Join to apply for the Senior Scientist (Fixed-Term) role at Convatec
About Convatec: Convatec is a global medical products and technologies company focused on solutions for chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. The company operates in around 90 countries with over 10,000 colleagues and revenues over $2 billion (2024).
Overview
As a Senior Scientist you will perform analytical testing on existing and new medical devices, skin care products and raw materials according to pre-determined protocols, SOPs, OCIs and TDs in support of product claims. You will also support business units in the design, development, and validation of new analytical test methods upon request.
Responsibilities
* Maintain compliance to ISO13485 and ISO9001 standards in accordance with GLP/GMP compliant procedures.
* Analyze, document, interpret, and report laboratory data to GMP/GLP standards.
* Collate and report laboratory data in technical reports.
* Design, develop, and validate new analytical methods for new products and/or techniques.
* Maintain, calibrate, document and update quality records for the Analytical Laboratory.
* Support planned and ad-hoc analytical testing and test method development; support laboratory tasks as required.
* Write quality documentation such as Change Control Records, Non-Conformances, and Out of Specifications where appropriate.
* Perform laboratory/OOS investigations with supervision, applying problem-solving and troubleshooting for future improvements.
* Ensure the Analytical labs are maintained as a safe working environment, raising near misses where needed.
* Serve as technical expert in laboratory equipment (e.g., HPLC) and related instruments (e.g., balances, pipettes, FTIR, ICP-MS).
* Engage in structural elucidation of unknown chemical structures from complex mixtures using high resolution Mass Spectrometry and other techniques.
* Autonomously design and perform laboratory research, investigations and method development.
* Write SOPs, OCIs and TDs through to submission into the Electronic Data Management System for approval.
* Use basic and advanced software packages for ordering, data collection, analysis, and statistical manipulation (e.g., Word, Excel, SAP; Waters Empower, ChemStation, MassHunter, Minitab).
* Monitor stock levels of laboratory consumables and reagents and request reorders while improving stock management.
* Perform technical data checking for analytical test methods and technical approval checking for reports from the Analytical function.
* Provide support for other R&D groups with laboratory testing as required.
* Coordinate with external vendors for service contracts as well as maintenance, servicing, and calibration of equipment.
* Train new and inexperienced staff in test methods and equipment as indicated in training records.
* Support internal and external audits with timely information where required.
* Contribute to improvements in Analytical processes and Lean/6S initiatives; update test and operating procedures as needed.
Skills & Experience
* 3-4 years’ experience in Medical Device/Pharmaceutical Industry in an R&D/product development role (preferable).
* Good working knowledge of laboratory Health and Safety practices.
* Competent in advanced chemistry and laboratory techniques.
* Competent in adhering to SOPs, OCIs and TDs; capable of method validation for new products and raw materials.
* Basic experience with computerized data management systems.
* Good working knowledge of Microsoft Office (Word, Excel).
* Understanding of FDA and European Regulations (ICH), Quality Systems and GMP Guidelines.
* Disciplined approach to achieving group objectives and teamwork.
Working Conditions
* Laboratory environment with exposure to chemicals, reagents, and solvents.
* Ability to dispose of chemicals and reagents per site and environmental procedures.
* Ability to adapt to changes in priority and workload; balance multiple priorities to meet objectives.
* Use of VDU equipment.
Important notices
Beware of scams online or from individuals claiming to represent Convatec. A formal recruitment process is required for all 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, contact careers@Convatec.com.
Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants. No one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, disability, sexual orientation, gender identity, military status, or any other basis prohibited by law.
Notice to Agencies
Convatec is not accepting unsolicited resumes from agencies or search firms for this job posting. Resumes submitted to Convatec employees by third parties without a valid written agreement may become the property of Convatec. No fee will be paid for unsolicited referrals. Thank you.
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