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Project manager

Lenham
Bedfont Scientific Ltd
Project manager
€40,000 a year
Posted: 24 October
Offer description

Salary Range: £36,000 to £40,000 Location: Harrietsham, Kent

Application and Interviews
The job advert closes on 14th November 2025, with 1st stage telephone interviews and second stage face-to-face interviews scheduled to be held during the last two weeks of November 2025.

Hybrid Working Opportunity
This role is eligible for the hybrid working benefit, requiring the successful candidate to attend our Harrietsham office three days per week, with the flexibility to work from home up to two days a week once deemed competent to work independently and in line with the business needs. Applicants must be UK-based and live within a practical commutable distance of our office. Hybrid working is a benefit at Bedfont and not a contractual term.

The Story:
Established in 1976, Bedfont is an award-winning medical technology company based in Harrietsham, Kent. Its breath analysis medical devices are exported globally thanks to its network of carefully selected distributors.

The Challenge:
Healthcare is evolving and the market for breath analysis monitors is expanding. Bedfont are looking for hard-working, like-minded, and passionate individuals to join the Bedfont Family to help achieve its goal of innovating healthcare worldwide.

The Benefits:
25 days paid holiday plus bank holidays
Social events
Private medical insurance
Subsidised health checks
Well-being warriors
Well-being garden and room
Annual optical allowance
Cycle to work scheme
Pension scheme
Bonus scheme
Hybrid working
Employee Assistance Programme (EAP)
Rewards app
Referral bonus
Charity days
Home office setup allowance
Employee awards
Free on-site parking
Training & development opportunities
Free uniform
Subsidised Celler8 device
Subsidised kids club
Time in service annual leave bonus
Enhanced Maternity and Paternity Pay

Your Mission:
The Project Manager will lead projects end-to-enddefining scope, goals and deliverables in line with design-control procedures; building detailed plans and work packages; and aligning resources. They will coordinate stakeholders across Marketing, Sales, Clinical, R&D and Regulatory, run the stage-gate process and design reviews, and drive quality to Company standards. Day to day, they will track deliverables with appropriate tools, manage risks, oversee suppliers and any outsourced manufacturing for key projects, and ensure on-time, on-budget delivery to specification and customer/marketing requirements. The role includes providing clear status reports and recommendations to the Project Management team and wider stakeholders, anticipating and responding to change throughout execution.

Roles and Responsibilities:
Facilitate the definition of project scope, goals and deliverables in accordance with design control procedures.
Create and deliver detailed project plans and work packages to achieve each stage of the project and desired outcomes.
Manage and co-ordinate project resource allocation in alignment with O/A Programme.
Work closely with relevant stakeholders to ensure effective and efficient implementation of the project(s).
Ensure product quality and Company standards are met.
Engage in product & project risk meetings.
Co-ordinate design reviews to ensure product is designed and engineered to specification.
Manage stage gate process by coordinating internal stakeholders including Marketing, Sales, Clinical, R&D, and Regulatory.
Coordinate departmental functions to ensure the final product is delivered on time, within budget and in line with customer and marketing requirements for performance and quality.
Track project deliverables using appropriate tools.
Manage day-to-day operational aspects of the project(s).
Co-ordinate clients and suppliers on outsourced manufacturing processes, goods and services as required for the key projects.
Report to the Project Manager (Manager) on project plans and timescales and make appropriate recommendations.
Submit project status reports to all stakeholders and anticipate and react to change.

Qualifications:
Qualification in Prince 2 Project Management or equivalent
Minimum of 2 years Project Management experience
Experience in a medical device or hardware manufacturing environment desirable
Exposure to Wrike desirable

Key Skills & Competencies:
Clear and confident communicator (written & verbal), able to convey complex ideas simply
Ability to influence and work with stakeholders of all levels
Negotiation & facilitation skills to resolve priorities and dependencies
Critical thinking & structured problem-solving and able to drive decisions with data
Strong knowledge of project and planning tools/software as well as collaboration suites such as M365.
High attention to detail with sound commercial awareness
Decisive with good judgement, knowing when to escalate

In addition, employees may be required to undertake other duties as may reasonably be required of them. In these circumstances training will be given where it is considered.

Bedfont Scientific Ltd. does not and will not discriminate in the recruitment or managing of staff on the basis of race, colour, religion, gender, age, disability, marital status, sexual orientation and more. We are an equal opportunity employer and Bedfont regards every employee as a member of the Bedfont family and is committed to providing a fair, safe, diverse and welcoming atmosphere. Our application process has been designed so that everyone is able to demonstrate their skills and how they meet the criteria required for the job advertised. All successful candidates will be subject to a digital ID and DBS check.

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