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New Product Development Specialist, Winsford
Client: Advanced Medical Solutions
Location: Winsford, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Views: 1
Posted: 22.08.2025
Expiry Date: 06.10.2025
Job Description:
Who are Advanced Medical Solutions?
AMS is a world-leading independent developer and manufacturer of innovative tissue-healing technology, focused on quality outcomes for patients and value for payers. AMS offers a wide range of surgical products including tissue adhesives, sutures, haemostats, internal fixation devices, and internal sealants under various brands. AMS also supplies wound care dressings such as silver alginates, foams, and other products through its ActivHeal brand and white label. Established in 1991, AMS has over 1,500 employees and operates R&D hubs across multiple countries.
AMS provides equal employment opportunities and values diversity, ensuring no discrimination based on gender, race, age, nationality, disability, or other protected characteristics.
Job details
Responsible for supporting the Woundcare category, working with the Commercial Team to explore business opportunities and develop products for new and existing customers.
What the role involves:
* Identify and develop innovative intermediate and finished product developments (NPD), generating documentation in accordance with AMS procedures, GLP, GDP, and regulations.
* Collaborate with the Commercial Team and other departments to assess new opportunities and develop Business Cases.
* Build relationships with existing and new suppliers.
* Serve as a technical point of contact for customers and new business prospects.
* Project manage AMS Stafford NPD business opportunities.
* Participate in Winsford NPD projects as R&D stakeholder.
* Develop prototypes based on customer insights and present ideas to clients.
* Develop and validate methods for manufacturing and characterizing NPDs.
* Author technical protocols and reports, planning sample testing and creation.
* Apply statistical methods for evaluation.
* Plan pilot and mainline trials, manage responsibilities and materials.
* Define new product construction and develop concepts to drive growth.
* Design stability studies for shelf-life determination.
* Monitor and report on technical KPIs.
* Participate in risk evaluations using tools like PFMEA/DFMEA.
* Hold a BS Degree or equivalent in a scientific discipline or have at least 3 years of experience in a similar role within medical device or pharmaceutical industries.
What we’re looking for:
* BS Degree or equivalent in scientific discipline or relevant experience.
* Knowledge of applicable Quality System Regulations and ISO standards.
* Understanding of QA, Manufacturing, Validation, Change Control, and Design Control processes.
* Proficiency in statistics, sampling plans, and analysis.
* Experience with analytical methods, equipment, and validations.
* Ability to plan, execute, and solve moderate to complex problems independently.
* Good communication skills for report writing and interaction with staff and clients.
* Capability to manage multiple projects.
* Innovative mindset with NPD experience.
* Computer literacy in Word, PowerPoint, and Excel for reporting and data analysis.
Other: The role is expected to be approximately 50% on-site and 50% remote.
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