We are excited to be partnering with an innovative and fast-scaling medical device company that is entering a new phase of global operations expansion.
Due to continued growth and increasing global demand, a brand-new and impactful opportunity has arisen for a Senior Director of Operations to lead and evolve the operational functions of a key manufacturing and distribution hub.
Key Responsibilities: Lead the full site operations team, spanning manufacturing, engineering, supply chain, quality, NPI, and support functions. Collaborate with senior leadership to shape and execute long-term strategic operations initiatives. Drive continuous improvement and lean practices across all departments to optimize cost, output, and compliance. Ensure all operational activities meet the highest standards of regulatory compliance within a highly regulated manufacturing environment. Oversee global distribution operations, ensuring products are delivered on time and to the highest quality standards. Manage site budgets, drive financial performance, and ensure resources are aligned to growth plans. Support the industrialization and ramp-up of new products, ensuring readiness for full-scale production.
Ideal Candidate: Extensive experience leading end-to-end manufacturing and operations functions within a regulated environment (medical devices or pharma). A strong preference will be given to candidates with experience in Class III medical devices or similarly complex, high-risk products. Demonstrated success in overseeing both site-level operations and global distribution or supply chain strategies. Strong technical background with the ability to understand and optimize complex manufacturing systems. Proven ability to lead cross-functional teams and manage change in dynamic, high-growth settings. Fluent in both French and English.
If this sounds like something you'd be interested in, I’d love to hear from you directly. Please apply here or feel free to email me at .
Let’s connect!
Join a fast-growing leader in the sports medicine industry! We're looking for a proactive and detail-oriented Clinical Affairs Officer to help drive innovation and ensure the safety and performance of our products. As part of our dynamic R&D team, you'll play a key role in clinical studies, regulatory compliance, and competitive intelligence.
Key Responsibilities: Research & Analysis: Stay on top of clinical and scientific literature, analyzing competitor products for safety, efficacy, and performance. Clinical Safety: Draft and manage Clinical Evaluation Reports (CER), Post-Market Clinical Follow-Up (PMCF) studies, and support post-market surveillance (PMS). Clinical Studies: Write study documentation, implement protocols, monitor product safety in clinical settings, and collaborate with CROs to manage studies effectively. Regulatory Support: Assist in product registration globally and contribute to drafting essential regulatory documents such as CER and Clinical Development Plans (CDP).
Qualifications: Biomedical degree or related field with at least 2 years of experience in clinical and regulatory affairs, ideally in medical devices or diagnostic software. Strong knowledge of medical device regulations (MDD/MDR, ISO 14971, ISO 13485). Proficient in drafting regulatory documents like CER, PMCF, PSUR. Excellent English communication skills (written and editorial). Highly organized, autonomous, and able to work under pressure.
Why Join Us? This is an exciting opportunity to shape the future of sports medicine, working with cutting-edge technologies in a collaborative and dynamic environment. If you're passionate about healthcare innovation and eager to make an impact, we want to hear from you!
An innovative and fast-growing company at the intersection of life sciences and artificial intelligence is seeking a Senior Medical Writer to join their team in France. This position offers the unique opportunity to combine traditional medical writing expertise with cutting-edge AI-enabled solutions that are transforming the way regulatory and clinical documents are produced.
You will work closely with global pharmaceutical clients to implement an AI-powered platform that streamlines the development of regulatory submissions. This is an exciting opportunity to be part of a forward-thinking team redefining clinical content creation while delivering significant value to clients across the drug development lifecycle.
Key Responsibilities: Configure and optimize AI-driven solutions to assist in the creation of regulatory documents. Ensure the accuracy, consistency, and quality of documents in compliance with client and regulatory standards. Review and refine documents produced by internal teams, ensuring they meet industry guidelines and client-specific requirements. Collaborate with cross-functional teams, including Product Managers, Analysts, and Project Managers, to prepare and present platform demos to external stakeholders. Serve as a key point of contact for external subject matter experts during collaborative sessions. Mentor junior team members on best practices for writing and industry standards. Stay informed about the latest trends, regulations, and documentation practices to support both internal development and client engagement.
Key Requirements: Bachelor’s degree in a scientific or technical discipline (advanced degree a plus). 5–7+ years of professional medical writing experience within the pharmaceutical, biotech, or CRO sector. Proven experience authoring Clinical Study Reports (CSRs), Clinical Summaries, or Patient Narratives. Familiarity with regulatory documentation guidelines and medical writing standards. Proficient with MS Office tools and document management systems; strong general tech aptitude. Excellent communication, collaboration, and presentation skills. Ability to manage multiple priorities and deliver to deadlines in a fast-paced environment. Passion for combining life sciences expertise with emerging technologies to deliver value to clients.
I am partnering with an AI Driven fast-moving company using generative AI to design breakthrough materials and chemical processes that help decarbonize heavy industry. By combining cutting-edge machine learning with experimental science, they are building the tools to reinvent how the world makes energy, fertilizer, and more—cleaner, faster, and smarter.
After a significant round of funding, they are looking to expand the team with senior hires in different areas of the business.
Lead Data Engineer
Responsibilities
Lead and execute the internal data strategy across the organization, aligning with AI and scientific objectives. Design and manage data pipelines for ingestion, processing, and transformation of diverse datasets (LLMs, physical-chemical, experimental, graph data, etc.). Lead the deployment of machine learning models in a scalable, secure cloud environment (e.g., AWS, GCP, or Azure). Structure and maintain internal databases/platforms to optimize for performance and usability by AI systems, researchers, and engineers. Develop robust tools for querying and accessing data, enabling self-service and automation across teams. Collaborate closely with a multidisciplinary team of scientists, machine learning experts, and software engineers to accelerate R&D. Architect how data is hosted, versioned, and accessed, ensuring integrity, scalability, and reproducibility. Take full ownership of your projects—from design to implementation to ongoing maintenance and improvements.
Requirements
5+ years of industry experience in data engineering, ML infrastructure, or DevOps roles. Proven DevOps / infrastructure experience, including CI/CD, containerization (Docker, Kubernetes), and automation workflows. Experience with at least two major cloud providers (e.g., AWS, GCP, Azure). Strong familiarity with multi-modal data, including graph structures, natural language, lab/experimental data, and imaging formats. A research mindset with the ability to translate emerging academic and open-source developments into production-ready systems. Deep curiosity and ability to stay current with advances in machine learning, data infrastructure, and scientific computing. A genuine interest in environmental and sustainability challenges, and a desire to work on meaningful solutions with real-world impact. Strong programming skills (e.g., Python, Bash) and experience with modern data and ML tooling (e.g., Airflow, DVC, MLflow, Spark).
Following your application Jay Robins, a specialist AI Recruitment consultant will discuss the opportunity with you in detail. He will be more than happy to answer any questions relating to the industry and the potential for your career growth. The conversation can also progress further to discussing other opportunities, which are also available right now or will be imminently becoming available. This position has been highly popular, and it is likely that it will close prematurely. We recommend applying as soon as possible to avoid disappointment.
Please click ‘apply’ or contact Jay Robins for any further information. Email:
An innovative and fast-growing company at the intersection of life sciences and artificial intelligence is seeking a Senior Medical Writer to join their team in France. This position offers the unique opportunity to combine traditional medical writing expertise with cutting-edge AI-enabled solutions that are transforming the way regulatory and clinical documents are produced. You will work closely with global pharmaceutical clients to implement an AI-powered platform that streamlines the development of regulatory submissions. This is an exciting opportunity to be part of a forward-thinking team redefining clinical content creation while delivering significant value to clients across the drug development lifecycle. Key Responsibilities: Configure and optimize AI-driven solutions to assist in the creation of regulatory documents. Ensure the accuracy, consistency, and quality of documents in compliance with client and regulatory standards. Review and refine documents produced by internal teams, ensuring they meet industry guidelines and client-specific requirements. Collaborate with cross-functional teams, including Product Managers, Analysts, and Project Managers, to prepare and present platform demos to external stakeholders. Serve as a key point of contact for external subject matter experts during collaborative sessions. Mentor junior team members on best practices for writing and industry standards. Stay informed about the latest trends, regulations, and documentation practices to support both internal development and client engagement. Key Requirements: Bachelor’s degree in a scientific or technical discipline (advanced degree a plus). 5–7+ years of professional medical writing experience within the pharmaceutical, biotech, or CRO sector. Proven experience authoring Clinical Study Reports (CSRs), Clinical Summaries, or Patient Narratives. Familiarity with regulatory documentation guidelines and medical writing standards. Proficient with MS Office tools and document management systems; strong general tech aptitude. Excellent communication, collaboration, and presentation skills. Ability to manage multiple priorities and deliver to deadlines in a fast-paced environment. Passion for combining life sciences expertise with emerging technologies to deliver value to clients.
Join a fast-growing leader in the sports medicine industry! We're looking for a proactive and detail-oriented Clinical Affairs Officer to help drive innovation and ensure the safety and performance of our products. As part of our dynamic R&D team, you'll play a key role in clinical studies, regulatory compliance, and competitive intelligence. Key Responsibilities: Research & Analysis: Stay on top of clinical and scientific literature, analyzing competitor products for safety, efficacy, and performance. Clinical Safety: Draft and manage Clinical Evaluation Reports (CER), Post-Market Clinical Follow-Up (PMCF) studies, and support post-market surveillance (PMS). Clinical Studies: Write study documentation, implement protocols, monitor product safety in clinical settings, and collaborate with CROs to manage studies effectively. Regulatory Support: Assist in product registration globally and contribute to drafting essential regulatory documents such as CER and Clinical Development Plans (CDP). Qualifications: Biomedical degree or related field with at least 2 years of experience in clinical and regulatory affairs, ideally in medical devices or diagnostic software. Strong knowledge of medical device regulations (MDD/MDR, ISO 14971, ISO 13485). Proficient in drafting regulatory documents like CER, PMCF, PSUR. Excellent English communication skills (written and editorial). Highly organized, autonomous, and able to work under pressure. Why Join Us? This is an exciting opportunity to shape the future of sports medicine, working with cutting-edge technologies in a collaborative and dynamic environment. If you're passionate about healthcare innovation and eager to make an impact, we want to hear from you!
I am partnering with an AI Driven fast-moving company using generative AI to design breakthrough materials and chemical processes that help decarbonize heavy industry. By combining cutting-edge machine learning with experimental science, they are building the tools to reinvent how the world makes energy, fertilizer, and more—cleaner, faster, and smarter. After a significant round of funding, they are looking to expand the team with senior hires in different areas of the business. Lead Data Engineer Responsibilities Lead and execute the internal data strategy across the organization, aligning with AI and scientific objectives. Design and manage data pipelines for ingestion, processing, and transformation of diverse datasets (LLMs, physical-chemical, experimental, graph data, etc.). Lead the deployment of machine learning models in a scalable, secure cloud environment (e.g., AWS, GCP, or Azure). Structure and maintain internal databases/platforms to optimize for performance and usability by AI systems, researchers, and engineers. Develop robust tools for querying and accessing data, enabling self-service and automation across teams. Collaborate closely with a multidisciplinary team of scientists, machine learning experts, and software engineers to accelerate R&D. Architect how data is hosted, versioned, and accessed, ensuring integrity, scalability, and reproducibility. Take full ownership of your projects—from design to implementation to ongoing maintenance and improvements. Requirements 5+ years of industry experience in data engineering, ML infrastructure, or DevOps roles. Proven DevOps / infrastructure experience, including CI/CD, containerization (Docker, Kubernetes), and automation workflows. Experience with at least two major cloud providers (e.g., AWS, GCP, Azure). Strong familiarity with multi-modal data, including graph structures, natural language, lab/experimental data, and imaging formats. A research mindset with the ability to translate emerging academic and open-source developments into production-ready systems. Deep curiosity and ability to stay current with advances in machine learning, data infrastructure, and scientific computing. A genuine interest in environmental and sustainability challenges, and a desire to work on meaningful solutions with real-world impact. Strong programming skills (e.g., Python, Bash) and experience with modern data and ML tooling (e.g., Airflow, DVC, MLflow, Spark). Following your application Jay Robins, a specialist AI Recruitment consultant will discuss the opportunity with you in detail. He will be more than happy to answer any questions relating to the industry and the potential for your career growth. The conversation can also progress further to discussing other opportunities, which are also available right now or will be imminently becoming available. This position has been highly popular, and it is likely that it will close prematurely. We recommend applying as soon as possible to avoid disappointment. Please click ‘apply’ or contact Jay Robins for any further information. Email:
We are excited to be partnering with an innovative and fast-scaling medical device company that is entering a new phase of global operations expansion. Due to continued growth and increasing global demand, a brand-new and impactful opportunity has arisen for a Senior Director of Operations to lead and evolve the operational functions of a key manufacturing and distribution hub. Key Responsibilities: Lead the full site operations team, spanning manufacturing, engineering, supply chain, quality, NPI, and support functions. Collaborate with senior leadership to shape and execute long-term strategic operations initiatives. Drive continuous improvement and lean practices across all departments to optimize cost, output, and compliance. Ensure all operational activities meet the highest standards of regulatory compliance within a highly regulated manufacturing environment. Oversee global distribution operations, ensuring products are delivered on time and to the highest quality standards. Manage site budgets, drive financial performance, and ensure resources are aligned to growth plans. Support the industrialization and ramp-up of new products, ensuring readiness for full-scale production. Ideal Candidate: Extensive experience leading end-to-end manufacturing and operations functions within a regulated environment (medical devices or pharma). A strong preference will be given to candidates with experience in Class III medical devices or similarly complex, high-risk products. Demonstrated success in overseeing both site-level operations and global distribution or supply chain strategies. Strong technical background with the ability to understand and optimize complex manufacturing systems. Proven ability to lead cross-functional teams and manage change in dynamic, high-growth settings. Fluent in both French and English. If this sounds like something you'd be interested in, I’d love to hear from you directly. Please apply here or feel free to email me at . Let’s connect!
An innovative and fast-growing company at the intersection of life sciences and artificial intelligence is seeking a Senior Medical Writer to join their team in France. This position offers the unique opportunity to combine traditional medical writing expertise with cutting-edge AI-enabled solutions that are transforming the way regulatory and clinical documents are produced.
You will work closely with global pharmaceutical clients to implement an AI-powered platform that streamlines the development of regulatory submissions. This is an exciting opportunity to be part of a forward-thinking team redefining clinical content creation while delivering significant value to clients across the drug development lifecycle.
Key Responsibilities:
Configure and optimize AI-driven solutions to assist in the creation of regulatory documents.
Ensure the accuracy, consistency, and quality of documents in compliance with client and regulatory standards.
Review and refine documents produced by internal teams, ensuring they meet industry guidelines and client-specific requirements.
Collaborate with cross-functional teams, including Product Managers, Analysts, and Project Managers, to prepare and present platform demos to external stakeholders.
Serve as a key point of contact for external subject matter experts during collaborative sessions.
Mentor junior team members on best practices for writing and industry standards.
Stay informed about the latest trends, regulations, and documentation practices to support both internal development and client engagement.
Key Requirements:
~ Bachelor’s degree in a scientific or technical discipline (advanced degree a plus).
~5–7+ years of professional medical writing experience within the pharmaceutical, biotech, or CRO sector.
~ Proven experience authoring Clinical Study Reports (CSRs), Clinical Summaries, or Patient Narratives.
~ Familiarity with regulatory documentation guidelines and medical writing standards.
~ Proficient with MS Office tools and document management systems; strong general tech aptitude.
~ Excellent communication, collaboration, and presentation skills.
~ Ability to manage multiple priorities and deliver to deadlines in a fast-paced environment.
~ Passion for combining life sciences expertise with emerging technologies to deliver value to clients.
Join a fast-growing leader in the sports medicine industry! Biomedical degree or related field with at least 2 years of experience in clinical and regulatory affairs, ideally in medical devices or diagnostic software.
Strong knowledge of medical device regulations (MDD/MDR, ISO 14971, ISO 13485).
Excellent English communication skills (written and editorial).
