Microbiology Manager

SRG

Wales

On-site

GBP 45,000 - 65,000

Full time

14 days+

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Job summary

A prominent company in medical products and technologies is seeking a Microbiology Manager. This role requires overseeing laboratory activities, ensuring compliance with industry standards, and leading the microbiology team. Ideal candidates will have substantial experience in the medical device sector, with strong skills in microbiology management and team leadership.

Qualifications

7+ years’ experience in Medical Device or Pharmaceutical Industry.
Experience with FDA 510k submissions.
Strong background in microbiology and laboratory management.

Responsibilities

Oversee microbiology laboratory activities and manage the team.
Ensure compliance with quality and safety standards.
Manage microbiology testing programs and validation activities.

Skills

Microbiology

Team Leadership

Problem Solving

Communication

Organisational Skills

Strategic Thinking

Education

Degree in biological science

Tools

LIMS

Microsoft Office

Job description

SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care.

Our client is seeking a Microbiology Manager to join their team.

The microbiology manager is responsible for the oversight of microbiology laboratory activities and for management of the microbiology team. This role involves close collaboration with new product development project teams to drive the successful development of new products, and maintaining quality, compliance and safety standards within all microbiology team activities.

Key Responsibilities

To act as a technical expert on behalf of the organisation by providing advice, guidance, and expertise on microbiological issues.
Actively manage the microbiology laboratory team, including effective engagement, communication, recruitment, and employee development.
Responsible for managing the microbiology testing programme. Ensure all microbiological testing, methods and validation exercises reflect applicable regulations/guidelines and meet industry best practice.
Accountable for meeting targeted KPI’s and monitoring team performance; maintain and update all assigned systems and databases. Provides regular management reports as required.
Responsible for microbiology test method validation and equipment validation requirements in accordance with company procedures.
To manage and ensure appropriate allocation of laboratory resources and drive on-time completion of team activities.
Accountable for software validation activities for the deployment of microbiology laboratory equipment software packages.
Accountable for Microbiology Laboratory safety, including the timely preparation and approval of all required laboratory safety deliverables.
Lead/manage continuous improvement initiatives within microbiology systems.
To lead/manage microbiology laboratory related non-conformances, CAPA’s, planned deviations, change controls, OOS’s as required, ensuring corrective actions are fully implemented to address root causes etc.
Perform other activities as and when required to support laboratory operations.

Skills & Experience

Preferably 7+ years’ experience working in the Medical Device / Pharmaceutical Industry within a R&D/product development role.
Experience with FDA 510k submissions and test methods for microbiological claims.
Strong background in microbiology, significant experience, track record and knowledge within Microbiology or a Laboratory Management environment.
LIMS experience nice to have
Method Validation nice to have
Med device nice to have
A drive for excellence and high attention to detail.
Ability to lead, motivate, develop, and influence a team.
Competent to provide technical support and advice to other functions and franchises; serves on various teams as a functional leader.
Strategic thinking capabilities evidenced by successful delivery of projects in a previous laboratory role.
Strong organisational skills and the ability to manage business complexity and multiple priorities at one time.
Ability to network internally and externally and stay engaged via industry best practices and standards.
Good interpersonal skills and ability to form effective working relationships

Qualifications/Education:

Degree level in a biological science discipline, preferably in microbiology.
Working knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO13485:2016, ISO9001:2015, FDA 21 CFR part 820) and GMP Guidelines and Regulations.
Possess a flair for problem solving, identifying inefficiencies and implementing solutions.
Microsoft Office skills are essential.
Working knowledge of statistics and software packages are preferable.

Seniority level