Scientist II - 1 year contract

About Convatec

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

Convatec has announced a major milestone in our R&D journey and commitment to our vision of pioneering trusted medical solutions to improve the lives we touch. We have unveiled plans to relocate the majority of our UK-based research and development (R&D) activities from Deeside to Manchester from late 2027/early 2028, alongside a significant expansion of our facilities in Boston. 
 
An exciting future in Manchester
The new, planned Manchester facility has the potential to be a major R&D hub in our global network which will initially function as the company’s global testing laboratories, with cutting-edge analytical R&D capabilities including quality control and materials, regulatory functions, and health innovation, positioning Convatec at the forefront of medical technology development. Our new state-of-the-art facilities will also strengthen our collaboration with Manchester’s vibrant life sciences ecosystem, which includes leading universities, hospitals, and research institutions.

Position Overview:

Scientist II in the microbiology laboratory in the Global Testing Laboratories. Responsible for providing scientific and technical support to the development of new products. This includes method development, validation and testing. Ensures that all work performed in the microbiology lab conforms to internal procedures, reflects applicable regulations/guidelines and meets industry best practice.

Key Responsibilities:

• Working within a controlled ISO13485 laboratory quality system and in accordance with GLP/GMP compliant procedures.
• Perform routine microbiological tests to support the development of new medical device products.
• Development and validation of new microbiological assays.
• Accurate recording and analysis of laboratory data in accordance with good documentation practices.
• Writes validation protocols, reports and technical documents.
• Writes laboratory test methods/procedural revisions.
• To perform routine review of laboratory bench books/data, logbooks, equipment records; verifies/validates spreadsheets.
• Training of staff in microbial techniques and procedures.
• Responsible for standard laboratory routines, equipment calibration, maintenance, replenishment etc.
• Preparation and maintenance of microbial stock cultures.
• Ensure compliance with quality control and laboratory processes and procedures; write non-conformance and change control reports 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:

• An understanding of the role of microbiological testing within the product development process, particularly as it applies to the development of Medical Devices/Pharmaceuticals.
• Good microbiological and problem-solving skills and demonstrates an understanding of the steps involved in initiating and completing a variety of microbiological tasks to support key R&D projects.
• Ability to execute experiments in an accurate, effective and timely manner, reporting progress to senior microbiology staff.
• Excellent oral and written communication skills.
• Ability to use own initiative whilst working as part of a team.
• Ability to handle multiple tasks simultaneously.
• Demonstrates an ability to handle multiple tasks simultaneously.
• Proactive and flexible in adapting to a changing environment and ability to balance multiple, competing priorities to meet objectives.
• Highly motivated, possessing excellent personal attributes as well as being a flexible team member willing to take on a wide variety of tasks.
• A practical, methodical, and flexible approach to working.
• Ability to work effectively and communicate in cross-functional teams, building co-operative working relationships.

Qualifications/Education:

• Degree qualified, ideally in Microbiology, Biology or a similar related discipline.
• Experience in a working microbiology laboratory environment, preferably within a Medical Device/Pharmaceutical Industry is desirable.
• 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, particularly Word and Excel.

Working Conditions

• Laboratory/Office Environment
• Working in a laboratory environment with exposure to biological agents, chemicals and reagents.

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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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.

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