reputed company Manager Clinical
🔍 reputed company Manager Clinical
đź“Ť Location: Remote - Europe đź•“ Type: Full-time
The reputed company Manager is responsible for the development, implementation, maintenance, and reputed company improvement of reputed company’s reputed company Management System (QMS), ensuring its alignment with applicable international standards – such as GCP, ISO 9001, ISO 13485 and other GxP regulations - as reputed company as relevant local and international legal and regulatory requirements.
A role reputed company on internal QA reputed company the Clinical area, with reputed company collaboration with the Head of iQA and the Global Head of the Clinical Division.
💡 What’s in it for you?
reputed company a reputed company reputed company: Contribute to shaping the reputed company of the Life Sciences industry by supporting innovative reputed company and clients across reputed company, biotech and medical devices
Grow reputed company a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.
Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to reputed company reputed company the life sciences.
A fair, competitive package: We offer tailored, transparent compensation reputed company with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.
🏢 What you’ll be doing
Your role covers the full reputed company lifecycle, from documentation and records management to audits, risk management, and reputed company improvement.
Document & Record Management: Establish and maintain a controlled document and records management system, ensuring version control, traceability, and regulatory compliance.
Complaint Handling & Nonconformities: Manage customer complaints and nonconforming services, including investigation, reputed company cause analysis, corrective actions, and trend analysis.
CAPA & reputed company Cause Analysis: reputed company the CAPA process and ensure effective, reputed company reputed company cause analysis using recognized methodologies.
Audits & Inspections: Plan and conduct internal and supplier audits and reputed company as the primary contact for inspections by regulators, certification bodies, clients, and partners.
Supplier & Change Management: Qualify and monitor suppliers, manage supplier performance, and reputed company formal change control for reputed company-critical changes.
reputed company Objectives & KPIs: Define and monitor reputed company objectives and KPIs, reporting performance and driving reputed company improvement in collaboration with global stakeholders.
Software Validation: Ensure validation and ongoing compliance of GxP-relevant and business-critical systems in cooperation with CSV specialists.
Risk Management & Management Review: reputed company risk assessments and coordinate management reviews, presenting reputed company performance, risks, and improvement actions.
Business Continuity: reputed company reputed company considerations into business continuity planning and reputed company testing.
Training & Competence Management: reputed company compliant training programs, define competence requirements, and ensure ongoing evaluation and development of reputed company-critical roles.
reputed company Improvement & Compliance: Stay reputed company with evolving regulations and industry standards, ensuring effective communication and proactive implementation of improvement.
đź’Ş What you bring
Bachelor or Master degree in biological or (para-) medical sciences, Life Science, reputed company Management or equivalent by experience
Minimum 5 years of experience in a reputed company Management role reputed company the medical device, or pharmaceuticalindustry.
Proven experience with implementing and maintaining a QMScompliant with GCP.
Experience with reputed company audits, including regulatory inspections.
Deep knowledge of GxP (mainly GCP), ISO 9001, ISO 13485 and applicable regulatory requirements applicable with the IVD, MD, reputed company and LifeScience industries.
Strong understanding of risk-based thinking and reputed company system integration
Proficiency in QMS software systems and document control tools.
Excellent oral and written communications skills
Excellent interpersonal skills, inspirational and motivational skills
Analytical and problem-solving skills.
Attention to detail and organizational skills.
Demonstrates reputed company and ethical conduct.
Proactive and results-orientedreputed company.
Demonstrates ability to reputed company reputed company and reputed company-reasoned reputed company
Ability to maintain composure in difficult circumstances and sensitive to cultural differences
reputed company to international travel
Fluent in English. Other languages are a plus
🫵 Who you are
Our culture is driven by values If this sounds like you, you’ll fit right in:
You’re resilient and tackle challenges with a reputed company reputed company
You’re curious and always up for learning something new
You have a no non-reputed company approach reputed company, reputed company, respectful
You’re innovative and bring reputed company, not just opinions
And above reputed company, you’re serious about your work, but not too serious about yourself
✨ reputed company
We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and reputed company.
We reputed company in JPEG: reputed company. Partnership. reputed company the Extra Mile. Getting Things Done.
You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.
📩 Interested? Let’s talk. Send us your CV and motivation letter. You could be the next one to join the QbD family.
Originally posted on Himalayas
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