17 Jobs für Pharmaceutical Quality Control Specialist
Stellenangebote Pharmaceutical Quality Control Specialist Jobs
Job gestern bei Jobleads gefunden
• Pfaffenhofen an der Ilm, Bayern
Application
Specialist (m/f/d) / SAP/ MESKey User (w/f/d) Pharma Production Join to apply for the Application Specialist (m/f/d) / SAP/ MESKey User (w/f/d) Pharma Production role at Daiichi Sankyo Europe [...]
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[...] Gmb H. Responsibilities First Level Support for SAP (S/ 4HANA, EWM, MM, PP, SD) and [. .. ] Assisting with the decommissioning, creation, modification and deletion of material numbers and masterdata processes in SAP. Conducting and correcting movement data in SAP S/ 4HANA and EWM to ensure inventorydata quality (e. g. , losses, transfers, inventory differences) . Preparing and analysing key metrics and reports to support production control and process improvement. Actively contributing to the further development of SAP/ MES processes, particularly with a view to automation and digitisation. Creating work instructions, training materials and conducting training in a GM Pregulated environment. Processing error messages, change requests and change proposals in compliance with regulatory requirements (GMP, ISO, DIN) [. .. ] (Excel, Power Point, Word) ; ideally experience with dataanalysis tools (e. g. , Power BI) . Employment Details Seniority level: Entry level Employment type: Fulltime Job function: Information Technology Industry: Pharmaceutical Manufacturing #J-18808-Ljbffr 73437456 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• München, Bayern
Job Description An unserem Standort in München suchen wir zum nächstmöglichen Zeitpunkt einen
Specialist In-Market
Quality (m/w/d) in Vollzeit unbefristet. Der Fokus unserer In-Market Quality Abteilung liegt in der Aufrechterhaltung [...]
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[...] unseres Qualitätsmanagementsystems unter Einhaltung der Forderungen der Good Distribution Practice (GDP) - Guideline. Nur so können wir die hohen Qualitätsstandards unserer Arzneimittel während ihres Vertriebs sicherstellen und damit die Patientensicherheit gewährleisten. Ziel dieser [. .. ] 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, 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 as Merck Sharp [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Specialist In-Market Quality (m/w/d)
• München, Bayern
Specialist In-Market
Quality (m/w/d) page is loaded # # Specialist In-Market Quality (m/w/d) remote type: Hybridlocations: DEU-Bavaria-Munichtime type: Full timeposted on: Posted Todaytime left to apply: End Date: January 9, [...]
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[...] 2026 (20 days left to apply) job requisition id: R378333Job Description An unserem Standort in München [. .. ] 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, 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. , Rahway, NJ, [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• 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: one [...]
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[...] 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 [. .. ] 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 have a keen eye on the requirements of German and European laws and standards in [. .. ] up knowledge, and strive to constantly improve your skills. WHAT WILL MAKE YOU FIT THE BILL EVEN MORE: You have broadened your horizons through further practical experience, or are a specialist in topics such as the introduction of electronic systems. Experience in manufacturing processes of various pharmaceuticals such as nonsterile, solid and liquid dosage forms, parenterals, biologics or radiopharmaceuticals is an additional feather in your cap. You have already successfully spread your wings in project management. Your commercial mindset is more [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Köln, Nordrhein- Westfalen Koeln
Executive
Specialist Recruitment Randstad Denmark 2care4 Germany We are looking for an experienced Responsible Person and Narcotic Officer to be the on-site authority for
quality and compliance at 2care4s Cologne-Ossendorf [...]
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[...] location. The role covers legal compliance for two entities 2care4 Gmb H and Allomedic Gmb H and supports 2care4s ambitious growth strategy in Germany by transforming quality systems from manual to digital and scalable processes. Main responsibilities Ensuring compliance with GDP guidelines and handling narcotic trade. Contributing to achieving the companys business objectives. Creation and maintenance of Standard Operating Procedures (SOPs) and Technical Agreements. Deviation, Change Control, and CAPA management, as well as handling complaints/ claims. Organization, coordination, and documentation of national and cross-border narcotics trade. Implementation of GDP guidelines, conducting internal and external quality audits, and GDP selfinspections. Planning and implementation of qualification and validation measures, including temperature monitoring. Preparation and execution of internal courses [. .. ] position, please contact principal consultant Kasper Kjrgaard on +45 61 95 92 51. All inquiries will be handled confidentially. About 2care4 Founded in 2005 in Esbjerg, 2care4 is an international pharmaceutical company that has experienced rapid growth, with approximately 360 employees across Europe. The core business is the parallel import of medicine, involving purchasing original medicine in EU/ EEA countries and repackaging it for local markets. The companys purpose is to create savings for society through dedication by increasing competition. As [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Wien
[. .. ] technologies. Our products help clarifying allergies in a single step for humans and animals alike. Allergies are diagnosed in a highly specific manner so that patients receive [...]
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[...] help by their specialist in no time. We increase quality of life, enable personalized treatment, advance research and relieve our health system. Location: Vienna, Austria Benefits Annual pass for Viennas public transport and Sodexo vouchers Collaboration with people who care about human and veterinary patients alike An environment where you feel empowered to ask questions, make requests and offer ideas [. .. ] Motivation to grow in exciting projects within a team and the ability to work independently A solid foundation in statistical analysis and algorithms Familiarity with cloud, orchestration, containerization, and versioning control methodologies Compensation We offer a payment in line with the collective agreement (KV Handwerk und Gewerbe) based on a parttime position. Your actual salary depends on your previous experience and qualifications. Seniority level Associate Employment type Fulltime Job function Information Technology, Science, and Engineering Industries Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing Ready to become part of the MADx team? Then apply with your CV at our website #J-18808-Ljbffr 73146794 [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Laboratory
Specialist (Paid Consultancy Opportunity) Company-RONIN International is an independent B2B market research company specialising in business, healthcare and tech studies. We are part of the Rippleffect Group (formerly [...]
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[...] Fat Media Group) and are Company of The Market Research (MRS) , Corporate Members of ESOMAR, Members of the Insights Association and Council Members of The Interviewer Quality Control Scheme (IQCS) . About-We are recruiting for laboratory decision makers for a paid consultancy session on an online research study. Qualifications: Germany-based Need to responsibility for flow cytometer purchasing decisions The purpose of this study is to understand the purchase pattern and usage of flow cytometry among Decision [. .. ] lasting for 30 minutes. Compensation package-EUR 85 for 30 minutes online Seniority level Mid-Senior level Employment type Temporary Job function Science, Quality Assurance, and Health Care Provider Industries Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care #J-18808-Ljbffr 72999705 [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Heidelberg, Baden- Württemberg
[. .. ] experienced within risk management, overseeing external production, and roll out of drug-device combination products? If so, now is your chance to join Ascendis Pharma as our new [...]
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[...] Senior Device Specialist. Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in patients lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative Trans Con technology platform to fulfill our mission of developing new therapies that demonstrate bestinclass potential to address unmet [. .. ] and suppliers to maintain and roll out our products globally. Qualifications and Skills: You hold a relevant technical degree and five to eight years of experience within medical device or pharmaceutical industry. you have: Formally trained and proven track record within Medical Device Risk Management (ISO14971:2019) . You have reviewed information from production and postproduction activities, initiated relevant CAPA and updated RMF accordingly. Experience with Post Market Surveillance submissions is a plus. (Be specific about your experience in your application. ) Experienced within injection devices (ISO11608-1 2:2022) , design control and drug-device combination product legislation (ISO13485, MDR, 21 CFR Part 820 and 4) . Experience with change control, deviation and CAPA management, control setup and product quality complaints. Experience with maintenance of Device History File, registrations of device and drug-device combination products as well as oversight on supplier services and projects. You are a strong team player, analytical, and have a cando attitude. You possess an entrepreneurial mindset and can thrive in an informal, open environment [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
• Bern
[. .. ] applicants Direct message the job poster from CTC Resourcing Solutions Senior Recruitment Consultant at CTC Resourcing Solutions Senior Documentation Engineer-Primary Packaging Medical Devices-6763 ADA Our client is [...]
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[...] a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, immunological diseases, enzyme deficiency diseases, and other rare diseases. We are seeking a highly skilled Senior Documentation Engineer for their Primary Packaging Medical Devices unit. It is an initial 12month [. .. ] materials, medical devices, and Combination Product for legacy products. You will provide scientific support to maintain the design of the existing commercially released Combination Products. Coordinate cross-functionally with Regulatory, Quality Assurance, Production, Manufacturing, and Supply Chain to provide post launch support, including design and supplier-related changes, product complaints, root cause analysis and other compliance projects. You will be responsible for executing projects within the agreed time, quality and cost constraints, resulting in stateoftheart drug delivery devices. Develop high-level [. .. ] responsibility. You will be required to apply your knowledge of the regulatory landscape to ensure standard compliant designs, working to Quality Management Systems such as ISO 13485, and 21CFR820 Design Control, risk management to ISO14971, EU MDR requirements. Main Responsibilities Assure that design control is performed according to current scientific rational, regulatory/ internal guidelines, legal requirements and quality standards. Ensuring data integrity and scientific consistency in all verification testing. Promote data analyses using advanced statistical techniques and communicate results to a [. .. ] and drug delivery. Experience with Design Control Documentation, Risk Management and SOP writing. Fluent in English, German fluency an advantage. Seniority level Mid Senior level Employment type Contract Job function Pharmaceutical Manufacturing #J-18808-Ljbffr 70789662 [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• Basel, Basel- Stadt
[. .. ] The Particle Design Team at Roche is dedicated to developing robust and efficient processes for small molecule drug substances. We work at the intersection of chemical engineering, [...]
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[...] physical chemistry, and pharmaceutical science to define and control the final solid forms and solid-state attributes required for optimal drug product quality and manufacturing. We are seeking a highly motivated and skilled Senior Crystallization Specialist/ Senior Particle Engineer to join our team. This role is crucial for developing crystallization and isolation processes, applying particle engineering technologies, and ensuring drug substances meet defined quality attributes for robust drug product manufacturing. The ideal candidate will have a strong background in crystallization fundamentals and process development, excellent interpersonal [. .. ]
Job am 06.10.2025 bei Jobleads gefunden
Editorial/ Quality Control (QA) Specialist
• München, Bayern
Editorial/
Quality Control (QA)
Specialist We are seeking a meticulous Editorial/ Quality Control (QA) Specialist to be the final eye for accuracy, clarity, and brand consistency across our client [...]
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[...] deliverables. You will play a pivotal role in ensuring that regulatory, clinical, and commercial outputs meet the highest scientific, editorial, and formatting standards. This role is [. .. ] eye for detail and commitment to editorial excellence will directly impact the credibility and success of client deliverables. Seniority Level Mid Senior level Employment Type Fulltime Job Function Production Industries Pharmaceutical Manufacturing and Business Consulting and Services #J-18808-Ljbffr 64827162 [. .. ]
Job am 03.10.2025 bei Jobleads gefunden
PLC software developer (m/f/d) 1
• Niederdorf, Bayern
Responsibilities Creation of the complete machine software in the area of HMI,
control and drive technology for our packaging machine Part of a project team and responsible for the [...]
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[...] program preparation, commissioning, acceptance and data backup of our packaging machines Clarification of project-specific requirements of the control functions within the project team Creation of concepts, specifications and solutions for interfaces and functions of software modules in close coordination with specialist colleagues, application technology, mechanical and electrical engineering Implementation of control software for the modular system and for order-specific solutions Performance of quality assurance tests and participation in the development of system and validation tests Supporting the project management in project planning and tracking progress of projects Supporting the project and sales management regarding technical questions Requirements Completed studies in the field of electrical engineering, automation technology, mechatronics or comparable training (technician specializing [. .. ] trends in the development of intelligent, future-oriented machine technology for over 45 years, from film wrapping and case packaging to palletizing. Our customers include well-known companies in the pharmaceutical and consumer goods industries. As a globally operating family business with international sales and service locations, we are in direct dialog with our customers. Over 800 employees worldwide are committed to our success. Have we aroused your interest? If so, we look forward to receiving your online application Your contact: [. .. ]
Job am 03.10.2025 bei Jobleads gefunden
Senior Service Now Compliance Validation Lead (Freelancer)
• Bonn, Nordrhein- Westfalen
Führungs-/ Leitungspositionen Freiberuflich
To support our global IT initiatives within a regulated
pharmaceutical environment we are looking for an experienced IT Service Now Compliance Validation Lead. In this role you will be [...]
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[...] responsible for ensuring that the Service Now platform is qualified, validated and maintained in a Gx Pcompliant manner while acting as the bridge between IT Quality Assurance and business stakeholders. Frame Conditions Location : Remote Contract type : Freelance (full-time assignment) Industry : Pharmaceutical/ Life Sciences Duration : 12 months Note : Only candidates located within the EU can be considered. Tasks Develop and execute the compliance and validation strategy for the Service Now platform [. .. ] Plans Risk Assessments URS IQ/ OQ/ PQ Traceability Matrices) . Define and enforce Gx P controls audit trails and data integrity principles (ALCOA) . Support system reviews revalidation activities and change control processes. Act as IT lead during audits and regulatory inspections. Collaborate closely with QA IT Security Business Process Owners and Service Now developers. Provide training and ensure SOPs and Work Instructions are up to date. Requirements 5 years of IT compliance/ validation experience in the pharmaceutical or life sciences industry. [. .. ] stakeholder management skills. Experience with validated Saa S platforms and vendor qualification processes is a plus. Fluency in English required. Preferred Certifications (nice-to-have) Service Now Certified System Administrator/ Implementation Specialist GAMP 5 or CSV-related certifications ITIL Foundation Certification Project Management Certification (PMP or PRINCE2) Employment Type : Full Time Experience : years Vacancy : 1 #J-18808-Ljbffr 64372232 [. .. ]
Job am 29.09.2025 bei Jobleads gefunden
Senior Specialist, Supplier Quality
• Eschweiler, Nordrhein- Westfalen
[. .. ] live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary In this role you will be responsible [...]
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[...] for performing Supplier Quality activities associated with external suppliers. This role performs activities to ensure West suppliers maintain compliance with Wests procedures and policies. You will interface with R D, Sourcing, Design Quality, Regulatory and Operations Quality to drive improved supplier quality performance. Essential Duties and Responsibilities Establish and successfully execute supplier management plans [. .. ] Education Bachelors Degree in Science or equivalent experience required Masters Degree in Science or equivalent experience preferred Work Experience Minimum 5 years of quality related experience with preferred experience in pharmaceutical and/or medical device industry Experience working with suppliers and supplier engagement activities Preferred Knowledge, Skills and Abilities Knowledge of sterilization process is preferred Knowledge of c GMP, c GDP, relevant ISO standards, medical device requirements and other international regulations Familiarity with Master Control, SAP and working knowledge of statistical data analysis Fluent in English Thorough understanding of validation activities and risk management principles and techniques Strong problem-solving and critical thinking skills Negotiation skills and collaborating with suppliers Ability to work under high volume production and fast changing environment Willingness to work in [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
Senior Specialist, Supplier Quality
• Eschweiler, Nordrhein- Westfalen
Select how often (in days) to receive an alert: Job Overview Requisition ID: 71354 Date: Sep 25, 2025 Location: Eschweiler, North Rhine-Westphalia, DE Department:
Quality Description: This is a [...]
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[...] hybrid position (3 days per week) working in our office at Eschweiler, Germany. Candidates applying must be residing within a 50-mile commutable distance to the job location. At West, were a dedicated team that is connected by a purpose to improve patient lives that has [. .. ] Education Bachelors Degree in Science or equivalent experience required Masters Degree in Science or equivalent experience preferred Work Experience Minimum 5 years of quality related experience with preferred experience in pharmaceutical and/or medical device industry Experience working with suppliers and supplier engagement activities Preferred Knowledge, Skills and Abilities Knowledge of sterilization process is preferred Knowledge of c GMP, c GDP, relevant ISO standards, medical device requirements and other international regulations Familiarity with Master Control, SAP and working knowledge of statistical data analysis Fluent in English Thorough understanding of validation activities and risk management principles and techniques Strong problem-solving and critical thinking skills Negotiation skills and collaborating with suppliers Ability to work under high volume production and fast changing environment Willingness to work in [. .. ]
Job am 15.09.2025 bei Jobleads gefunden
Lab IT Specialist (f/m/d)
• München, Bayern
Overview Join to apply for the Lab IT
Specialist (f/m/d) role at Coriolis Pharma. Purpose of your Job As a Lab IT Specialist, you will ensure that Coriolis laboratory [...]
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[...] IT systems run smoothly, reliably, and in compliance with all quality standards. This role is central to maintaining seamless lab IT workflows, managing infrastructure, performing on-site technical support, and overseeing system setup, maintenance, and qualification. Youll act as the key link between scientists, lab technicians, IT infrastructure colleagues, and software vendors, helping to optimize processes and keep laboratory operations running [. .. ] related issues Good understanding of IT infrastructure components and experience with computer system validation Ability to troubleshoot software and hardware issues in laboratory systems Familiarity with IT security, user access control, audit trail handling and data integrity requirements Experience with LINUX and Windows operating systems as well as database setup and management Strong communication and training skills, especially with non-technical lab users Fluency in German and English (both written and spoken) High sense of responsibility, accuracy, and compliance awareness Team-[. .. ] problem-solving, attention to detail, and excellent organizational skills Availability to work on site in Martinsried Seniority level Mid-Senior level Employment type Full-time Job function Information Technology Industries: Pharmaceutical Manufacturing #J-18808-Ljbffr 62070409 [. .. ]
Job am 07.09.2025 bei Jobleads gefunden
Director of CMC
Führungs-/ Leitungspositionen
Director/ Senior Director, CMC role description and overview is provided below. Senior Business Manager-Global CDMO
Specialist Overview Senior-level position leading all CMC responsibilities in Germany within a cutting-edge CDMO [...]
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[...] company specializing in Small and Large Molecules and advanced therapies. This role offers the opportunity to contribute to the development of the CMC team across three verticals and participate in groundbreaking medical innovations. Responsibilities Lead [. .. ] Process Development department, managing a team of scientists and technical experts. Oversee method development, qualification, validation, and transfer for raw materials, intermediates, APIs, and finished products. Collaborate cross-functionally with Quality Control, Regulatory Affairs, and Manufacturing teams. Ensure analytical strategies align with ICH guidelines, EU GMP, and client-specific requirements. Drive technology innovation, including implementation of advanced analytical platforms (e. g. , LC-MS, q PCR, spectroscopy) . Serve as the technical lead during client audits, regulatory inspections, and project meetings. Develop and [. .. ] submissions, and CTD sections for INd/IMPD filings. Stay abreast of industry trends, regulatory changes, and emerging technologies in analytical sciences. Requirements Ph D or MSc in Analytical Chemistry, Biochemistry, or Pharmaceutical Sciences 10+ years in analytical development, ideally within a CDMO or pharma/ biotech setting 4+ years in process development, ideally within a CDMO setting Proven leadership and team-building experience Deep expertise in GMP, ICH guidelines, and regulatory expectations Strong communication skills in German and English Desired Competencies Hands-on [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Quality Control Specialist pro Jahr?
Als Pharmaceutical Quality Control Specialist verdient man zwischen EUR 45.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Quality Control Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 17 offene Stellenanzeigen für Pharmaceutical Quality Control Specialist Jobs.
In welchen Bundesländern werden die meisten Pharmaceutical Quality Control Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Quality Control Specialist Jobs werden derzeit in Bayern (7 Jobs), Nordrhein-Westfalen (4 Jobs) und Baden-Württemberg (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Quality Control Specialist Jobs?
Pharmaceutical Quality Control Specialist Jobs gehören zum Berufsfeld Qualitätswesen.
