Design, Program Management, Quality Assurance (QA) , Safety Oriented, Standard Operating Procedure (SOP) , Sustainability, Sustainable Packaging #J-18808-Ljbffr 73261058 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Work-Life-Balance
[. .. ] improve internal processes or create new guidance Your profile: Masters degree OR Ph. D. in Biostatistics, Statistics, or a related field 6+ years of biostatistical experience in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] either a CRO, pharmaceutical, or biotech company Experience leading Phase II-III studies, including client facing responsibilities, timeline management, and resource oversight Experience working in a clinical research organization preferred Regulatory experience (supporting and the handling of regulatory requests, for example: NDA applications) Advanced ability to plan, supervise, implement, and monitor the statistical processes [. .. ] clinical studies Effective written and oral communication skills with demonstrated leadership ability Ability to prioritize with strong time management skills What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ] Programme, Life Works, offering 24-hour access to a global network of over 80, 000 independent specialized professionals who are there to support you and your familys well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. At ICON, inclusion belonging are fundamental to our culture and values. Were dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Director (m/f/x) Manufacturing
• Halle (Westf. ) , Nordrhein- Westfalen Halle;Kreisfreie Stadt Halle
Führungs-/ Leitungspositionen
Simtra Bio Pharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with
pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Bloomington, Indiana, US and Halle/ Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is c GMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring [. .. ] mindset in all areas of responsibility Ensure strict adherence to occupational safety standards, particularly in handling hazardous substances Represent the production function in crossfunctional collaboration with logistics, planning, controlling, quality assurance/ control, business management, and operational excellence teams What youll bring: Masters degree in natural sciences or engineering, preferably pharmacy, pharmaceutical engineering, food technology, biotechnology, or process engineering 510 years of proven success in operations management within a highperformance, fastpaced production environment Extensive experience in aseptic pharmaceutical manufacturing; background in cytostatic [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Quality Manager (m/f/x) Heidenheim a. d. Brenz/ Berlin/ remote
• Heidenheim an der Brenz, Baden- Württemberg
Quality Manager (m/f/x) Heidenheim a. d. Brenz/ Berlin/ remote QUALITY MANAGER (m/f/X) Heidenheim/Berlin/ remote You keep an eagle eye on quality details? GENERAL INFORMATION: Position: Quality Manager (m/f/x) Location: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] one of our offices in Heidenheim a. d. Brenz/ Berlin or remote (Germany) Starting: at the next possible date WHO WE ARE: THE FORCE builds companies on behalf of clients in the healthcare, pharmaceutical, and medical device sector, supports or manages customer projects of various kinds, and provides customers with qualified personnel to deal with bottlenecks or problems. We encourage work in a flexible surrounding and as a diverse group when it comes to gender, nationality, religion, and ways of working. This unique culture [. .. ] are looking for that certain something and will give it to you in return. WHAT WILL ALLOW YOU TO DIVE IN RIGHT AWAY: Your several years of experience in quality assurance in a manufacturing pharmaceutical company, ideally with close links to production and/or quality control, give wing to a good start. You are well acquainted with the standard processes of a GMP quality system, and have already been able to get your claws on practical experience in various processes. You [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Global Product Transfer Quality Engineer (Senior/ Staff)
• Zürich Zuerich
A global leader in medical technologies is seeking a Senior/ Staff
Quality Engineer in Zürich, Switzerland. You will support seamless product transfers, ensuring compliance with internal and external quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] standards. Responsibilities include reviewing validation documents, guiding quality strategies, and identifying risks during transfers. Candidates need a Bachelors degree and a minimum of 2 years experience in quality assurance within the medical or pharmaceutical fields, alongside proficiency in English and German. This position offers a flexible working model with 2 days on-site per week. #J-18808-Ljbffr 73212721 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Senior/ Staff Quality Engineer, Product Transfer (m/f/d)
• Zürich Zuerich
Homeoffice möglich
As a Senior/ Staff
Quality Engineer (m/f/d) in Strykers Product Transfer Quality Engineering function, you will play a key role in ensuring seamless product transfers, driving quality excellence, cost [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] optimization, and service improvements that directly benefit our customers. You will be an integral part of the QA Shared Services Product Transfer Team, collaborating [. .. ] FAI, inspection methods, and other key quality activities. What You Will Need Required Qualifications: Bachelors degree in Engineering, Sciences, or a related field. Minimum of 2 years experience in quality assurance and validation, ideally within the medical device or pharmaceutical industry. Strong knowledge of quality concepts, risk management tools (e. g. , FMEA, PPAP) , and regulatory standards (ISO 13485, FDA 21 CFR Part 820) . Proficiency in English German Preferred Qualifications: Experience in supplier quality and Quality Management Systems (QMS) . Hands-on experience with product transfers in regulated [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Oncology Portfolio Communications Public Affairs Leader
• Wien
Führungs-/ Leitungspositionen
[. .. ] key internal business groups and committees. Key Requirements Experience At least 10 years of experience in product and portfolio communications, public affairs, patient and/or a similar role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] within the pharmaceutical or healthcare industry. Proven success in launching innovative medicines in EMEA, media relations, digital strategy, congresses, and crisis management at a senior level. Experience in early market shaping is desirable. Strong leadership and excellent interpersonal skills, capable of operating at senior level with high strategic thinking, creating and maintaining relationships [. .. ] as needed. Preferred Skills Brand Reputation Management, Communications Measurement, Corporate Communications Management, Corporate Communications Strategy, Corporate Management, Cultural Competence, Developing Others, External Communication, Inclusive Leadership, Leadership, Media Relations, Organizational Knowledge, Quality Assurance (QA) , Relationship Building, Social Awareness, Stakeholder Engagement, Strategic Thinking, Team Management. Seniority level Not Applicable Employment type Full-time Job function Health Care Provider Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 73203222 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
ITOT Project Manager Infrastructure (m/f/d)
• Basel, Basel- Stadt
ITOT Project Manager Infrastructure (m/f/d) Project: For our customer a big
pharmaceutical company in Basel, we are looking for a ITOT Project Manager Infrastructure (m/f/d) Background: Are you passionate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] about Information (IT) and Automation Operational Technology (OT) and aspiring to make a meaningful impact? Are you curious to shape a digital manufacturing architecture, ready to advance competitiveness on the market? [. .. ] project lifecycle from initiation to closure. Ensure that projects are delivered on time, within budget, and in scope while adhering to strict Good Automated Manufacturing Practice, regulatory requirements and internal quality standards. Develop detailed project plans, schedules, resource allocations, and risk management strategies. Coordinate with internal cross-functional teams like Automation, Engineering, IT Security, Quality Assurance, Manufacturing and external vendors. Manage the selection, deployment and integration of hosting technologies essential for production facilities (e. g. , virtualized environments, cloud solutions, data centers) . Provide expertise and oversight regarding the proper selection, procurement, and usage of hardware components within a pharmaceutical production context (e. g. , industrial [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Quality Assurance pro Jahr?
Als Pharmaceutical Quality Assurance verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Quality Assurance Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 165 offene Stellenanzeigen für Pharmaceutical Quality Assurance Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Quality Assurance Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Pharmaceutical Quality Assurance Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Quality Assurance Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Quality Assurance Stellenangebote:
- GULP experts united (4 Jobs)
- Fresenius Kabi Deutschland GmbH (3 Jobs)
- Charles River (2 Jobs)
- RBW Consulting (2 Jobs)
- Arcadis (1 Job)
- IQVIA (1 Job)
In welchen Bundesländern werden die meisten Pharmaceutical Quality Assurance Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Quality Assurance Jobs werden derzeit in Bayern (26 Jobs), Baden-Württemberg (18 Jobs) und Nordrhein-Westfalen (17 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Quality Assurance Jobs?
Pharmaceutical Quality Assurance Jobs gehören zum Berufsfeld Qualitätswesen.
