29 Jobs für Pharmaceutical Quality Control Specialist
Stellenangebote Pharmaceutical Quality Control Specialist Jobs
Job vor 13 Tagen bei F.A.Z. Stellenmarkt gefunden
Alliance Medical RP GmbH
• 53117, Bonn
[. .. ] team. YOUR future at Alliance Medical Radiopharmacy lies in YOUR hands Our team can t wait to get to know YOU. So there s only one thing [...]
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[...] left to do: Apply CMC Quality Specialist (m/w/d) Bonn-Auerberg About us At our site in Bonn, a team of around 40 dedicated experts develops and produces state-of-the-art PET tracers that significantly improve patients lives. We combine scientific precision with a pioneering spirit-in an open, international environment where you can take ownership, [. .. ] the future of radiopharmaceuticals with vision, structure, and determination. Major Tasks Support current and new radiopharmaceutical development projects at the CMO. Assist in implementing and maintaining production processes and quality control testing. Perform risk assessments, using common concepts like, e. g. , FMEA. Assess processes to be implemented from a quality perspective and ensure that implementation complies with internal and external quality standards and policies. Perform quality control testing (HPLC, GC, TLC) . Perform validation activities (both operational procedures and computerised [. .. ] Comprehensive onboarding and training in all technical systems, including cyclotron and radiation protection technology Collaboration within a committed, professional, and friendly team Porfil On-site work required. University degree in pharmaceutical sciences, chemistry, or a related scientific discipline. Advanced knowledge of GMP requirements. At least 2 years of experience in quality control (HPLC, GC, TLC) within the pharmaceutical industry. Experience in technology transfers and analytical method validation; experience in computer system validation will be an advantage. Experience in core tools of [. .. ]
Neu Job vor 7 Std. bei Mindmatch.ai gefunden
Octapharma Pharmazeutika Produktionsges. m. b. H.
Group Expert Analytical Specialist (m/f/d) - Quality Control (m/w/d)
• Vienna
Group Expert Analytical
Specialist (m/f/d) -
Quality Control-temporary Job-ID: 62407 Location: Wien, AUT Job Level: Professionals Category: Quality Employment Type: Temporary employment Become part of a vital chain and contribute [...]
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[...] to our common goal of making peoples lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced [. .. ] us in shaping our vision of providing new health solutions advancing human life. Your main tasks and responsibilities Develop and validate analytical test methods in compliance with GMP and official pharmaceutical standards Act as Global Subject Matter Expert for Method Validation Transfer, including protocol review, risk assessment, troubleshooting, data evaluation, cross-site coordination, and reporting Establish and maintain Group-wide analytical standards, controls, and reference systems Regular exchange and communication with the test laboratory Serve as a key contact for Global [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD Österreich
• AT- 9 Wien
[. .. ] Produkte geht in den Export. Um ein nachhaltiges Unternehmenswachstum gewährleisten zu können, sind wir stets bemüht attraktive Karrieremöglichkeiten für die mehr als 450 Mitarbeiter in unserem Unternehmen [...]
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[...] anzubieten. Position Senior Specialist, Quality Assurance (m/w/d) Vollzeit, ab sofort, befristet auf 2 Jahre Responsibilities Funktion als Quality Representative im GMP-Umfeld mit Schwerpunkt Abweichungen, Änderungsanträge, CAPAs, bzw. Lead Investigator von Reklamationen inkl. Erstellung, Bearbeitung und Steuerung Übernahme der Quality Representative Rolle insbesondere für QC-bezogene Vorgänge, z. B. OOS/ OOT Fälle, Methoden [. .. ] Rolle Key Skills Adaptability Audit Internal Controls Biopharmaceutical Industry c GMP Regulations Change Management Chemical Biology Communication Cross Team Collaboration Deviation Management Good Automated Manufacturing Practice (GAMP) KPI Analysis Manufacturing Quality Control Medicinal Chemistry Pharmaceutical Microbiology Pharmaceutical Quality Assurance Pharmaceutical Sciences Pharmacodynamics Process Improvements Product Disposition Quality Assurance (QA) Quality Assurance (QA) Standards Quality Auditing Quality Management Standards Quality Standards Benefits Spannendes und abwechslungsreiches Arbeitsfeld in einem modernen, international agierenden Unternehmen Jahresbonus sowie Mitarbeiteranerkennungsprämien Mitarbeiterempfehlungsprogramm Attraktive Firmenpension Bezahlte Elternzeit vom Unternehmen im Ausmaß von 12 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD Österreich
Senior Specialist, Market Access (m/f/d)
• AT- 9 Wien
[. .. ] continually striving to improve the understanding of health care within the local community. Our site in 1100 Vienna (ICON TOWER) is a strategic location for the distribution [...]
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[...] of our high quality and innovative health care products, as well as digitally integrated solutions for our patients and clients. To ensure sustainable company growth, we continually aim to offer attractive career opportunities for more than 170 employees at our Vienna site. Responsibilities Support and drive the preparation of pricing strategies (in cooperation with [. .. ] Austrian reimbursement code (Erstattungskodex, EKO) , including preparation and coordination of EKO listing submissions and crossfunctional input for the evaluations by HEK/ Dachverband Develop economic and qualityoflife models for innovative pharmaceutical products to national payers and other stakeholders Is responsible for any legal notifications (index of goods and contract management) Develop risksharing programs for new drugs and proactively offer these programs to potential payors (pharmaecomonic studies, HTA) and access decision makers (hospitals social insurances) Closely liaise with the marketing organization for [. .. ] Responsible AI, and basic AI agents) via internal learning opportunities Able to use Gen AI to accelerate analysis work (e. g. , firstdraft synthesis, scenario framing, structured summaries) without compromising quality control and critical thinking Required Skills Access Management Accountability Adaptability Building Materials Cost Effectiveness Analysis Data Analysis Direct Marketing Economics Finance Financial Advising Global Market Healthcare Reimbursement Health Economic Modeling Health Economics Health Economics Research Health Policy Analysis Health Technology Assessment (HTA) Hospital Management Interpersonal Relationships Management Process Market Access Marketing [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD Malaysia
• AT- 9 Wien
[. .. ] continually striving to improve the understanding of health care within the local community. Our site in 1100 Vienna (ICON TOWER) is a strategic location for the distribution [...]
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[...] of our high quality and innovative health care products, as well as digitally integrated solutions for our patients and clients. To ensure sustainable company growth, we continually aim to offer attractive career opportunities for more than 170 employees at our Vienna site. Responsibilities: Support and drive the preparation of pricing strategies (in cooperation with [. .. ] (Erstattungskodex, EKO) , including preparation and coordination of EKO listing submissions and cross-functional input for the evaluations by HEK/ Dachverband Develop economic and quality-of-life models for innovative pharmaceutical products to national payers and other stakeholders Is responsible for any legal notifications (index of goods and contract management) Develop risk-sharing programs for new drugs and pro-actively offer these programs to potential payors (pharmaecomonic studies, HTA) and access decision makers (hospitals social insurances) Closely liaise with the marketing [. .. ] AI, and basic AI agents) via internal learning opportunities Able to use Gen AI to accelerate analysis work (e. g. , first-draft synthesis, scenario framing, structured summaries) without compromising quality control and critical thinking We offer an attractive salary, outstanding social benefits and an exciting work environment with varied tasks in an international environment. The minimum annual salary for this position is EUR 74.600, --and varies according to the qualifications and experience of the successful candidate. Please note that this [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
MSD Malaysia
Senior Specialist, Quality Assurance (m/w/d)
• AT- 9 Wien
[. .. ] zu können, sind wir stehts bemüht attraktive Karrieremöglichkeiten für die mehr als 450 Mitarbeiter in unserem Unternehmen anzubieten. Zur Unterstützung unseres Teams in Wien suchen wir ab [...]
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[...] sofort einen Senior Specialist, Quality Assurance (m/w/d) befristet auf 2 Jahre in Vollzeit. Senior Specialist, Quality Assurance (m/w/d) Vollzeit, ab sofort, befristet auf 2 Jahre Zu Ihrem Aufgaben- und Verantwortungsbereich in dieser Position zählen: Funktion als Quality Representative im GMP-Umfeld mit Schwerpunkt: Abweichungen, Änderungsanträge, CAPAs, bzw. Lead Investigator von Reklamationen [. .. ] Skills: Adaptability, Adaptability, Audit Internal Controls, Biopharmaceutical Industry, c GMP Regulations, Change Management, Chemical Biology, Communication, Cross-Team Collaboration, Deviation Management, Good Automated Manufacturing Practice (GAMP) , KPI Analysis, Manufacturing Quality Control, Medicinal Chemistry, Pharmaceutical Microbiology, Pharmaceutical Quality Assurance, Pharmaceutical Sciences, Pharmacodynamics, Process Improvements, Product Disposition, Quality Assurance (QA) , Quality Assurance (QA) Standards, Quality Auditing, Quality Management Standards, Quality Standards + 5 more Preferred Skills: Current Employees apply Current Contingent Workers apply Search Firm Representatives Please Read Carefully Merck Co. , Inc. , Rahway, [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Merck
Senior Specialist, Quality Assurance (m/w/d)
• AT- 9 Wien
[. .. ] zu können, sind wir stehts bemüht attraktive Karrieremöglichkeiten für die mehr als 450 Mitarbeiter in unserem Unternehmen anzubieten. Zur Unterstützung unseres Teams in Wien suchen wir ab [...]
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[...] sofort einen Senior Specialist, Quality Assurance (m/w/d) befristet auf 2 Jahre in Vollzeit. Senior Specialist, Quality Assurance (m/w/d) Vollzeit, ab sofort, befristet auf 2 Jahre Zu Ihrem Aufgaben- und Verantwortungsbereich in dieser Position zählen: Funktion als Quality Representative im GMP-Umfeld mit Schwerpunkt: Abweichungen, Änderungsanträge, CAPAs, bzw. Lead Investigator von Reklamationen [. .. ] Skills: Adaptability, Adaptability, Audit Internal Controls, Biopharmaceutical Industry, c GMP Regulations, Change Management, Chemical Biology, Communication, Cross-Team Collaboration, Deviation Management, Good Automated Manufacturing Practice (GAMP) , KPI Analysis, Manufacturing Quality Control, Medicinal Chemistry, Pharmaceutical Microbiology, Pharmaceutical Quality Assurance, Pharmaceutical Sciences, Pharmacodynamics, Process Improvements, Product Disposition, Quality Assurance (QA) , Quality Assurance (QA) Standards, Quality Auditing, Quality Management Standards, Quality Standards + 5 more Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck Co. , Inc. [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Octapharma Austria
Global QC Method Validation Expert GMP, Analytics
• AT- 9 Wien
A leading
pharmaceutical company in Vienna is seeking a Group Expert Analytical
Specialist to drive innovation in Group
Quality Control. The role involves developing and validating analytical methods, acting [...]
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[...] as a global expert for method validation, and establishing analytical standards. Candidates should have a natural sciences degree and experience in GMP environments. The position is temporary, covering maternity leave until April 30, 2028, and offers competitive benefits while promoting diversity [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
Octapharma Austria
• AT- 9 Wien
Job-ID: 62407 Location: Wien, AUT Job Level: Professionals Category:
Quality Employment Type: Temporary employment Become part of a vital chain and contribute to our common goal of making peoples [...]
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[...] lives 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 privately-owned [. .. ] scale of a global organisation. With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location. As a Group Expert Analytical Specialist, you will drive innovation and continuous improvement initiatives within Group Quality Control. The position is temporary until April 30, 2028 due to maternity leave coverage. Join us in shaping our vision of providing new health solutions advancing human life. Your Main Tasks And Responsibilities Develop and validate analytical test methods in compliance with GMP and official pharmaceutical standards Act as Global Subject Matter Expert for Method Validation Transfer, including protocol review, risk assessment, troubleshooting, data evaluation, cross-site coordination, and reporting Establish and maintain Group-wide analytical standards, controls, and reference systems Regular exchange and communication with the test laboratory Serve as a key contact for Global [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Octapharma
Group Expert Analytical Specialist (m/f/d) - Quality Control-temporary
• AT- 9 Wien
Group Expert Analytical
Specialist (m/f/d) -
Quality Control-temporary Job ID: 62407 Location: Wien, AT Job Level: Professionals Job Category: Quality Employment Type: Temporary employment Become part of a vital [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] chain and contribute to our common goal of making peoples lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines [. .. ] The position is temporary until April 30, 2028 due to maternity leave coverage. Your main tasks and responsibilities Develop and validate analytical test methods in compliance with GMP and official pharmaceutical standards Act as Global Subject Matter Expert for Method Validation Transfer, including protocol review, risk assessment, troubleshooting, data evaluation, cross-site coordination, and reporting Establish and maintain Group-wide analytical standards, controls, and reference systems Regular exchange and communication with the test laboratory Serve as a key contact for Global [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Inova Consulting SA
• AT- 2 Schweiz
About Us Inova is a premier
pharmaceutical consulting firm based in Switzerland, known for delivering cutting-edge solutions in the pharma industry. Our team of experts specializes in guiding pharma [...]
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[...] companies through complex regulatory landscapes and ensuring the highest standards of product quality and safety. Job Description The Quality Control Specialist at Inova plays a key role in overseeing laboratory operations, ensuring compliance with regulatory standards, and driving continuous improvement initiatives. This position focuses on maintaining and enhancing quality processes while collaborating with cross-functional teams to ensure optimal product control and operational efficiency. Key Responsibilities Laboratory Oversight : Lead laboratory [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Inova Consulting SA
Senior QC Specialist, Pharma Biotech
• AT- 2 Schweiz
A leading
pharmaceutical consulting firm in Austria is looking for a
Quality Control Specialist to oversee laboratory operations, ensuring compliance with regulatory standards and driving process improvements. The ideal [...]
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[...] candidate will have at least 5 years of experience in a quality control lab, a relevant degree, and expertise in analytical techniques like HPLC. This role offers a competitive salary, professional growth opportunities, and the [. .. ]
Job am 14.02.2026 bei Mindmatch.ai gefunden
Octapharma
• AT- 9 Wien
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 gestern 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. Department Description As PEV Qualification Engineer, you will be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives. In this role you will report to the Head of PEV. Manage and coordinate commissioning, qualification, validation, re-qualification [. .. ] perform activities as per risk assessments where required. Receive and complete training in time. Provide training or knowledge sharing to other team members. 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 11and Annex 15 of [. .. ] position PEV engineer and junior PEV for the following responsibilities, All the responsibilities of a PEV engineer and junior PEV engineer. 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 5 Tagen bei Jobleads gefunden
[. .. ] company is growing fast and were seeking a driven Equipment Manager to jump on board and grow with us. We are a small, fastgrowing company that supports [...]
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[...] clinical and preclinical pharmaceutical development projects from Australia and around the globe. Our team of 55 scientists works closely with some of the best pharmaceutical and biotech companies and clinical research organisations. Driven by science, respected for results At Crux Biolabs, we love science. It is what unites us and drives us to help [. .. ] salary and flexible arrangements. Impactful: Shape how we work and leave a lasting impression on a growing Australian industry. A day in your new work life As a Senior Equipment Specialist you will support scientists who are helping pharmaceutical clients develop safe and effective medicines. Your direct impact will be on how smoothly our operations run and how confidently our teams work day to day. You will gain added exposure to validation activities, quality systems and operational workflows, making this ideal for someone who enjoys a handson environment with opportunities to expand into broader laboratory operations. Your day-to-day may include Managing procurement, installation, qualification, calibration and maintenance of laboratory equipment Maintaining equipment master lists and asset registers Partnering with scientists, validation and operations teams to define equipment needs and resolve issues Authoring, reviewing and maintaining equipmentrelated SOPs and supporting risk assessment, change control, deviation investigation and CAPA activities What were looking for A proactive individual who is collaborative and comfortable working autonomously in a regulated scientific environment. Bachelors degree in Life Sciences, Engineering, Laboratory Technology or related field. 5 to 8 years of experience in a regulated GCLP, GLP, GMP or ISO environment. [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 15.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
About Crown Crown is Irelands leading
specialist roofing, cladding and faade contractor and a trusted partner to clients across Ireland, the UK and Europe. Established in 1993, Crown delivers [...]
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[...] high-quality projects across a wide range of sectors including digital technology, commercial, industrial, pharmaceutical, healthcare and residential. With director-led involvement on all projects, Crown has built an excellent reputation for delivering complex, high-value works safely, on programme and defect-free. Role Overview Due to continued growth, Crown is seeking to recruit two Intermediate Quantity Surveyors to join our Commercial team on a [. .. ] Manager, the successful candidates will be responsible for the day-to-day commercial management of live projects, working closely with Project Managers, Site Managers and subcontractors to ensure strong cost control and commercial performance throughout the project lifecycle. This role requires flexibility and willingness to work abroad as project locations will vary across Europe. Key Responsibilities Manage day-to-day commercial activities on site in accordance with company procedures Prepare, monitor and control project budgets, forecasts and cost-to-complete reports [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
Senior Project Director (m/f/d) - Group Project Management
• Wien
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 08.02.2026 bei Jobleads gefunden
• Burgwedel, Niedersachsen
Overview We are seeking a detail-oriented Associate
Specialist (m/f/d) External Laboratory QC to support the
quality oversight of external and contract laboratories during a maternity leave cover period [...]
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[...] starting at 1st of March for 12 months. This role is central to ensuring that analytical data generated externally meets internal quality standards, regulatory expectations, and c GMP requirements. You will act as a key interface between internal Quality [. .. ] related to contract laboratories, representing QC as required Profile Degree or equivalent qualification in Life Sciences, Chemistry, Biotechnology, Pharmacy, or a related scientific discipline Experience working in a GMP-regulated pharmaceutical or biotechnology environment Strong hands-on experience with external or contract laboratory management and oversight Solid understanding of analytical testing (biological and/or chemical) performed by third-party laboratories Practical experience with deviation management, CAPA, and change control, particularly involving external partners Experience supporting batch release activities using externally generated QC data is highly desirable Experience with SAP and electronic Quality Management Systems Proficient in English and German Our Benefits Flexible working hours (37.5 hours/ week) and an attractive company pension scheme Competitive salary package: 13 monthly [. .. ]
Job am 03.02.2026 bei Jobleads gefunden
Senior Specialist (m/f/d) Quality Assurance/ Regulatory Affairs temporary 2 years
• München, Bayern
[. .. ] 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 Interpersonal and communication skills Negotiation skills Technical system skills (e. g. , word processing, spreadsheets, databases, [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
GMP Assurance Manager/ Specialist (m/w/d)
• Jülich, Nordrhein- Westfalen
Work-Life-Balance
[. .. ] to ensure alignment regarding GMP customer expectations and suitability in the framework of GMP guidelines Provide target group specific trainings and participate in global broadcast presentations Close [...]
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[...] collaboration with the Quality team to align on concept and proper application of existing quality systems and support their development Providing active support to colleagues in implementing requirements and translating them into solutions Expertise Degree (Bachelor, Master, Ph D) in the field of natural science, biotechnology or comparable Solid quality background, specifically with core Gx P systems like Change Control, Deviation Management, CAPA Professional experience in quality or regulatory in manufacturing pharma industry, CMO/ CDO/ CDMO companies or in industry developing, manufacturing, and marketing of equipment for use in pharmaceutical manufacturing Professional experience with specific quality tools used in pharmaceutical industry like: Computer software validation (CSV) based on the principles of e. g. 21CFR11, Equipment qualification (IQ/ OQ) Eurdalex Vol 4 Annex 15, Process Validation, Extractable/ Leachable data generation and evaluation, Critical impurities and contact material compliance (e. g. TSE) [. .. ]
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 [...]
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[...] 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 [. .. ]
Neu Job vor 7 Std. bei Neuvoo gefunden
Biocair
Senior Customer Care Representative
• Hamburg
Since 1986, Biocair has established a global reputation as a leading GDP logistics
specialist within the
pharmaceutical, biotechnology and life sciences sectors. Biocair has built up a unique, [...]
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[...] client-centric approach by employing scientists in front-line logistics positions and assembling a team of best-in-class industry experts in quality, cold chain and regulatory compliance. Biocair focuses on providing the most comprehensive time-sensitive and temperature-controlled logistics services available whilst delivering flexible, tailored, cost-effective solutions to all its clients. It is committed to delivering complete end-to-end logistics solutions through its 24/ 7 operation and global network [. .. ] complex shipment requirements. Responsibilities will include: Customer Shipment Management Engage with customers to address inquiries, provide updates, and ensure a smooth end-to-end service experience. Maintain full visibility and control of shipments while in transit, updating customers regularly and escalating exceptions where required. Collaborate with internal teams (Import, Export, Control Tower, Warehouse) to deliver efficient and compliant shipment solutions. Shipment Creation Solution Design Compile and verify shipment data received from Biocair Connect and email requests. Ensure accuracy across key shipment [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
PCI Pharma Services
Quality Assurance Specialist
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] currently hiring a Quality Assurance Specialist to join our team in Grossbeeren, Germany. Hauptaufgaben : 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 Vorgaben [. .. ] 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 16.01.2026 bei Neuvoo gefunden
Eppendorf
GMP Assurance Manager/ Specialist (m/w/d)
• Jülich, North Rhine- Westphalia
Work-Life-Balance
[. .. ] to ensure alignment regarding GMP customer expectations and suitability in the framework of GMP guidelines Provide target group specific trainings and participate in global broadcast presentations Close [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] collaboration with the Quality team to align on concept and proper application of existing quality systems and support their development Providing active support to colleagues in implementing requirements and translate them into solutions Your expertise Degree (Bachelor, Master, Ph D) in the field of natural science, biotechnology or comparable Solid quality background, specifically with core Gx P systems like Change Control, Deviation Management, CAPA Professional experience in quality or regulatory in manufacturing pharma industry, CMO/ CDO/ CDMO companies or in industry developing, manufacturing, and marketing of equipment for use in pharmaceutical manufacturing Professional experience with specific quality tools used in pharmaceutical industry like: Computer software validation (CSV) based on the principles of e. g. 21CFR11, Equipment qualification (IQ/ OQ) Eurdalex Vol 4 Annex 15, Process Validation, Extractable/ Leachable data generation and evaluation, Critical impurities and contact material compliance (e. g. TSE) [. .. ]
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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 29 offene Stellenanzeigen für Pharmaceutical Quality Control Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Quality Control Specialist Jobs?
Aktuell suchen 14 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:
- Merck Sharp Dohme Corp (3 Jobs)
- MSD Malaysia (2 Jobs)
- Octapharma Austria (2 Jobs)
- Octapharma (2 Jobs)
- Inova Consulting SA (2 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 Nordrhein-Westfalen (4 Jobs), Bayern (2 Jobs) und Niedersachsen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Quality Control Specialist Jobs?
Pharmaceutical Quality Control Specialist Jobs gehören zum Berufsfeld Qualitätswesen.
