Project Manager
- Recruiter
- Confidential
- Location
-
Stirling
StirlingUnited Kingdom
- Salary
- Competitive
- Posted
- 05 Oct 2020
- Closes
- 02 Nov 2020
- Job Title
- Project Manager
- Category
- Information Technology
- Contract Type
- Permanent
- Hours
- Full Time
Project Manager
LumiraDx is a medical technology company developing, manufacturing and marketing smart connected diagnostics and diagnostic–led care solutions. Founded in 2014 by entrepreneurs with a successful track record in building and scaling medical diagnostics and health IT businesses, the company has major operations in the UK and the USA, and is supported by a global sales network, LumiraDx currently has over 700 employees worldwide.
We have recently launched the innovative LumiraDx Platform, and are looking for proactive, experienced, focused and enthusiastic individuals who can make a significant contribution to the continued growth and success of our dynamic and forward–looking company.
Scope of the role
The Project Manager will lead various project teams with a high–level degree interaction with other functions within LumiraDx. The main responsibility is to ensure that assigned projects in the design review process are completed on schedule and meet quality objectives. This individual develops detailed project plans, sets schedules/timelines, secures resources, provides status reports, and ensures all project documentation is completed in accordance with LumiraDx's Quality System.
Purpose of the role
This role will be working in our global disease portfolio with cross–functional teams, leading and driving assay development projects from concept to post–launch phase.
Key areas of responsibility
* Lead Assay Development Projects, whilst employing a business–driven mindset
* Develops full scale project plans, including tasks, scheduling, timelines, milestones, resources, budget.
* Maintains plans, schedules, and timelines updating, as necessary.
* Ensures alignment & mutual commitment between the Project & Functions
* Manages Project risk analysis, risk mitigation plans within the Project team: initiation, follow–up & reporting
* Manages Project documentation in accordance with applicable regulations and company policies and procedures
* Define, measure, and communicate project progress to leadership functions.
* Serves as chairperson for design and technical reviews.
Position Requirements
* Degree education
* ??? 2 years of direct work experience in medical device instrument, biotechnology, or life science industry.
* Project Management experience in various aspects of product development and sustaining execution and product launch.
* Experience in Quality System Regulations (QSR) 21 CFR 820; Design Control: ISO 13485:2003, FDA regulations.
* Project management qualification e. g. PMP??, PRINCE2, APMP, preferable
* Working in a global environment. Must be able to accommodate flexible working hours.
* Experience in organizing own work to deliver projects to meet quality, budget, and timeline requirements
* Skills in MS Office packages (e.g. Excel, Word, Outlook, PowerPoint, Project, Gantt Charts)
* Proactive, cross–functional, and enthusiastic team player with an ability to work flexibly, under pressure and to tight timelines
* Excellent organization, negotiation, and interpersonal skills, with ability to communicate effectively
* Business–driven approach
* Drives effective decision making
* Concern for regulation and quality best practice
* Develops and applies skills and knowledge
Please note, if you wish to submit an application for this role, please consider the following information This vacancy is open to internal and external candidates. If you are an internal candidate, please notify your line manager before you submit your application. If you're successful, you may be subject to all or some of the LumiraDx standard pre–employment checks.
Criminal records data is processed as part of our recruitment and selection processes and, where necessary, in the course of employment, we verify that candidates are suitable for employment or continued employment to comply with legal and regulatory obligations to which the company is subject.
LumiraDx place a high level of importance on its responsibilities for information security and privacy and have put in place an information security management system to ensure that the company and its staff maintain the highest standards with respect to data protection and information security. All staff are responsible for information security and therefore must understand and comply with the Company information security policies, procedures and guidance
LumiraDx is a medical technology company developing, manufacturing and marketing smart connected diagnostics and diagnostic–led care solutions. Founded in 2014 by entrepreneurs with a successful track record in building and scaling medical diagnostics and health IT businesses, the company has major operations in the UK and the USA, and is supported by a global sales network, LumiraDx currently has over 700 employees worldwide.
We have recently launched the innovative LumiraDx Platform, and are looking for proactive, experienced, focused and enthusiastic individuals who can make a significant contribution to the continued growth and success of our dynamic and forward–looking company.
Scope of the role
The Project Manager will lead various project teams with a high–level degree interaction with other functions within LumiraDx. The main responsibility is to ensure that assigned projects in the design review process are completed on schedule and meet quality objectives. This individual develops detailed project plans, sets schedules/timelines, secures resources, provides status reports, and ensures all project documentation is completed in accordance with LumiraDx's Quality System.
Purpose of the role
This role will be working in our global disease portfolio with cross–functional teams, leading and driving assay development projects from concept to post–launch phase.
Key areas of responsibility
* Lead Assay Development Projects, whilst employing a business–driven mindset
* Develops full scale project plans, including tasks, scheduling, timelines, milestones, resources, budget.
* Maintains plans, schedules, and timelines updating, as necessary.
* Ensures alignment & mutual commitment between the Project & Functions
* Manages Project risk analysis, risk mitigation plans within the Project team: initiation, follow–up & reporting
* Manages Project documentation in accordance with applicable regulations and company policies and procedures
* Define, measure, and communicate project progress to leadership functions.
* Serves as chairperson for design and technical reviews.
Position Requirements
* Degree education
* ??? 2 years of direct work experience in medical device instrument, biotechnology, or life science industry.
* Project Management experience in various aspects of product development and sustaining execution and product launch.
* Experience in Quality System Regulations (QSR) 21 CFR 820; Design Control: ISO 13485:2003, FDA regulations.
* Project management qualification e. g. PMP??, PRINCE2, APMP, preferable
* Working in a global environment. Must be able to accommodate flexible working hours.
* Experience in organizing own work to deliver projects to meet quality, budget, and timeline requirements
* Skills in MS Office packages (e.g. Excel, Word, Outlook, PowerPoint, Project, Gantt Charts)
* Proactive, cross–functional, and enthusiastic team player with an ability to work flexibly, under pressure and to tight timelines
* Excellent organization, negotiation, and interpersonal skills, with ability to communicate effectively
* Business–driven approach
* Drives effective decision making
* Concern for regulation and quality best practice
* Develops and applies skills and knowledge
Please note, if you wish to submit an application for this role, please consider the following information This vacancy is open to internal and external candidates. If you are an internal candidate, please notify your line manager before you submit your application. If you're successful, you may be subject to all or some of the LumiraDx standard pre–employment checks.
Criminal records data is processed as part of our recruitment and selection processes and, where necessary, in the course of employment, we verify that candidates are suitable for employment or continued employment to comply with legal and regulatory obligations to which the company is subject.
LumiraDx place a high level of importance on its responsibilities for information security and privacy and have put in place an information security management system to ensure that the company and its staff maintain the highest standards with respect to data protection and information security. All staff are responsible for information security and therefore must understand and comply with the Company information security policies, procedures and guidance
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