Medical Device Manager jobs in Cambridge
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- SandozCambridge
- Release of medical devices and device components of combination products for clinical batch production Represent Quality Drug Delivery Device Development in…
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- ZEISS GroupCambridge
- Proven sales experience within the medical device, healthcare or life sciences sector.
- Experience selling capital medical equipment.
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View similar jobs with this employerMundipharma Research LimitedCambridge CB2 1NT- Governance & Compliance: Establish and oversee global governance frameworks, ensuring all medical activities uphold the highest ethical and scientific standards…
View similar jobs with this employerPA ConsultingMelbourn- This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
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View similar jobs with this employerPA ConsultingMelbourn- Significant experience in medical device and/or drug-device combination product development;
- This role calls for a senior engineer with substantial experience…
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- SandozCambridge
- Experience withcombination products (or device constituent parts thereof) and standalone medical devices.
- Knowledge of GMP and international device regulations;
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View similar jobs with this employerPA ConsultingMelbourn- Significant experience (typically 8+ years) within medical device industry.
- We are seeking an experienced Medical Device Quality Specialist Consultant to…
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- University of CambridgeCambridge
- The University of Cambridge, Department of Paediatrics, NeWTS team is delivering a complex, high profile medical device development programme comprising…
- MasimoCambridge CB2 0AW
- Leading on organising and running customer evaluations/deployments alongside the Account manager to educate and position Masimo technology in real world use…
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- Cambridge ConsultantsCambridge
- Your role will focus on providing company-wide regulatory support to our project teams, spanning both medical and non-medical disciplines, as well as supporting…
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View similar jobs with this employerHologicCambridge CB4 0WN- Company pension
- Experience in the regulated medical device industry, ideally supporting product lifecycle and regulatory compliance activities.
- SThreeCambridge
- Knowledge of relevant regulatory frameworks and standards, including ISO 13485, IEC 62304, and Class III medical device regulations.
- SThreeCambridge
- Prior experience supporting medical device submissions or regulatory inspections.
- Understanding of Class III medical device regulatory requirements and product…
- Capgemini EngineeringCambridge
- We are seeking an experienced Product Assurance Manager to support a major space systems programme within a Space Systems Quality organization.
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- Capgemini EngineeringCambridge
- We are seeking an experienced Product Assurance Manager to support a major space systems programme within a Space Systems Quality organization.
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- GlaxoSmithKlineStevenage
- This role sits within Global Clinical Study Delivery (GCSD) as part of the Global Clinical Operations (GCO) function in GSK’s Research & Development (R&D)…
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R&D Quality Manager
Job details
Pay information not provided
Annual leave, Company pension
Full-time
Cambridge
Full job description
The Quality Manages complex projects or late phase projects and processes to support departmental portfolio, projects and objectives according to agreed timelines and standards.
Ensures that compliance with cGMP is maintained in Drug Delivery Device Development
Your Key Responsibilities:Your responsibilities include, but not limited to:
•
•
Competitive salary, Annual bonus, Pension scheme, Health insurance, 24 days annual leave, Flexible working arrangements, Employee recognition scheme, learning and development opportunities.
Why Sandoz?
Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human right of good health.
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!
Join us, help us make healthcare fairer and faster.
Commitment to Diversity& Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
#Sandoz
Ensures that compliance with cGMP is maintained in Drug Delivery Device Development
Your Key Responsibilities:Your responsibilities include, but not limited to:
•
- Quality responsible person for the assigned Design History File portfolio
- Support quality aspects of development projects and/or processes assigned to department and assure compliance with Medical devices as well as Combination product regulations, good pharmaceutical practices and Sandoz internal standards.
- Support quality problems and technical matters an ensure they are re-solved consistently and in accordance with global standards and policies.
- Release of medical devices and device components of combination products for clinical batch production Represent Quality Drug Delivery Device Development in initiatives and cross-divisional projects
- Perform or support inspections and audits as required Approval of Deviation and OOS/OOE and change Controls in Sandoz systems
- Approval in document management systems
- Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidance, SOPs etc.).
•
- Expert knowledge in Medical Device and Combination product regulations (EU MDR, FDA CFR Part 820 and Part 4, ISO 13485)
- Functional Breadth - Quality Management, Change Control and Audit Management
- Project Management Skills - Critical Negotiations, Influencing Skills and Collaboration across boundaries
- Excellent communication skills in English
Competitive salary, Annual bonus, Pension scheme, Health insurance, 24 days annual leave, Flexible working arrangements, Employee recognition scheme, learning and development opportunities.
Why Sandoz?
Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human right of good health.
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!
Join us, help us make healthcare fairer and faster.
Commitment to Diversity& Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
#Sandoz
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