26 Jobs für Pharmaceutical Quality Control Specialist
Stellenangebote Pharmaceutical Quality Control Specialist Jobs
Job am 14.11.2025 bei Neuvoo.com gefunden
Wickert Maschinenbau GmbH
• Rhineland- Palatinate Landau
[. .. ] one of the worlds leading suppliers of presses and press systems as well as services for the production of molded parts and related applications. Wickert presses are [...]
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[...] innovative with high quality and are used in various industries such as the pharmaceutical, automotive, aerospace and agricultural industries. We are a successful, family-run mechanical engineering company and have been an employer in the Southern Palatinate region since 1901. We are looking to strengthen our team at the earliest possible date Deputy IT Manager (m/f/d) Your area of responsibility Participation in [. .. ] implementation of the IT strategy Planning, managing and implementing IT projects, including resource and time planning Development and implementation of IT security concepts Support in the selection and implementation of specialist systems Monitoring and optimization of the existing IT infrastructure Creating and maintaining documentation on IT systems and projects Cost control and optimization of IT expenditure Organization and implementation of training courses for employees on the use of IT systems and applications and on IT security topics Close cooperation with other departments Interface between IT and external partners Contact person for all IT-related issues within the company Professional qualification Completed [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Sensient Technologies Europe GmbH
Specialist Quality Control
• Geesthacht
[. .. ] is a leading global manufacturer and marketer of colors, flavors, and extracts. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage [...]
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[...] systems, cosmetic and pharmaceutical systems, specialty colors, and other specialty and fine chemicals. The Companys customers include major international manufacturers representing most of the worlds best-known brands. The Companys high-performance products play a vital role in the manufacture of foods and beverages, cosmetic and pharmaceutical colors and coatings, and colors for agricultural uses, household cleaners and paper products. QA Specialist The QA Specialist is responsible for assisting in the development and maintenance of our certified ISO 9001:2015 quality management system, the GFSI recognized food safety management systems FSSC 22000 and IPEC standard compliant quality systems. This position will assure the compliance of our products with appropriate regulations, provide various data and risk assessments regarding our products and processes and serve as a resource to internal and external customers. [. .. ]
Job am 17.11.2025 bei JobMESH gefunden
Wickert Maschinenbau GmbH
Deputy IT Manager (m/f/d)
• Rheinland- Pfalz Landau
[. .. ] one of the worlds leading suppliers of presses and press systems as well as services for the production of molded parts and related applications. Wickert presses are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innovative with high quality and are used in various industries such as the pharmaceutical, automotive, aerospace and agricultural industries. We are a successful, family-run mechanical engineering company and have been an employer in the Southern Palatinate region since 1901. We are looking to strengthen our team at the earliest possible date Deputy IT Manager (m/f/d) Your area of responsibility Participation in [. .. ] implementation of the IT strategy Planning, managing and implementing IT projects, including resource and time planning Development and implementation of IT security concepts Support in the selection and implementation of specialist systems Monitoring and optimization of the existing IT infrastructure Creating and maintaining documentation on IT systems and projects Cost control and optimization of IT expenditure Organization and implementation of training courses for employees on the use of IT systems and applications and on IT security topics Close cooperation with other departments Interface between IT and external partners Contact person for all IT-related issues within the company Professional qualification Completed [. .. ]
Job am 14.11.2025 bei Mindmatch.ai gefunden
Novartis
QA Specialist Operations
• AT- 7 Kundl
Join to apply for the QA
Specialist Operations role at Novartis Join to apply for the QA Specialist Operations role at Novartis Summary QA Operations Specialist in the Raw Material [...]
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[...] Consumables Release Group. Summary QA Operations Specialist in the Raw Material Consumables Release Group. About The Role Major accountabilities: Release preparation (collection and completion of data, documents [. .. ] implementations (raw materials, consumables etc. ) , troubleshooting Project support Key performance indicators: deliver preparation on time, support raw material and consumables release and projects Minimum Requirements QC/ QA in pharmaceutical ind. / biotech with environmental monitoring Experience with GMP Procedures, Quality Assurance (QA) and Quality Control (QC) testing, Quality standards Technological Expertise and technological Intelligence Required skills: Dealing with ambiguity, able to learn continuously, collaborating across boundaries English and German language required Why Novartis? Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and [. .. ]
Job am 09.11.2025 bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
• AT- 7 Schaftenau
Job Description Summary We are seeking a
Quality Assurance professional to ensure Gx P compliance, product quality, and adherence to Novartis Manufacturing Manual and regulatory standards. Responsibilities include managing quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] systems, deviations, CAPAs, audits, training, and environmental monitoring. The role also supports product release, validation, and transfer projects while ensuring qualified facilities, business continuity, and compliance with HSE, DI, [. .. ] and manage quality agreements with third parties. Ensure business continuity and compliance with all corporate and local legal requirements. Essential Requirements: Microbiology or finalized apprenticeship in an area of the Pharmaceutical industry (e. g. chemical laboratory worker, chemical worker or related fields/ internal specific education (Modulausbildung) or equivalent) Fluent in German and intermediate proficiency in English Youll receive: In addition to a marketcompetitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development [. .. ] handbook to learn about all the ways well help you thrive personally and professionally: https:/ / Skills Desired Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance) , Quality Control (Qc) Testing, Quality Standards, Self Awareness, Technological Expertise, Technological Intelligence J-18808-Ljbffr 68862606 [. .. ]
Job am 09.11.2025 bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
Senior QA Operations Specialist (m/f/d)
• AT- 7 Schaftenau
Abgeschlossenes Studium
[. .. ] Schaftenau, Austria Treten Sie in eine Schlüsselrolle ein, in der Ihr Fachwissen sicherstellt, dass jeder Aspekt der pharmazeutischen Herstellung den höchsten Qualitäts- und Compliance-Standards entspricht. Als Senior [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] QA Operations Specialist (m/w/d) stehen Sie im Zentrum der Sicherstellung von Patientensicherheit und Produktqualität. Sie treiben die operative Integrität voran und unterstützen die Freigabe lebensverändernder Arzneimittel. Werden Sie Teil eines engagierten Teams bei Novartis, in dem Ihr Beitrag die gesamte Produktionskette beeinflusst und Ihr Qualitätsbewusstsein die Zukunft des Gesundheitswesens mitgestaltet. Step into a pivotal role where your expertise ensures that every aspect of pharmaceutical manufacturing meets the highest standards of quality and compliance. As a Senior QA Operations Specialist (m/f/d) , youll be at the heart of safeguarding patient safety and product excellence, driving operational integrity, and supporting the release of life-changing medicines. Join a collaborative team at Novartis, where your impact will be felt across the entire [. .. ] adherence to HSE guidelines across the site. Collaborate in internal and external audits and manage Quality Assurance Agreements with third parties. Review and approve specifications, test methods, and other quality control procedures. Act as the sites main contact for SAP and GLIMS activities, executing related actions and projects. Essential Requirements University degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or completed apprenticeship in a relevant pharmaceutical field. Professional experience in the pharmaceutical industry, ideally with at least 2 years in Quality Assurance. [. .. ]
Job am 03.11.2025 bei Mindmatch.ai gefunden
TSL
• AT- 9 Wien
Führungs-/ Leitungspositionen
TSL are a family-owned business, founded on inspirational ideas and a game changing approach to delivering turnkey capital projects for clients in Food,
Pharmaceutical, Logistics, Hi-Tech Manufacturing, Mega Sheds, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data Centres. Over the past 20 years, we are proud to have assembled talented teams of the brightest and most innovative people to work closely with our Specialist Designers, Project Managers, Commercial Managers, Construction and Technical Support Teams and ensure our clients are supported at every stage, from conception to construction and handover of their project. Following a period of rapid growth over the past 4 years, TSL have increased the group turnover to 1b. TSLs workforce is [. .. ] cascades the business objectives to drive performance throughout their business area. Conducts meaningful career development discussions and coaches potential in the team, in line with succession plans. Variations-assessment and control. Ensure review of Eo T requirements Contract-review and understand amendments and their implications Final accounts-all aspects-Client and supply chain Close out of the Projects to ensure seamless handover including PC Checklists and Building Control. Recognises the primary importance of Health and Safety and realises that, above all, the [. .. ] is money. Acts in the most time-conscious and efficient way when undertaking all tasks and keeps up with the pace of project programmes. Contributes to the development of the quality strategy. Implements, monitors and reviews quality performance against this strategy. Interprets legislation, policy and uses extensive specialist knowledge to develop strategy. Works with senior leaders to ensure alignment with legislation or policy to deliver best practice. Adapts services and systems accordingly. Operates as a subject matter expert in relevant area [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Quality Assurance Manager Product Quality Life Cycle Management (all genders)
• Leverkusen, Nordrhein- Westfalen
[. .. ] to join us. If youre hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, theres [...]
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[...] only one choice. Quality Assurance Manager Product Quality Life Cycle Management (all genders) Are you passionate about ensuring the highest quality standards in the pharmaceutical industry? We are looking for a dedicated Quality Assurance Manager Product Support (all genders) to join our team at the Supply Center Leverkusen. In this role, you will have the opportunity to make a significant impact on our products and processes. YOUR TASKS AND RESPONSIBILITIES You take responsibility as Quality [. .. ] Leverkusen You take responsibility for ensuring compliance with Pharmacopeias for the assigned pharmaceutical products You respond to Quality-related inquiries from internal and external partners, including customers, authorities, and various specialist functions You create and update local documents for Quality Control (QC) , such as study plans/ reports (e. g. method validation) , inspection plans, specifications, and test methods, in close cooperation with other experts You support GMP activities, including PQR processing, SOP creation, deviation management, and conducting root cause analyses to develop appropriate measures You represent the Quality capability pool [. .. ]
Job vor 7 Tagen 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 10 Tagen bei Jobleads gefunden
Quantity Surveyor
• Bayern
Quantity Surveyor Employment Type: Full-time Contract or Permanent (depending on candidate fit) About the Opportunity We are supporting a major
pharmaceutical construction and automation program in Germany and are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] seeking an experienced Quantity Surveyor to join the delivery team. This role will support commercial oversight across specialist packages including fire alarm systems, PAVA, and gas detection solutions within a highly regulated industrial environment. This position requires strong cost management, contract control, procurement oversight, and commercial reporting capability, alongside the ability to work collaboratively with suppliers, contractors, and engineering stakeholders. Key Responsibilities Lead commercial management for fire detection, PAVA, and gas detection system packages. Oversee cost planning, cost estimates, forecasting, and budget reporting throughout the project lifecycle. Prepare, negotiate, and manage contracts, [. .. ] teams, and external contractors to ensure alignment with project KPIs. Monitor onsite progress and validate contractor deliverables through measurement, valuation, and commercial audits. Ensure all activities comply with regulatory and quality requirements within the pharmaceutical construction environment. Provide regular commercial updates, reports, and cost analysis to senior management. Skills Experience Required Minimum 5 years experience in Quantity Surveying, ideally within MEP, designandbuild, or industrial construction projects. Experience working with fire safety, building automation, electrical, or specialist technology packages is highly advantageous. [. .. ]
Job vor 12 Tagen 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 14 Tagen bei Jobleads gefunden
Biomedical QC Lab Specialist GMP Empower Pro (Temp)
• Lengnau BE, Bern
A
pharmaceutical laboratory in Lengnau is seeking a Laboratory
Specialist Biomedical
Quality Control for a temporary position. The ideal candidate will have a Laboratory Technician diploma, at least [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2 years of experience in a chemical or biochemical lab, and mastery of Empower software. Responsibilities include analyzing products, maintaining laboratory equipment, and ensuring compliance with quality standards. Position starts in November 2025 and ends [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products and services. Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including [. .. ] Excellence Innovation Lead the continuous improvement and implementation of programming processes, workflows and tools, in close collaboration with biometry team leaders Establish and promote best practices for coding standards, version control, and automation across biometry teams Stay current on emerging technologies, industry standards, and innovations in programming and data science Business owner for Data Science platform (e. g. , POSIT) Strategic Cross-Function Partnership Collaborate closely with clinical science, data management and programming teams to identify and prioritize projects Advocate for [. .. ] has an effective combination of the following qualifications, skills and experiences: Masters degree in Computer Science, Data Science, Machine Learning, Applied Statistics, Mathematics, or related field 10+ years within a pharmaceutical company or CRO (required) . 3+ years in a supervisory or leadership role (preferred) Proven ability to program statistical analyses with deep knowledge of processes and procedures R Programming: Extensive R programming experience, including packages like dplyr and ggplot2 R Shiny: Handson expertise in building interactive dashboards and reports (bindings, [. .. ] level: Mid Senior level Employment type: Fulltime Job function: Information Technology Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Viatris by 2x Get notified about new Technical Solutions Specialist jobs in Allschwil, Basel-Country, Switzerland. #J-18808-Ljbffr 69796570 [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
LABORATORY SPECIALIST BIOMEDICAL QC
• Lengnau BE, Bern
We are actively looking for a Laboratory
Specialist Biomedical
Quality Control for a
pharmaceutical laboratory. LABORATORY SPECIALIST BIOMEDICAL QC-Temporary position Start date : November, 2025 End of date [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] : End of February, 2026 Location : Lengnau Perform analyses of finished products, samples in progress, raw materials, excipients, cleaning samples, validations and environmental monitoring according to established procedures. Ensure the maintenance and proper functioning [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
• München, Bayern
Principal Sourcing
Specialist Syneos Health Contract Specialist hybrid in Munich Syneos Health is a leading fully integrated biopharmaceutical solutions organization that accelerates customer success. It translates unique clinical, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affairs and commercial insights into outcomes to address modern market realities. The companys clinical development model places the customer and the patient at the [. .. ] for proposed contract and budget for site. Provides support in negotiating budget and contract with site via Site Contracts Service Centre and SSUL with Sponsor until resolution of issues. Performs quality control and arranges execution of CTAs as well as archival of documents into repositories and capture of metadata. Reviews contracts for completeness and accuracy, and ensures that corrections are appropriately made and documented. Provides supports to business development and represents site contracts/ Site Start Up (SSU) at internal or customer meetings. [. .. ] field, or equivalent combination of education and experience. Advanced degree preferred. High level of contracts management experience. Fluency in both German and English. Experience in a contract research organization or pharmaceutical industry essential and strong knowledge of the clinical development process and legal and contracting parameters. Customerfocused and ability to manage challenging priorities and to remain flexible and adaptable in stressful situations. Excellent understanding of clinical trial process across phases IIIV and ICH GCP. Good understanding of clinical protocols and associated [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Senior QA Operations Specialist (m/f/d)
• Schaftenau, Tirol
Abgeschlossenes Studium
[. .. ] Schaftenau, Austria Treten Sie in eine Schlüsselrolle ein, in der Ihr Fachwissen sicherstellt, dass jeder Aspekt der pharmazeutischen Herstellung den höchsten Qualitäts- und Compliance-Standards entspricht. Als Senior [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] QA Operations Specialist (m/w/d) stehen Sie im Zentrum der Sicherstellung von Patientensicherheit und Produktqualität. Sie treiben die operative Integrität voran und unterstützen die Freigabe lebensverändernder Arzneimittel. Werden Sie Teil eines engagierten Teams bei Novartis, in dem Ihr Beitrag die gesamte Produktionskette beeinflusst und Ihr Qualitätsbewusstsein die Zukunft des Gesundheitswesens mitgestaltet. Step into a pivotal role where your expertise ensures that every aspect of pharmaceutical manufacturing meets the highest standards of quality and compliance. As a Senior QA Operations Specialist (m/f/d) , youll be at the heart of safeguarding patient safety and product excellence, driving operational integrity, and supporting the release of life-changing medicines. Join a collaborative team at Novartis, where your impact will be felt across the entire [. .. ] adherence to HSE guidelines across the site. Collaborate in internal and external audits and manage Quality Assurance Agreements with third parties. Review and approve specifications, test methods, and other quality control procedures. Act as the sites main contact for SAP and GLIMS activities, executing related actions and projects. Essential Requirements University degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or completed apprenticeship in a relevant pharmaceutical field. Professional experience in the pharmaceutical industry, ideally with at least 2 years in Quality Assurance. [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
QA Senior Specialist (Mi Bi) 50-Schaftenau, Tirol
• Schaftenau, Tirol
Job Description Summary We are seeking a
Quality Assurance professional to ensure Gx P compliance, product quality, and adherence to Novartis Manufacturing Manual and regulatory standards. Responsibilities include managing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] quality systems, deviations, CAPAs, audits, training, and environmental monitoring. The role also supports product release, validation, and transfer projects while ensuring qualified facilities, business continuity, and compliance with HSE, DI, [. .. ] and manage quality agreements with third parties. Ensure business continuity and compliance with all corporate and local legal requirements. Essential Requirements: Microbiology or finalized apprenticeship in an area of the Pharmaceutical industry (e. g. chemical laboratory worker, chemical worker or related fields/ internal specific education (Modulausbildung) or equivalent) Fluent in German and intermediate proficiency in English Youll receive: In addition to a marketcompetitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development [. .. ] handbook to learn about all the ways well help you thrive personally and professionally: https:/ / Skills Desired Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance) , Quality Control (Qc) Testing, Quality Standards, Self Awareness, Technological Expertise, Technological Intelligence #J-18808-Ljbffr 68926050 [. .. ]
Job am 13.10.2025 bei Jobleads gefunden
Project Director
• Wien
Führungs-/ Leitungspositionen
TSL are a family-owned business, founded on inspirational ideas and a game changing approach to delivering turnkey capital projects for clients in Food,
Pharmaceutical, Logistics, Hi-Tech Manufacturing, Mega Sheds, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Data Centres. Over the past 20 years, we are proud to have assembled talented teams of the brightest and most innovative people to work closely with our Specialist Designers, Project Managers, Commercial Managers, Construction and Technical Support Teams and ensure our clients are supported at every stage, from conception to construction and handover of their project. Following a period of rapid growth over the past 4 years, TSL have increased the group turnover to 1b. TSLs workforce is [. .. ] cascades the business objectives to drive performance throughout their business area. Conducts meaningful career development discussions and coaches potential in the team, in line with succession plans. Variations-assessment and control. Ensure review of Eo T requirements Contract-review and understand amendments and their implications Final accounts-all aspects-Client and supply chain Close out of the Projects to ensure seamless handover including PC Checklists and Building Control. Recognises the primary importance of Health and Safety and realises that, above all, the [. .. ] is money. Acts in the most time-conscious and efficient way when undertaking all tasks and keeps up with the pace of project programmes. Contributes to the development of the quality strategy. Implements, monitors and reviews quality performance against this strategy. Interprets legislation, policy and uses extensive specialist knowledge to develop strategy. Works with senior leaders to ensure alignment with legislation or policy to deliver best practice. Adapts services and systems accordingly. Operates as a subject matter expert in relevant area [. .. ]
Job am 06.10.2025 bei Jobleads gefunden
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
WICKERT Maschinenbau GmbH
Deputy IT Manager (m/f/d) - For German Resident Only
• Landau
[. .. ] one of the worlds leading suppliers of presses and press systems as well as services for the production of molded parts and related applications. Wickert presses are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innovative with high quality and are used in various industries such as the pharmaceutical, automotive, aerospace and agricultural industries. We are a successful, family-run mechanical engineering company and have been an employer in the Southern Palatinate region since 1901. We are looking to strengthen our team at the earliest possible date Deputy IT Manager (m/f/d) Your area of responsibility Participation in [. .. ] implementation of the IT strategy Planning, managing and implementing IT projects, including resource and time planning Development and implementation of IT security concepts Support in the selection and implementation of specialist systems Monitoring and optimization of the existing IT infrastructure Creating and maintaining documentation on IT systems and projects Cost control and optimization of IT expenditure Organization and implementation of training courses for employees on the use of IT systems and applications and on IT security topics Close cooperation with other departments Interface between IT and external partners Contact person for all IT-related issues within the company Professional qualification Completed [. .. ]
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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 26 offene Stellenanzeigen für Pharmaceutical Quality Control Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Quality Control Specialist Jobs?
Aktuell suchen 7 Unternehmen nach Bewerbern für Pharmaceutical Quality Control Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Quality Control Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Quality Control Specialist Stellenangebote:
- Wickert Maschinenbau GmbH (3 Jobs)
- Healthcare Businesswomens Association (2 Jobs)
- Sensient Technologies Europe GmbH (1 Job)
- Novartis (1 Job)
- TSL (1 Job)
- WICKERT Maschinenbau GmbH (1 Job)
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 (5 Jobs), Nordrhein-Westfalen (3 Jobs) und Sachsen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Quality Control Specialist Jobs?
Pharmaceutical Quality Control Specialist Jobs gehören zum Berufsfeld Qualitätswesen.
