Manager/Quality Manager
Found in: Jooble UK C2 - 2 weeks ago
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. We are looking for a full-time QA Manager to join our Quality Assurance EMEA team.
Responsibilities:- Ensure the consistent implementation, use, and review of SOPs
- Escalate issues to management in a timely manner implementing appropriate solutions, including preventative actions
- Negotiate with functional and operational internal stakeholders to improve quality and increase efficiencies
- Analyze and interpret data in order to lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
- Lead and effectively manage constructive crucial interactions with clients or regulatory agencies
- Lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
- Interpret applicable quality regulations/standards and create appropriate policies and procedures
- Ensure Regulatory Compliance and Quality Assurance (RC&QA) management responsibilities, as indicated in applicable controlled documents, are followed
- Perform other duties, as assigned by management
- 8 years in regulatory environment (experience in GXP roles)
- Experience & regulatory expertise of industry quality systems/standards
- A minimum of a Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union, or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
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Quality Assurance Manager
Found in: Talent UK C2 - 1 week ago
Maidenhead, United Kingdom Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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Found in: Jooble UK C2 - 2 weeks ago
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Engineering Manager
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Supply Chain Quality Associate
Found in: Jooble UK C2 - 2 weeks ago
Maidenhead, Berkshire, United Kingdom Proclinical Staffing Full timeSupply Chain Quality Associate - Maidenhead, England - Permanent Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England. Primary Responsibilities: The primary focus of this role is to work with internal and external stakeholders to ensure the timely release...
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Engineering Manager
Found in: Jooble UK C2 - 2 weeks ago
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Found in: Jooble UK C2 - 6 days ago
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Manager, Global Aggregate Reports quality and compliance
Found in: Talent UK C2 - 1 week ago
Maidenhead, United Kingdom CSL Full timeThe Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regulatory Intelligence Triage Manager, responsible for driving...
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Manager, Global Aggregate Reports quality and compliance
Found in: beBee S GB - 2 weeks ago
Maidenhead, United Kingdom CSL Full timeThe Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline.Responsibilities include: -Acts as a Regulatory Intelligence Triage Manager, responsible for driving initial...
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QA Manager
2 weeks ago
Maidenhead, Berkshire, United Kingdom Fortrea Full timeJob Description As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With...
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Quality and Training Technician
Found in: Jooble UK C2 - 2 weeks ago
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