$119.78 - $149.72/hr
BeiGene, Ltd. is looking for a Senior Pharmaceutical Affairs Manager based in Germany. The ... quality assurance processes. The job offers a salary range of 103,200.00 EUR to 129,000.00 EUR ...

$119.78 - $149.72/hr
BeiGene, Ltd. is looking for a Senior Pharmaceutical Affairs Manager based in Germany. The ... quality assurance processes. The job offers a salary range of 103,200.00 EUR to 129,000.00 EUR ...
$119.78 - $149.72/hr
BeiGene, Ltd. is looking for a Senior Pharmaceutical Affairs Manager based in Germany. The ... quality assurance processes. The job offers a salary range of 103,200.00 EUR to 129,000.00 EUR ...
Conduct and support Quality Assurance (QA) activities related to applicable PV regulatory requirements, guidelines, laws and internally established standards, procedures and practices for all phases ...
Conduct and support Quality Assurance (QA) activities related to applicable PV regulatory requirements, guidelines, laws and internally established standards, procedures and practices for all phases ...
Partner with manufacturing, quality assurance, quality control, regulatory affairs, clinical operations, development, patient safety and other stakeholders to ensure timely and thorough management of ...
Partner with manufacturing, quality assurance, quality control, regulatory affairs, clinical operations, development, patient safety and other stakeholders to ensure timely and thorough management of ...
... Quality, Assurance, and Lifecycle Governance * Perform data profiling, mapping, cleaning ... transformation, source-to-report reconciliation, and root-cause analysis to confirm the accuracy ...
... Quality, Assurance, and Lifecycle Governance * Perform data profiling, mapping, cleaning ... transformation, source-to-report reconciliation, and root-cause analysis to confirm the accuracy ...
Drive high-quality strategic feasibility/site identification assessments based on Standard of Care ... support BeiGene R&D goals. Supervisory Responsibilities: * Support training and development of ...
Drive high-quality strategic feasibility/site identification assessments based on Standard of Care ... support BeiGene R&D goals. Supervisory Responsibilities: * Support training and development of ...
Partner with software engineering and QA from product conception to embed compliance into Agile/Scrum lifecycles. * Oversee the authoring of critical validation deliverables (URS, FS, Risk ...
Partner with software engineering and QA from product conception to embed compliance into Agile/Scrum lifecycles. * Oversee the authoring of critical validation deliverables (URS, FS, Risk ...
Hopewell, NJ · On-site
$90K - $125K/yr
Perform QC Chemistry laboratory activities with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished ...
Hopewell, NJ · On-site
$90K - $125K/yr
Perform QC Chemistry laboratory activities with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished ...
In collaboration with QA, Corporate Compliance, GCO & Development peers/associates, identify root causes for major and critical observations, devise relevant remedial and improvement actions for ...
In collaboration with QA, Corporate Compliance, GCO & Development peers/associates, identify root causes for major and critical observations, devise relevant remedial and improvement actions for ...
$119.78 - $149.72/hr
Creates and reviews GxP relevant local governance documents within the RA and QA area, supports other functions (e.g. PV, Medical) in relation to creation and review of GxP relevant governance ...
$119.78 - $149.72/hr
Creates and reviews GxP relevant local governance documents within the RA and QA area, supports other functions (e.g. PV, Medical) in relation to creation and review of GxP relevant governance ...
$153K - $202K/yr
In-depth knowledge of ICH guidelines and global Regulatory CMC requirements; familiarity with GMP and Quality Assurance regulations is a plus. * Extensive experience authoring, reviewing, and ...
$153K - $202K/yr
In-depth knowledge of ICH guidelines and global Regulatory CMC requirements; familiarity with GMP and Quality Assurance regulations is a plus. * Extensive experience authoring, reviewing, and ...
Hopewell, VA · On-site
$175 - $235/hr
Cross-functional collaboration experience with key stakeholders including Manufacturing Operations, Quality Assurance/ Control (QA/QC), Facilities and Engineering (F&E) and Regulatory Compliance ...
Hopewell, VA · On-site
$175 - $235/hr
Cross-functional collaboration experience with key stakeholders including Manufacturing Operations, Quality Assurance/ Control (QA/QC), Facilities and Engineering (F&E) and Regulatory Compliance ...
Pennington, NJ · On-site
$174K - $234K/yr
Cross-functional collaboration experience with key stakeholders including Manufacturing Operations, Quality Assurance/ Control (QA/QC), Facilities and Engineering (F&E) and Regulatory Compliance ...
Pennington, NJ · On-site
$174K - $234K/yr
Cross-functional collaboration experience with key stakeholders including Manufacturing Operations, Quality Assurance/ Control (QA/QC), Facilities and Engineering (F&E) and Regulatory Compliance ...
Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate * Collaborates with CST members and colleagues to ensure cross-team, site ...
Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate * Collaborates with CST members and colleagues to ensure cross-team, site ...
Hopewell, NJ · On-site
$25.48 - $33.48/hr
Performing in-process visual inspection for quality assurance * Labeling and packaging of finished drug product in compliance with cGMP * Completing batch documentation and reviewing records for ...
Hopewell, NJ · On-site
$25.48 - $33.48/hr
Performing in-process visual inspection for quality assurance * Labeling and packaging of finished drug product in compliance with cGMP * Completing batch documentation and reviewing records for ...
Prepares sites for quality assurance audits and inspections, drives responses to audit and ... Works with integrity and ethically in accordance with BeiGene's Code of Business Conduct and Ethics ...
Prepares sites for quality assurance audits and inspections, drives responses to audit and ... Works with integrity and ethically in accordance with BeiGene's Code of Business Conduct and Ethics ...
Pennington, NJ · On-site
$110K - $150K/yr
Partner with QA on: * Batch record review * Deviations, CAPAs, and investigations * Maintain inspection readiness (FDA / regulatory audits) * Ensure proper serialization and traceability systems ...
Pennington, NJ · On-site
$110K - $150K/yr
Partner with QA on: * Batch record review * Deviations, CAPAs, and investigations * Maintain inspection readiness (FDA / regulatory audits) * Ensure proper serialization and traceability systems ...
$72K - $97K/yr
... Management Associates and other key stakeholders globally and regionally * Knowledgeable of ... Suggest improvements to enhance efficiency and the quality of the work performed on assigned ...
$72K - $97K/yr
... Management Associates and other key stakeholders globally and regionally * Knowledgeable of ... Suggest improvements to enhance efficiency and the quality of the work performed on assigned ...
Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate * Collaborates with CST members and othercolleagues to ensure cross-team ...
Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate * Collaborates with CST members and othercolleagues to ensure cross-team ...
Cambridge, MA · On-site
Support any additional assignments or special projects as required, including but not limited to External/Internal Quality Assessment, Quality Assurance and Improvement Program (QAIP) and audit ...
Cambridge, MA · On-site
Support any additional assignments or special projects as required, including but not limited to External/Internal Quality Assessment, Quality Assurance and Improvement Program (QAIP) and audit ...
... Quality Assurance, Supply Chain, CMC, and IT. The focus of the internship is for the intern to develop a deeper understanding of the drug development process and regulatory requirements in a ...
... Quality Assurance, Supply Chain, CMC, and IT. The focus of the internship is for the intern to develop a deeper understanding of the drug development process and regulatory requirements in a ...

$119.78 - $149.72/hr
Other
Posted 8 days ago
BeiGene, Ltd. is looking for a Senior Pharmaceutical Affairs Manager based in Germany. The successful candidate will oversee local Pharmaceutical Affairs operations, manage GxP compliance, and support regulatory inspections. This role requires strong leadership skills and a deep understanding of the regulatory environment.
Ideal applicants will have over 7 years of relevant experience, be fluent in both German and English, and possess expertise in regulatory affairs and quality assurance processes.
The job offers a salary range of 103,200.00 EUR to 129,000.00 EUR, with an expected travel of approx. 10%.
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BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .
Health care and social assistance
5,001 - 10,000 Employees
Cambridge, MA, US
2010