Job Description

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 around 10,000 colleagues, we provide our products and services in almost 100 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. Group revenues in 2022 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com

Job Summary

Our successful Stability Scientist will be tasked with performing physical and analytical stability testing on existing and new medical devices and skin care products according to pre-determined stability study protocols, SOPs, OCIs and TDs in support of product shelf-life and product labelling.

Key Duties and Responsibilities

• Analysing, documenting, interpreting, and reporting laboratory data for stability studies to GMP/GLP standards.
• Support maintenance, calibration, documentation and updating quality records for Stability equipment.
• Maintain compliance to ISO13485 & ISO9001 standards in accordance with GLP/GMP compliant procedures.
• Provide technical knowledge to some stability studies with support from Senior Scientist.
• Experience with a wide range of analytical equipment such as balances and pipettes through to HPLC and ICP-MS.
• Write shelf-life plans/reports and stability protocols/reports with some support from Senior Scientist/Specialist.
• Performs Lab/OOS investigations with some supervision incorporating problem-solving and troubleshooting for future improvements.
• Identify when laboratory consumables, chemicals and reagents are low and request for reorder whilst continuously improving stock management.
• Perform the drafting of stability documentation such as protocols and reports.
• Write Quality documentation such as Change Control Records, Non-Conformances, and Out of Specifications.
• Ensure the Stability labs are maintained as a safe working environment, raising near misses where needed.
• Support planned and ad-hoc stability sample set-downs, pull requests and support laboratory tasks as and when required.
• Collation of stability data, including physical data retrieval, for stability/technical reports.
• Assist in the storage and retrieval of stability samples.
• Support any on-site maintenance, service and calibration activities performed by external vendors.
• Supports and provides information for internal and external audits where required in a timely manner.
• Coordination and organisation of studies from concept to completion including sample retrieval, as advised by senior team members.
• Suggest appropriate accelerated and real-time aging programmes that are suitable for the study in concept.
• Actively execute improvement ideas (Lean/6S) for the Stability laboratories and suite.
• Support improvements to current stability processes including updates to test and operating procedures.
• Train new and inexperienced members of staff in test procedures and related equipment calibration/use.

About You

• B.Sc. or equivalent in a scientific discipline (e.g., Chemistry, Biology).
• Preferably 1-2 years\xe2\x80\x99 experience working in Medical Device/Pharmaceutical Industry within an R&D/product development role.
• Ability to react and respond positively to changes in priority and workload.
• Competent in following and adhering to pre-determined stability study protocols, SOPs, OCIs and TDs.

• Basic experience in the utilisation of computerised systems to manage data and information.
• An active team player disciplined in adhering to group objectives including taking an active role in team collaborative activities.
• Good working knowledge of Microsoft Office - specifically Word and Excel.
• Understanding of compliance with FDA and European Regulations (ICH), Quality Systems and GMP Guidelines.
• Proactive and positive mindset with an attitude that is open to change to embrace new ways of working and improvements.
• Competent in the disposal of chemicals, reagents and solvents in accordance to site and environmental procedures.

Working Conditions

• Working in a laboratory environment with exposure to chemicals, reagents, and solvents.
• Working with various storage chambers (freezer, fridge, incubators etc.) for sample retrieval and deposit.
• Understanding of the role of stability testing within the product development lifecycle.
• Ability to adapt to a changing environment and balance multiple, competing priorities to meet objectives.
• Good working knowledge of laboratory Health and Safety Practices.
• Use of VDU equipment.

Our transformation will change your career. For good. You\'ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you\'ll be supported to bring them to life. There\'ll be challenges. But stretch yourself and embrace the opportunities, and you could make your biggest impact yet.

This is stepping outside of your comfort zone.

This is work that\'ll move you.

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Beware of scams online or from individuals claiming to represent Convatec

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\xe2\x80\x99re unsure, please contact us at .

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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If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

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