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Team Lead - Laboratory Services

Rhian_Convatec

Wales

On-site

GBP 45,000 - 65,000

Full time

2 days ago
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Job summary

A leading medical products company in the UK seeks a Team Lead for Laboratory Services. The role includes managing microbiology laboratory operations, supervising staff, and ensuring regulatory compliance. Candidates should have over 5 years of microbiology experience and a degree in a relevant field. The position is based onsite in Deeside, offering a chance to make a meaningful impact in medical solutions.

Qualifications

  • 5+ years of Microbiology Laboratory work experience.
  • Background in microbiology with a track record in a laboratory environment.
  • Knowledge of FDA and European regulations.

Responsibilities

  • Manage daily operations of the microbiology laboratory.
  • Supervise microbiology staff and ensure compliance with regulations.
  • Conduct training and oversee laboratory testing schedules.

Skills

Microbiology Laboratory experience
Analytical and problem-solving skills
SOP writing skills
Microsoft Office skills
Supervisory experience

Education

Degree in Microbiology, Biology or related discipline

Job description

About Us
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com

About the role:

Team Lead – Laboratory Services is responsible for the daily technical operation of the microbiology laboratory, supervising a team of microbiology staff, overseeing the laboratory testing schedule and ensuring all microbiological testing, processes, methods, and validation exercises conform to internal procedures, reflect applicable regulations/guidelines and meet industry best practice.

Your key duties and responsibilities:

  • Working within a controlled ISO13485 laboratory quality system and in accordance with GLP/GMP compliant procedures.
  • Supervise a team of 3-6 microbiology staff.
  • Ensures microbiology lab staff are trained and proficient at their assigned tasks and follow established standard procedures for the tasks they are performing.
  • Conducts General Laboratory Compliance Awareness training as part of new starter inductions; ensures lab compliance with applicable cGMP regulations and SOP’s.
  • Takes responsibility for the daily technical operation of the microbiology laboratory.
  • Oversees the laboratory testing schedule and ensures all microbiological testing, processes, methods, and validation exercises conform to internal procedures, reflect applicable regulations/guidelines and meet industry best practice.
  • Responsible for prioritisation of tasks to ensure deadlines are met in accordance with testing schedules.
  • Represents the Microbiology Lab as a functional lead on various teams.
  • Deputize in the absence of a laboratory manager; represents the microbiology laboratory during internal and external audits.
  • To troubleshoot issues as they occur in the microbiology laboratory and manage deficiencies, OOS’s, non-conformances and failures with respect to equipment, procedure, processes and test methods within the laboratory.
  • Ensure all laboratory instrumentation and equipment are appropriately calibrated in accordance with regulatory requirements and calibration schedules.
  • Ensures microbiology equipment is fully qualified (IQ/OQ/PQ) to expected standards; supports software validation activities as and when required.
  • Perform detailed laboratory investigations to determine the root cause for atypical and out of specification results, apply corrective and preventive actions and concise report investigations.
  • Write COSHH and risk assessments for laboratory procedures.

Skills & Experience:

  • 5+ years of Microbiology Laboratory work experience responsibilities.
  • Working knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (preferable ISO13485:2016, ISO9001:2015, FDA 21 CFR part 820 or equivalent), GMP and GDP.
  • Working knowledge and experience of microbiology related pharmacopeial/ISO standards.
  • Experience of supervising staff in a laboratory setting.
  • Background in microbiology; experience, track record and knowledge within microbiology or a laboratory environment.
  • Demonstrated excellent analytical and problem-solving skills and ability to interpret data from a variety of sources.
  • Excellent SOP, investigation, protocol, and technical report writing skills.
  • Microsoft Office skills are essential.
  • Ability to work effectively and communicate in cross-functional teams, building co-operative working relationships.
  • Highly motivated, possessing excellent personal attributes as well as being a flexible team member willing to take on a wide variety of tasks.

Qualifications/Education:

  • Degree qualified, ideally in Microbiology, Biology or a similar related discipline.
  • Knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO13485:2016, FDA 21 CFR part 820) and GMP Guidelines and Regulations is desirable.
  • Good working knowledge of Microsoft Office, specifically Word and Excel.

Travel Requirements:

  • Position may involve minimal travel, between 1-5 days per year.

Working Conditions:

  • This role may be based in the Deeside with an onsite working structure.
  • Laboratory/Office Environment
  • Working in a laboratory environment with exposure to biological agents, chemicals and reagents.

Special Factors:

  • Exposure to biological agents (Hazard Group 1 and 2).

Ready to join us?

At Convatec, we’re pioneering trusted medical solutions to improve the lives we touch. If you’re ready to make a real impact, apply today and help us bring our Forever Caring promise to life.

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A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.

Equal opportunities

Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

Notice to Agency and Search Firm Representatives

Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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