21 Jobs für Pharmaceutical Quality Control Specialist
Stellenangebote Pharmaceutical Quality Control Specialist Jobs
Job vor 8 Tagen bei Mindmatch.ai gefunden
CTC Resourcing Solutions
• AT- 2 Lavamünd
Quality Assurance Associate 6949 Unser Kunde ist ein spezialisierter Hersteller von Biotherapeutika mit über einem Jahrhundert Erfahrung in der Behandlung verschiedener Krankheiten weltweit. Das Unternehmen engagiert sich für Patienten mit [...]
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[...] Gerinnungsstörungen, immunologischen Erkrankungen, Enzymmangelkrankheiten und anderen seltenen Krankheiten. Wir suchen einen hochqualifizierten Mitarbeiter für die Qualitätssicherung für eine 1-jährige befristete [. .. ] bei sich ändernden Sachverhalten. Ein hohes Mass an Selbständigkeit und Eigeninitiative. Muttersprache Deutsch und sehr gute Kenntnisse in Englisch, schriftlich und mündlich. Quality Assurance Associate 6949 Our client is 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 Quality Assurance Associate for an initial 1 year contract position at our clients headquarters in [. .. ] Support and consulting in the area of aseptic manufacturing and microbiological laboratories (no performance of activities within manufacturing or the laboratory) Review and ensure compliance with GMP requirements in production Control, review, and documentation of work steps, review of processes in aseptic production. Participation in the training and (re) qualification of aseptic production employees Support for deviations in the area of aseptic filling: Conducting initial assessments Supporting the definition of the investigation strategy, including the evaluation of technical assessments within the [. .. ] documents Qualifications Experience: Relevant working/ residency permit or Swiss/ EU-Citizenship required Educational Background: Degree in a scientific field (preferably Pharmacy, Chemistry, or Biology) . Experience: Ideally, experience within a pharmaceutical company and GMP environment. 1-2 years of experience in Quality Assurance/ Quality Control 1-2 years of experience with QMS Strong enthusiasm, analytical thinking, and effective communication skills. Precise and reliable work approach with the ability to prioritize effectively. Flexibility and ability to work independently as well as in [. .. ]
Job am 22.04.2026 bei Mindmatch.ai gefunden
Octapharma Austria
Quality Auditor Regulatory Compliance Specialist (m/f/d) - Group Quality Plasma
• AT- 9 Wien
Job-ID: 62409 Location: Wien, AUT Job Level: Professionals Category:
Quality Employment Type: Permanent position Become part of a vital chain and contribute to our common goal of making peoples lives [...]
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[...] better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privatelyowned company, where the warmth of family meets the scale of a global organisation. Quality Auditor Regulatory Compliance Specialist You are responsible for ensuring the quality and regulatory compliance of Octapharmas plasma suppliers on a corporate level. The role combines supplier qualification, audit activities, and regulatory tasks, with a strong focus on data accuracy, compliance, and structured stakeholder interaction. Main Tasks and Responsibilities Ensure quality and regulatory compliance of plasma suppliers on a global level Manage change control, deviations, and qualityrelated contracts Conduct external supplier audits, participate in customer/ internal audits at our facility Analyze and trend supplierrelated quality data Create, review, and train on SOPs and related procedures Qualify plasma suppliers and service providers (e. g. testing laboratories, logistics partners) Monitor and ensure continuous supplier compliance throughout [. .. ] PMF approvals Collaborate with internal and external stakeholders, including suppliers, health authorities, and crossfunctional departments Expertise and Ideal Skill Set Degree in Life Sciences (e. g. , Biology, Chemistry, or Pharmaceutical Sciences) Professional experience in Quality Assurance within the pharmaceutical industry Proficient knowledge of GMP, EU and FDA guidelines Experience with quality management systems, particularly Veeva Auditor certification, audit experience, basic quality auditor or ISO course is a strong advantage Structured, reliable, and independent working style, combined with strong communication skills [. .. ]
Job am 14.03.2026 bei Mindmatch.ai gefunden
CTC Resourcing Solutions
• AT- 2 Lavamünd
Quality Assurance Associate 6900 Unser Kunde ist ein spezialisierter Hersteller von Biotherapeutika mit über einem Jahrhundert Erfahrung in der Behandlung verschiedener Krankheiten weltweit. Das Unternehmen engagiert sich für Patienten mit [...]
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[...] Gerinnungsstörungen, immunologischen Erkrankungen, Enzymmangelkrankheiten und anderen seltenen Krankheiten. Wir suchen einen hochqualifizierten Mitarbeiter für die Qualitätssicherung für eine 6-monatige befristete [. .. ] bei sich ändernden Sachverhalten. Ein hohes Mass an Selbständigkeit und Eigeninitiative. Muttersprache Deutsch und sehr gute Kenntnisse in Englisch, schriftlich und mündlich. Quality Assurance Associate 6900 Our client is 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 Quality Assurance Associate for an initial 6-month contract position at our clients headquarters in [. .. ] Support and consulting in the area of aseptic manufacturing and microbiological laboratories (no performance of activities within manufacturing or the laboratory) Review and ensure compliance with GMP requirements in production Control, review, and documentation of work steps, review of processes in aseptic production. Participation in the training and (re) qualification of aseptic production employees Support for deviations in the area of aseptic filling: Conducting initial assessments Supporting the definition of the investigation strategy, including the evaluation of technical assessments within the [. .. ] Experience: Relevant working/ residency permit or Swiss/ EU-Citizenship required Educational Background : Degree in a scientific field (preferably Pharmacy, Chemistry, or Biology) . Experience : Ideally, experience within a pharmaceutical company and GMP environment. 1-2 years of experience in Quality Assurance/ Quality Control 1-2 years of experience with QMS Strong enthusiasm, analytical thinking, and effective communication skills. Precise and reliable work approach with the ability to prioritize effectively. Flexibility and ability to work independently as well as in [. .. ]
Job vor 4 Tagen bei Jooble gefunden
DNHK
Accounting Specialist
• Regierungsbezirk Düsseldorf; Westfalen Duesseldorf
Overview Lab Connect improves lives by partnering with
pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are an [...]
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[...] independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex [. .. ] an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. Job Summary The Account Specialist is responsible for supporting monthly, quarterly, and annual financial and accounting activities, including General Ledger support (balance sheet and P L) , Accounts Payable (AP) , Accounts Receivable (AR) , and VAT declarations for Lab Connect. This role supports AP and AR processes by identifying and resolving alignment issues and [. .. ] completeness, and compliance with internal controls and reporting standards Assist with the preparation of financial statements and internal management reports Perform intercompany reconciliations and support resolution of variances Support inventory control activities, including cycle counts, pricing validation, and process documentation Coordinate VAT filing processes in partnership with external advisors and the Finance Director Assist the Finance Director with data preparation and support related to corporate income tax filings Support analysis of business operations, costs, and revenues to assist with forecasting and [. .. ] trials through innovation, agility, and collaboration. We believe that our people are our greatest asset, and we are committed to fostering a workplace that reflects our core values: People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always. Lab Connect is an Equal Opportunity Employer. We celebrate diversity and are dedicated to creating an inclusive environment for all employees. We do not discriminate based on race, color, religion, sex (including pregnancy, gender identity, and sexual orientation) , creed, national origin, [. .. ]
Job vor 10 Tagen bei Jooble gefunden
WebMD
• Berlin Berlin, DE
Absolventen, Einsteiger, Trainees Homeoffice möglich Abgeschlossenes Studium
Betriebliche Altersvorsorge Sabbaticals 30+ Urlaubstage Work-Life-Balance
[. .. ] project steps. Cross-Functional Coordination: You orchestrate the flow of information between international stakeholders and local project teams, ensuring that campaign goals are aligned and deadlines are met. [...]
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[...] Reporting Coordination Quality Control: You act as the final checkpoint for campaign reports, ensuring data accuracy before distributing them to the respective stakeholders and partners. Consultative Support: You support the sales team in client meetings by providing technical expertise on media inventory and targeting options. WHAT YOU BRING TO THE TABLE Media Tech Affinity: [. .. ] cross-functional teams, we develop projects and new products with a clear goal: more dialog for better medicine-within the medical profession, but also between the medical profession and the pharmaceutical industry. We create an environment in which practice-relevant medical knowledge is easily accessible and available when it is really needed. By submitting your application, you confirm that you have taken note of the data protection guidelines. Als Media Operations Specialist (m/w/d) trägst du maßgeblich zur Gestaltung und Weiterentwicklung unserer Ärzte Community bei und schaffst eine Umgebung, die echten Mehrwert in der Digital Health Branche schafft. Du bist das Rückgrat unserer Kampagnenausführung und stellst eine reibungslose Mediaplanung sowie die technische Umsetzung auf unseren Plattformen sicher. Du agierst als zentrale [. .. ]
Job am 24.04.2026 bei Jooble gefunden
QC Inspector (m/f/d) - Quality Control
• Thüringen Jena, DE
Work-Life-Balance
QC Inspector (m/f/d) -
Quality Control Location: Jena Department: Quality Control Full-time Shift Work-morning and afternoon As a QC Inspector, you play a pivotal role in ensuring the highest quality [...]
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[...] standards of our products. You will work closely within our QC team to support production processes, incoming goods inspections, documentation, and continuous improvement activities. [. .. ] teams (e. g. , R D, Complaints, Validation) Support general daily tasks when needed Qualifications Requirements Completed vocational training, ideally in a technical or craft profession Work experience in the pharmaceutical or medical device industry is an advantage Fast learner with strong attention to detail Team-oriented mindset with a strong focus on quality Basic English skills (B1) for everyday work communication and understanding of simple documents (e. g. , delivery notes or instructions) Very good German skills (B2) Proactive attitude [. .. ] to Kita and other child support Ready to shape quality with us We look forward to receiving your application Please send your documents to. About Occlutech Occlutech is a leading specialist provider of minimally invasive cardiac devices, with a mission to improve the quality of life for people with heart conditions. The vision is to become a global leading specialist provider in cardiac devices, addressing congenital heart defects, stroke prevention, and heart failure. Occlutech has a broad and proven portfolio, based [. .. ]
Job gestern bei Jobleads gefunden
• Köln, Nordrhein- Westfalen Koeln
Overview Lab Connect improves lives by partnering with
pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are [...]
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[...] an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailormade, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. [. .. ] extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. Job Summary The Clinical Sample Specialist is responsible for sample management activities for samples arriving at Lab Connect Cleveland facility. The role will perform tasks in support of receiving specimens for storage, onsite processing, or shipments to partner laboratories or other facilities. The role will also communicate with other departments such as Client Services (CS) , [. .. ] and attention to detail. Sample shipment receipt, inbound tracking documentation, and breakdown of kits received. Specimen transport to different areas within the facility. Order requisition registration and accessioning. Assist with quality control (QC) of specimens for courier pickups, scheduled shipments, ad hoc shipments, specimen destructions, and sameday shipping packages. Identification of sample discrepancies and ability to follow appropriate escalation paths. Assist with QC checks on specimens from storage for shipments and destruction. Handling, recycling and disposal of dry ice. Storage freezer and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
PEV Qualification Engineer
• Wuppertal, Nordrhein- Westfalen
[. .. ] to, equipment/ instrument/ CTU commissioning/ qualification/ re-qualification, shipping validation, cleaning validation. Support the PEV department to maintain the qualification and validation status of the equipment and system. [...]
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[...] Implement the quality event, such as QDV, deviation, change control, CAPA. Responsibilities Manage and coordinate commissioning, qualification, validation, re-qualification and periodic review activities. Prepare qualification plans, protocols and reports, risk assessment and other CQV related documents. Plan and execute equipment/ system qualification, as well as sanitisation, cleaning, shipping validation in cooperation with system/process owners, contractors and suppliers. Perform [. .. ] sharing to other team members. The employee is the deputy of the position PEV engineer and junior PEV engineer for the following responsibilities. Qualifications Bachelor of chemical engineering, biological engineering, pharmaceutical engineering or similar disciplines. Minimum of 2 years of hands-on and management in C Q, manufacturing, engineering in pharmaceutical/ biopharmaceutical industry. Knowledge in GXP regulatory requirements and industry standards related to biopharmaceutical industry, such as NMPA/ EMA/ PICs GMP, 21CFR Part 11/ 210/ 211, Annex 11 and Annex 15 [. .. ] depth knowledge and experience in GMP, quality, EHS. Strong collaboration, self-motivation, communication and influence. Good knowledge on MC office application. The employee is the deputy of the position CSV specialist for the following responsibilities. Responsibilities similar to that of PEV engineer. The deputy of the employee is PEV engineer or head of validation or CSV specialist for the following responsibilities. All the responsibilities of a PEV engineer. As we extend our global reach, we need colleagues interested in change, in [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Mantell Associates is partnered with a confidential, globally recognized organization seeking a strategic and experienced Vice President of
Quality to lead quality assurance and continuous improvement initiatives across the [...]
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[...] DACH region. This is a fully remote leadership role with significant influence on operational excellence, regulatory compliance, and customer satisfaction at a regional and global scale. VP of Quality-Responsibilities: Define and execute the regional quality strategy aligned with global business objectives Lead and develop high-performing quality teams across Germany, Austria, and Switzerland Oversee quality assurance, quality control, and continuous improvement programs Ensure compliance with all relevant regulatory standards and industry requirements Drive a culture of quality, operational excellence, and accountability across the organization Collaborate cross-functionally with operations, supply chain, R D, and commercial teams Act as a key member of the senior leadership team, contributing to [. .. ] remote working model with flexibility Opportunity to shape quality strategy at a regional and global level Collaborative, forward-thinking organizational culture Significant leadership visibility and impact Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0) 20 3854 7700. #J-18808-Ljbffr 90556290 [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Senior Design Manager
• Nordrhein- Westfalen
Senior Design Manager Technical Facilities Location: Germany Sector: Data Centres
Pharmaceutical High-Tech/ Industrial The Role A leading international general contractor is seeking an experienced Design Manager to support the [...]
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[...] delivery of complex technical facilities projects in Germany. The Design Manager will play a critical role in managing and coordinating all construction and design deliverables, ensuring alignment with construction requirements, programme, [. .. ] construction and design deliverables in line with construction requirements and the Clients expectations Coordinate all construction and design matters between key project stakeholders, including the Client, Design Team, third-party specialist designers, Contractor, and Design/ Project Director Review and monitor the Design Teams and contractors construction and design processes, procedures, and quality management plans Ensure timely distribution of all construction and design information and documentation to relevant parties Manage the review of key design milestone deliverables, ensuring quality, constructability, and coordination of design changes Implement and oversee Quality Assurance processes in line with the design consultants contracted scope of services Review and recommend control sample requirements and coordinate approvals with the Design Team, Client, and Contractor Review and manage construction and design-related queries through to amicable resolution Manage, coordinate, and control all meetings relating to construction, design, and specialist contractor shop drawings, ensuring full integration with overall project design requirements Requirements Proven experience [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Großbeeren, Brandenburg
[. .. ] impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. We are [...]
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[...] currently hiring a Quality Assurance Specialist to join our team in Grossbeeren, Germany. Hauptaufgaben Main Responsibilities Die Stelle des Quality Assurance Specialist ist der Stelle des Senior Quality Assurance Specialists unterstellt und trägt keinerlei Personalverantwortung. Die Hauptverantwortung des Quality Assurance Specialist beinhaltet die Sicherstellung der Erfüllung der Qualitätssiccherungsanforderungen gemäß dem GMP-Leitfaden, den Kundenanforderungen und sonstigen [. .. ] mit mehrjähriger einschlägiger Erfahrung oder Masterabschluss oder vergleichbar im pharmazeutischen, naturwissenschaftlichen oder technischen Bereich Completed vocational training with several years of relevant experience or Masters degree or equivalent in the pharmaceutical, scientific or technical field Gute Deutsch-und/oder Englischkenntnisse in Wort und Schrift Good written and spoken German and/or English skills Gute Kenntnisse in MS Office (Excel, Word und Outlook) Good knowledge of MS Office (Excel, Word and Outlook) GMP-Kenntnisse oder Kenntnisse in vergleichbaren Regularien sind vorteilhaft GMP [. .. ] (CAPAs) and the preparation of final reports. Koordination von Änderungskontrollen; Weiterverfolgung von Änderungskontrollmaßnahmen mit den jeweiligen Maßnahmenverantwortlichen und Sicherstellung des rechtzeitigen Abschlusses Coordination of change controls; following up on change control actions with respective action owners and ensuring timely completion Abteilungsübergreifende Kommunikation und Problemlösung unter Berücksichtigung der europäischen GMP-Richtlinien. Interdepartmental communication and problem solving in due consideration of the European GMP guidelines. Erstellung, Überarbeitung und Überprüfung von SOPs, Arbeitsanweisungen und Formularen. Draft, rework and review of SOPs, Work Instructions and [. .. ]
Job am 25.04.2026 bei Jobleads gefunden
Accounting Specialist
• Köln, Nordrhein- Westfalen
Overview Lab Connect improves lives by partnering with
pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are [...]
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[...] an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailormade, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. [. .. ] an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. Job Summary The Account Specialist is responsible for supporting monthly, quarterly, and annual financial and accounting activities, including General Ledger support (balance sheet and P L) , Accounts Payable (AP) , Accounts Receivable (AR) , and VAT declarations for Lab Connect. This role supports AP and AR processes by identifying and resolving alignment issues and [. .. ] completeness, and compliance with internal controls and reporting standards Assist with the preparation of financial statements and internal management reports Perform intercompany reconciliations and support resolution of variances Support inventory control activities, including cycle counts, pricing validation, and process documentation Coordinate VAT filing processes in partnership with external advisors and the Finance Director Assist the Finance Director with data preparation and support related to corporate income tax filings Support analysis of business operations, costs, and revenues to assist with forecasting and [. .. ] as one global team, we strive to ensure that every individual has the opportunity to thrive and contribute to our shared success. Benefits We truly live our values: People First, Quality Focused, Customer Centered, Technology Driven, Accountability Always The opportunity to make a meaningful impact on a passionate and growing team Strong communication and collaboration within a smaller sized team Access to tools and resources that empower you to excel in your role #J-18808-Ljbffr 89581369 [. .. ]
Job am 13.04.2026 bei Jobleads gefunden
• Holzminden, Niedersachsen
Symrise is a global supplier of fragrances and flavours, cosmetic active ingredients as well as functional ingredients. Its customers include perfume, cosmetics, food and beverage manufacturers, the
pharmaceutical industry [...]
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[...] and producers of dietary supplements and pet food. With sales of around 5.0billion in the 2024 financial year, the company is one of the worlds leading providers. The Group, headquartered in Holzminden, Germany, has more than 100 locations in Europe, Africa and the Middle East, Asia, the USA [. .. ] new ideas and marketready concepts for products that form an indispensable part of everyday life. Economic success and corporate responsibility are inextricably linked. Your Role We are looking for a Specialist Regulatory Affairs Flavor-Animal Feed/Pet Food to strengthen our Regulatory Affairs Flavor team. In this role, you ensure the regulatory compliance of raw materials, additives, and finished products for animal feed and pet food, with a strong focus on EU legislation. The position also covers regulatory screening, impact assessment, [. .. ] documentation and customer dossiers. Support product development and commercialization by providing regulatory guidance from concept to market launch. Act as the regulatory contact for internal stakeholders such as R D, Quality, Sales, and Marketing. Interface with external partners, customers, industry associations, and authorities. Manage regulatory change control processes, including legal updates and raw material changes. Support audits, inspections, and customer inquiries related to regulatory topics. About You University degree in Food Science, Food Technology, Veterinary Medicine, Animal Nutrition, Chemistry, Biology, or a comparable scientific discipline. Experience in Regulatory Affairs for Animal Feed and/or Pet Food, either [. .. ]
Job am 29.03.2026 bei Jobleads gefunden
Maintenance Execution Professional L1-2
• Verna, Hessen
About the job The Maintenance Reliability
Specialist plays a critical role in ensuring optimal plant performance and equipment reliability within Sanofis
pharmaceutical manufacturing environment. This position is responsible [...]
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[...] for driving maintenance excellence, implementing predictive maintenance strategies, and ensuring compliance with stringent regulatory standards including c GMP, GXP, and GDP. The specialist will leverage technical expertise, data analytics, and reliability engineering principles to maximize equipment uptime, minimize unplanned downtime, and support continuous improvement initiatives that directly impact product quality and patient safety. Main responsibilities Overall plant reliability: Ensure optimal performance and availability of equipment, utilities, and facilities across the manufacturing site. Monitoring of MR value, performance, and cost effectiveness: Track key reliability metrics, analyze performance trends, and optimize maintenance expenditure. Maintenance strategy and continuous optimization: Develop, implement, and refine [. .. ] investigation, CAPA implementation. Regulatory audit handling and CAPA implementation of the same. Ensure to coordinate with Quality Assurance for implementation of Corrective actions and preventive actions for Quality events. Change Control management: Logging of change control and ensure to close the same after completion of activity in defined time. SOP revision for routine revision and Inclusion of corrective actions and preventive actions. Training and Development Confirm that you are trained on relevant SOPs before proceeding for execution of the activity. Train [. .. ]
Job am 29.03.2026 bei Jobleads gefunden
• Hamburg
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water
quality [...]
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[...] environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. Job Description Job Summary Chart World has rapidly grown to become one of the worlds largest specialist digital-navigation providers. We pride ourselves on being true experts in our field. This is reflected in the products, services, and technology that we deliver to our merchant marine and cruise clients. Since our early beginnings in Hamburg, Germany, we have expanded to offices around the globe, including Singapore, Tokyo, [. .. ] exportcontrolled information or items (i. e. regulated technology or technical data per ITAR/ EAR U. S. regulations) . Applicants must be eligible to apply for and obtain the appropriate export control license from the U. S. Departments of State or Commerce. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is [. .. ]
Job am 28.03.2026 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 [. .. ]
Job am 23.03.2026 bei Jobleads gefunden
[. .. ] for the mediocre. Each of us is driven to help improve patients lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your [...]
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[...] role As Senior Specialist (m/f/d) - Quality Assurance/ Regulatory Affairs you are responsible for the local implementation of regulatory strategies, obtain and maintain marketing authorizations for product (s) and communication of local regulatory requirements in support of licensing of the products. Support regulatory activities relating to specific portfolio of Kidney Care (chronic and acute) products/ projects. You [. .. ] compliance with local regulations Prepare SOPs to reflect specific local requirements Implement and maintain the local Quality System, Support QA related processes: NCR and CAPA activities and timely implementation Change Control activities Timely implementation of Field Actions (FA) Local activities for Supplier qualification and management Local documentation (SOPs, periodic reviews, implement global documentation at local level) Support preparation and execution of Quality/ Management Reviews Perform Customer Eligibility checks (Customer and Supplier Approvals) Support Internal audit program planning and execution Ensure readiness [. .. ] Third Party Logistic provider in day-by-bay activities or specific projects. What youll bring Bachelors degree in scientific discipline 2-4 years regulatory, quality, or equivalent experience within a pharmaceutical and/or medical device company, CRO, CMO or similar organization Knowledge of regulations, Good Manufacturing Practices, Distribution Practices and ISO standards Scientific knowledge Project management skills Manage multiple deadlines Ability to multitask and prioritize #J-18808-Ljbffr 85378390 [. .. ]
Job am 20.03.2026 bei Jobleads gefunden
Senior Specialist (m/f/d) Quality Assurance/ Regulatory Affairs temporary December 2027
• München, Bayern
[. .. ] settle for the mediocre. Each of us is driven to help improve patients lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. [...]
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[...] Your role Senior Specialist (m/f/d) Quality Assurance/ Regulatory Affairs you are responsible for the local implementation of regulatory strategies, obtain and maintain marketing authorizations for product (s) and communication of local regulatory requirements in support of licensing of the products. Support regulatory activities relating to specific portfolio of Kidney Care (chronic and acute) products/ projects. You [. .. ] compliance with local regulations Prepare SOPs to reflect specific local requirements Implement and maintain the local Quality System, Support QA related processes: NCR and CAPA activities and timely implementation Change Control activities Timely implementation of Field Actions (FA) Local activities for Supplier qualification and management Local documentation (SOPs, periodic reviews, implement global documentation at local level) Support preparation and execution of Quality/ Management Reviews Perform Customer Eligibility checks (Customer and Supplier Approvals) Support Internal audit program planning and execution Ensure readiness [. .. ] Third Party Logistic provider in day-by-bay activities or specific projects. What youll bring Bachelors degree in scientific discipline 2-4 years regulatory, quality, or equivalent experience within a pharmaceutical and/or medical device company, CRO, CMO or similar organization Knowledge of regulations, Good Manufacturing Practices, Distribution Practices and ISO standards Scientific knowledge Project management skills Manage multiple deadlines Ability to multitask and prioritize Interpersonal and communication skills Negotiation skills Technical system skills (e. g. , word processing, spreadsheets, databases, [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
• Berlin
Construction Manager
Pharmaceutical Manufacturing Project Berlin Freelance We are seeking an experienced construction Manager to oversee the onsite delivery of a large pharmaceutical manufacturing project in Berlin, coordinating structural, [...]
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[...] MEP, cleanroom, and utility work packages. This freelance role requires strong leadership across multiple trades, ensuring GM Pcompliant execution, safety, quality, and progress reporting. Ideal candidates will have experience in pharma, biotech, data centre, or hightech projects and be fluent in English, with German preferred. Contract : Freelance-Long term project Start Date : May 2026 Immediate Languages : English required German Preferred Role Overview: Onsite coordination of contractors and specialist trades Delivery of structural, MEP, cleanroom, and utility work packages Ensuring GM Pcompliant execution and technical quality Managing timelines, progress, safety, and reporting Working closely with project directors, engineering teams, and QA What Were Looking For: Experience delivering pharma, biotech, data centre, chemical, or hightech manufacturing projects Strong leadership on [. .. ] systems, structural works, and construction sequencing Proven ability to lead subcontractors and coordinate multidiscipline teams Skilled in site logistics, planning, scheduling, and daily operations Strong focus on health safety, quality control, and compliance Excellent communication, problemsolving, and stakeholder management If this fits your skills experience, please apply or send your CV to #J-18808-Ljbffr 82168048 [. .. ]
Job am 16.02.2026 bei Jobleads gefunden
Senior Project Director (m/f/d) - Group Project Management
Führungs-/ Leitungspositionen
[. .. ] new comprehensive production facility, thereby enabling significant expansion across the entire global company. This strategic leadership role ensures compliant, on-time, and on-budget delivery of a complete large-scale [...]
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[...] pharmaceutical manufacturing program. Join us in shaping our vision to provide new health solutions advancing human life. Your main tasks and responsibilities Lead and govern large-scale pharmaceutical capital EPC projects (greenfield, brownfield, expansions) , serving as the primary interface to executive leadership and key stakeholders Define and execute project strategy, [. .. ] execution model, master schedule, budget across all project phases Oversee end-to-end project delivery, from engineering and construction through commissioning, qualification, validation (CQV) and operational handover Ensure regulatory and quality compliance in line with FDA, EMA, and GMP requirements, partnering closely with Quality and Regulatory Affairs Manage financial performance and risk, including CAPEX planning, cost control, change management and major procurement decisions Lead cross-functional and external teams, coordinating subprojects, internal functions and managing EPC/ EPCM partners, contractors and suppliers Your expertise and ideal skill set Degree in Engineering, Natural Sciences or a comparable technical discipline 15+ years of experience and proven track record leading pharmaceutical [. .. ] local PMOs at the production sites, are jointly responsible for the planning, management, and implementation of projects within the Octapharma Group. As such, we serve as a link between the specialist departments and external partners. Our mission is to ensure schedule, cost, and quality targets are met in all project phases using established project management methods. Structured knowledge transfer, lessons learned, and ongoing optimization of project processes and tools are promoted in our department. Thrive with us Company restaurant meal subsidy [. .. ]
Job am 26.12.2025 bei Jobleads gefunden
Application Specialist (m/f/d) / SAP-/ MES-Key User (w/f/d) Pharma Production
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Europe 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 [. .. ]
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 21 offene Stellenanzeigen für Pharmaceutical Quality Control Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Quality Control Specialist Jobs?
Aktuell suchen 5 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:
- CTC Resourcing Solutions (2 Jobs)
- Octapharma Austria (1 Job)
- DNHK (1 Job)
- WebMD (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 Nordrhein-Westfalen (5 Jobs), Bayern (2 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Quality Control Specialist Jobs?
Pharmaceutical Quality Control Specialist Jobs gehören zum Berufsfeld Qualitätswesen.
