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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 has a wide range of surgical products including tissue adhesives, sutures, haemostats, internal fixation devices and internal sealants, which it markets under its brands LiquiBand®, RESORBA®, LiquiBandFix8®, LIQUIFIX™, Peters Surgical, Ifabond, Vitalitec and Seal-G®. AMS also supplies wound care dressings such as silver alginates, alginates, and foams through its ActivHeal® brand as well as under white label. Since 2019, the Group has made seven acquisitions: Sealantis, an Israeli developer of innovative internal sealants, Biomatlante, a French developer and manufacturer of surgical biomaterials, Raleigh, a leading UK coater and converter of woundcare and bio-diagnostics materials, AFS Medical, an Austrian specialist surgical business, Connexicon, an Irish tissue adhesives specialist, Syntacoll a German specialist in collagen-based absorbable surgical implants and Peters Surgical a global provider of specialty surgical sutures, mechanical haemostasis and internal cyanoacrylate devices. AMS's products, manufactured in the UK, Germany, France, the Netherlands, Thailand, India, the Czech Republic and Israel, are sold globally via a network of multinational or regional partners and distributors, as well as via AMS's own direct sales forces in the UK, Germany, Austria, France, Poland, Benelux, India, the Czech Republic and Russia. The Group has R&D innovation hubs in the UK, Ireland, Germany, France and Israel. Established in 1991, the Group has more than 1,500 employees. For more information, please see ___ AMS provides equal employment opportunities for all applicants. We highly value and encourage diversity across our workforce meaning that no one will be discriminated against because of their gender, race, age, nationality, disability, or any other protected characteristic as prohibited by law. What will this role involve? • Planning, controlling and monitoring technically complex R&D product development projects., • Project-related leadership of multifunctional cross-location teams to achieve the project goals., • Participation in the evaluation of the project proposal, the development of the project mandate and the identification of stakeholders including the co-ordination of resource allocation with line managers and clients and be responsible for communication management., • To follow the company’s Product Development Process and present at key decision points to business unit management team and Project Review Board., • To oversee Design Control activities, including ensuring appropriate document approval., • To oversee the Risk Management process for new product development and life cycle management projects, ensuring compliance to ISO 14971., • Keep all stakeholders informed of progress and issues. Reporting project status via the New Product Development Process (NPD process)., • Active management of project risks, issues and conflicts., • To form strong relationships and coordinate activities with internal and external customers, including external business partners, vendors, contractors and test houses., • To apply comprehensive and skilled knowledge of engineering/ scientific principles to the design, development and manufacture of medical devices., • The jobholder is responsible to follow company and quality procedures and maintain training records, including ensuring compliance with relevant GMP, GLP, Health & Safety standards., • To perform all reasonable tasks requested of them by their manager What we're looking for? • In-depth knowledge and understanding of projects work and adherence to deadlines, with proficiency in both waterfall and Agile methodologies., • Proficient knowledge and understanding of Medical Device product development procedures and processes., • Proficient knowledge of GMP/ISO13485/European MDR (EU 2017/745)/EN4600/FDA Quality System Regulation., • Proficient knowledge of Risk Management - ISO 14971., • An understanding of submission types: CE-marking pathways, FDA 510(k)/PMA, pre-sub/pre-IDE meetings, labelling, and regulatory timelines., • Cross-functional leadership: Skill in coordinating across R&D, regulatory, quality, clinical, supply chain, manufacturing, marketing, and legal teams., • Empathy, adaptability, active listening, and anticipation of user needs are indispensable., • Organization, Reporting & Communication: Using rigorous planning, risk logs, stakeholder alignment, precise status updates, and escalation strategies. Clear communication with technical and non‑technical audiences alike., • Thorough understanding of test procedures., • Educated to degree level in a science of engineering discipline as a minimum., • Attention to detail and analytically minded., • Familiarity with PC Systems and appropriate software, including Microsoft Project.

We’re working with an international law firm on a short-term document review project starting shortly, and they are looking to assemble a team of experienced document review paralegals. Previous involvement in large-scale or complex document reviews. This is a great opportunity for paralegals who

A leading law firm in the UK is seeking an experienced Associate for their Document Review team. The ideal candidate will oversee document review projects, manage a team of paralegals, and handle complex inquiries.

An international law firm is seeking experienced document review paralegals for a short-term, fully remote project in Greater London. The role entails conducting document reviews using Relativity, focusing on accuracy and efficiency while meeting tight deadlines. Candidates should have a solid under

One of our clients, a leading London law firm, are looking for four paralegals to join them on a 6/7 week document review project and review a large set of documents in order to help identify relevant documents which may be helpful to support a commercial arbitration filing. It is essential that you

A leading recruitment agency is seeking Litigation Paralegals for a document review project related to a significant international dispute. The ideal candidates should have completed their LPC and possess document review or litigation experience.

A leading legal services provider in London is seeking Paralegals fluent in Italian for a document review project on a full-time, temporary basis.

A top tier law firm in London is seeking a Portuguese Document Review Paralegal to review and analyze documents with efficiency. The role includes translating documents between Portuguese and English and preparing court documents. The ideal candidate must be fluent in both languages, have experience

A leading law firm in London is seeking a Temporary Paralegal to assist with a 6/7 week document review project. You will be responsible for reviewing documents to identify relevant materials for a commercial arbitration filing.

Portuguese Document Review Paralegal. Review and analyse documents in Portuguese with accuracy and efficiency. Document Review on eDiscovery platforms such as Relativity.

The role would particularly suit a Paralegal who has ideally completed the LPC and has some document review or Litigation experience. Competitive hourly document review rates will be paid for this role. Document Review - Litigation Paralegal.

German Document Review Paralegal for a top tier law firm in London. German Document Review Paralegal. Review and analyse documents in German with accuracy and efficiency.

Support other managers in the Document Review Team on other workflows outside of eDiscovery and document review. At TLT, our Document Review & Collation team is made up of a combination of qualified resource and Paralegals who support both contentious and non-contentious fee earners from across the

An international legal consultancy is seeking a team of French-speaking paralegals to assist with an urgent document review project starting ASAP. The role involves conducting document reviews on litigation matters and requires candidates to have a law degree and experience using Relativity software

Portuguese Document Review Paralegal. Document Review on eDiscovery platforms such as Relativity. Temporary position as a Portuguese Document Review Paralegal for a top tier law firm in London.