16 English-speaking jobs in Turnhout

Johnson & Johnson seeks an experienced MSAT Sr Principal Engineer Packaging to lead packaging initiatives and programs across secondary and tertiary packaging. This role will own packaging roadmaps, drive innovation, and serve as a subject matter expert for packaging engineering and development.

Johnson & Johnson seeks an experienced MSAT Sr Principal Engineer Packaging to lead packaging initiatives and programs across secondary and tertiary packaging. The role will own packaging roadmaps, drive innovation, and serve as a subject matter expert for packaging engineering and development. This position requires significant experience in pharmaceutical, medical device, or consumer health packaging engineering.

Lead and drive product developments from concept to commercialization, including business continuity, cost-out, and new product development projects. Translate product requirements into specifications, manage project timelines and resources, and communicate progress to cross-functional teams. Act as the R&D project leader, interfacing with customers and suppliers. Develop products following the New Product Design and Development Process and Stage Gate principles. Assist in investigating customer complaints and nonconformances. Develop test methods for new products and assist with product risk management. Conduct literature and patent searches and generate intellectual property disclosures. Provide hands-on technical support to sales, marketing, and manufacturing.

Lead and drive product developments from concept to commercialization, including business continuity, cost-out, and new product development projects. Translate product requirements into specifications, manage project timelines and resources, and communicate progress to cross-functional teams. Act as the R&D project leader, interfacing with customers and suppliers. Develop products following the New Product Design and Development Process and Stage Gate principles. Assist in investigating customer complaints and nonconformances. Develop test methods for new products and assist with product risk management. Leverage internal and external experts to accomplish goals. Conduct literature and patent searches and generate intellectual property disclosures. Provide hands-on technical support to sales, marketing, and manufacturing.

Leads end-to-end recruitment for EMEA & APAC, partnering with hiring managers and HR colleagues to design and execute recruitment strategies. Manages the full recruitment lifecycle, from briefing to onboarding, for a wide range of positions. Drives Talent Acquisition transformation and ensures effective use of recruitment technologies, processes, and metrics. Leads and coordinates the Talent Acquisition community across countries and regions.

Design & Development Engineer will review, assess, and process technical documents for regulatory compliance. The role involves identifying gaps in documentation, coordinating document formatting, and maintaining design history files. Experience in medical device documentation, quality, or regulatory roles is required.

Leads all manufacturing activities, including production planning, capacity management, and resource allocation. Manages the manufacturing team and ensures compliance with FDA 21 CFR Part 820, EU MDR (2017/745), and ISO 13485. Drives continuous improvement initiatives and manages supplier relationships.

Design & Development Engineer will review, assess, and process technical documents for regulatory compliance. The role involves identifying gaps in documentation, coordinating document formatting, and maintaining design history files. Experience in medical device documentation, quality, or regulatory roles is required.

Leads design and development activities for implantable infusion products, ensuring compliance with FDA, EU MDR, and ISO standards. Manages a team of engineers and external partners, overseeing design controls, documentation, and clinical investigations. Collaborates with manufacturing, regulatory, and clinical teams.

Leads all manufacturing activities, including production planning, capacity management, and resource allocation. Manages the manufacturing team and ensures compliance with FDA 21 CFR Part 820, EU MDR (2017/745), and ISO 13485. Drives continuous improvement initiatives and manages supplier relationships.

Leads design and development activities for implantable infusion products, ensuring compliance with FDA, EU MDR, and ISO standards. Manages a team of engineers and external partners, overseeing design controls, documentation, and clinical investigations. Collaborates with manufacturing, regulatory, and clinical teams.

Drive global procurement strategy for core materials and equipment. Optimize Total Cost of Ownership through strategic sourcing and supplier excellence. Lead complex negotiations and manage supplier ecosystems across multiple entities.

Design, develop, and maintain modern applications using Java/Kotlin. Translate business requirements into robust technical solutions and collaborate with Product Owners, Architects, QA Engineers, and fellow Developers.

This internship supports Product Stewardship by synthesizing chemical data from suppliers into client-facing documentation. The intern will review raw material data, map Safety Data Sheets against REACH guidelines, and create Article Information Sheets.

The Commercial Excellence & Digital Specialist acts as the "Digital Engine Room" for the business, bridging the gap between product portfolio and digital infrastructure. Responsibilities include pricing analysis, product management support, market intelligence, dashboard creation, Salesforce management, pricing tool implementation, content coordination, and communications.

Software Engineer (Java/Kotlin) will design, develop, and maintain modern applications using Java/Kotlin. Responsibilities include translating business requirements into technical solutions, collaborating with team members, and integrating software with payment terminals and fueling systems.