Job Description
R&D Project Manager – 12 month FTC
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, marketed under brands such as LiquiBand, RESORBA, LiquiBandFix8, LIQUIFIX, Peters Surgical, Ifabond, Vitalitec, and Seal-G. The company also supplies wound care dressings like silver alginates, alginates, and foams through its ActivHeal brand, as well as white label products. Since 2019, AMS has made seven acquisitions, expanding its portfolio and capabilities. Its products are manufactured across various countries including the UK, Germany, France, Netherlands, Thailand, India, Czech Republic, and Israel, and are sold globally through a network of partners and direct sales teams. AMS has R&D hubs in the UK, Ireland, Germany, France, and Israel. Established in 1991, the group employs over 1,500 staff. For more information, see www.admedsol.com.
AMS is committed to equal employment opportunities, valuing diversity and encouraging applications from all qualified individuals, regardless of protected characteristics.
Job Details
The role involves delivering R&D projects aligned with the company's business plan, ensuring compliance with medical device and FDA procedures. The Project Manager will support Sales & Marketing, Operations, Quality, and Regulatory Affairs in product commercialization, manufacturing, and maintenance.
What will this role involve?
* Planning, controlling, and monitoring complex product development projects.
* Leading cross-location project teams to achieve objectives.
* Evaluating project proposals, developing project mandates, and coordinating stakeholder engagement, including resource allocation and communication management.
* Following the company's Product Development Process and presenting at key decision points.
* Overseeing Design Control activities, including document approval processes.
* Managing Risk processes for new product development, ensuring ISO 14971 compliance.
* Keeping stakeholders informed of progress and issues, reporting via the NPD process.
* Managing project risks and conflicts proactively.
* Building strong relationships and coordinating activities with internal and external partners, vendors, and test houses.
* Applying engineering and scientific principles to the design, development, and manufacture of medical devices.
* Ensuring compliance with company and quality procedures, GMP, GLP, and Health & Safety standards.
* Performing additional tasks as requested by management.
What we're looking for?
* Understanding of project work and deadline adherence.
* Knowledge of product development procedures and processes.
* Familiarity with GMP, ISO 13485, EN 4600, and FDA quality systems.
* Understanding of test procedures.
* Strong communication and organizational skills.
* Minimum educated to A-level in a science or engineering discipline.
* Attention to detail and analytical mindset.
* Proficiency with PC systems and relevant software.
* Ability to analyze test results and report findings.
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