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Product development
Concept development, requirements, architecture, design verification and transfer preparation for medical products.
ENGINEERING FOR PHARMA & MEDICAL TECHNOLOGY
From product idea to industrially viable medical technology.
SUR MEDTECH develops products, assemblies and enabling technologies for pharmaceutical and medical applications. Swiss engineering competence is combined with Türkiye's industrial and health-technology ecosystem to create a clear path to qualification and industrial implementation.
SUR MEDTECHSwiss engineering competence · Türkiye industrial ecosystem
CORE COMPETENCIES
Engineering across the complete development system.
Our engineering approach is shaped by Swiss precision, structured development and quality discipline. We work where product, component, material, process and industrial requirements must function together.
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Assembly development
Functional assemblies, interfaces, tolerance concepts, component integration and design-for-assembly.
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Technology development
Material, process, tooling and automation concepts developed around the required product performance.
04
Industrialization engineering
A structured path from prototypes and samples to qualified processes and scalable production.
AUTOMATION & VALIDATION
High-precision production systems for quality-critical products.
We engineer highly automated production lines from material characterization and process development through to the industrialized product. Sensitive camera inspection, controlled process data and GMP-oriented qualification and validation are designed into the manufacturing concept from the outset.
These capabilities support both our proprietary product platforms and external customer projects as independent engineering services.
QUALITY & COMPLIANCE FRAMEWORK
Designed for regulated development and GMP-oriented industrialization.
Applicable standards and regulatory expectations are translated into requirements, risks, design controls, process evidence and qualification plans for each project.
QUALITY BY DESIGNRequirements · Risk · Evidence · Control
Good Manufacturing Practice
Controlled processes, documentation, qualification and traceability
Medical device quality management
Risk-based product development and controlled design records
Medical device risk management
Hazard analysis, risk controls and benefit-risk evidence
Primary pharmaceutical packaging
GMP principles for materials and packaging components
Cleanroom environments
Cleanliness concepts, monitoring and controlled production zones
Standards are applied according to product, process and customer scope. References describe our engineering framework and do not constitute a certification claim.
SECTOR FOCUS
Specialized for regulated, quality-critical applications.
Pharmaceutical systems
Primary packaging, drug-delivery interfaces and technical solutions for sensitive pharmaceutical programs.
Medical devices
Product and component engineering with traceable requirements, risk thinking and verification planning.
Production technologies
Tooling, injection molding, assembly, inspection and qualification concepts for controlled manufacturing.
HOW WE WORK
Evidence-driven development from requirement to transfer.
01Define requirements
02Develop product and assemblies
03Validate technology
04Qualify the process
05Transfer to production
ORGANIZATION
An integrated team built around development and industrial execution.
Our organization connects commercial responsibility, financial control, technical leadership and quality oversight with the specialist disciplines required to bring regulated products into production.
Executive leadership
COO
Operations, programs and industrial execution
CFO
Finance, investment control and governance
CTO / Engineering Lead
Technology strategy and technical accountability
Engineering & operational functions
Sales & Business Development
Domestic and international markets, customer development and strategic partnerships
Mechanical Engineering
Product, component and assembly engineering
Design Engineering
CAD, drawings, tolerances and design documentation
Automation & IT Engineering
Controls, data systems, software and integration
Quality & Validation
GMP, qualification, validation and traceability
Industrial Engineering
Processes, tooling, capacity and production transfer
PROPRIETARY PLATFORM
SURject® demonstrates our integrated development capability.
Our COC prefilled-syringe platform brings together material science, product architecture, component development and industrialization planning in one controlled technology program.
Discover SURject®
CAREERS
Build regulated medical technology with us.
We are building an interdisciplinary team for product development, automation and industrialization. We welcome applications from specialists who combine technical depth with disciplined execution.
Please send a concise profile, your area of expertise and relevant project experience.info@rnd-teh.com
Current areas of interest
Domestic Sales Manager
Develop Türkiye-based customers for technical plastic components, medical products and engineering services.
Key responsibilities
- Build and manage a qualified B2B sales pipeline
- Translate customer needs into structured technical opportunities
- Coordinate quotations, samples and commercial follow-up
Your profile
Apply for this role- Experience in technical sales, preferably plastics, injection molding, medical or pharma
- Understanding of drawings, materials and manufacturing processes
- Professional Turkish and working English
International Sales & Business Development Manager
Develop export markets, strategic accounts and international technology partnerships.
Key responsibilities
- Identify and qualify international customers and partners
- Lead technical-commercial discussions from first contact to program award
- Represent SUR MEDTECH at relevant industry events and customer meetings
Your profile
Apply for this role- International B2B sales experience in technical plastics, medtech, pharma or contract manufacturing
- Strong commercial communication and negotiation skills
- Professional English; German or another export-market language is an advantage
Mechanical Engineer
Develop regulated products, components and functional assemblies from concept to industrial transfer.
Key responsibilities
- Create product concepts, calculations and tolerance strategies
- Support material selection, prototyping and design verification
- Work with tooling, automation and quality teams
Your profile
Apply for this role- Degree in mechanical, plastics or product engineering
- Experience with polymer components and injection-molded parts
- Knowledge of DFM, risk-based development and technical documentation
Design Engineer / CAD Designer
Convert product architecture into production-ready 3D models, drawings and controlled design documentation.
Key responsibilities
- Develop detailed CAD models and assemblies
- Create drawings, GD&T and tolerance chains
- Maintain controlled design revisions and release packages
Your profile
Apply for this role- Advanced 3D CAD experience
- Strong knowledge of plastic-part and mold-compatible design
- Accurate, structured work with technical drawings and BOMs
Automation Engineer
Engineer high-precision assembly and inspection systems for quality-critical production.
Key responsibilities
- Develop automation, handling and machine concepts
- Integrate sensors, camera inspection and process controls
- Support commissioning, qualification and performance testing
Your profile
Apply for this role- Experience in PLC, motion, robotics or machine vision
- Understanding of automated assembly for plastic or medical components
- Structured troubleshooting and commissioning capability
IT & Systems Engineer
Connect production equipment, quality data and secure digital workflows.
Key responsibilities
- Design system interfaces and production-data flows
- Support traceability, access control and operational IT
- Integrate equipment, databases and reporting solutions
Your profile
Apply for this role- Experience with industrial IT, system integration or software engineering
- Knowledge of databases, APIs and secure infrastructure
- Interest in validated and traceable manufacturing environments
Quality & Validation Engineer
Build evidence that products, processes and automated systems perform as intended.
Key responsibilities
- Plan qualification and validation activities
- Develop protocols, risk assessments and traceability records
- Coordinate deviations, CAPA and controlled documentation
Your profile
Apply for this role- Experience with GMP, ISO 13485 or regulated manufacturing
- Knowledge of IQ/OQ/PQ and risk-management methods
- Precise documentation and cross-functional communication skills
INNOVATION ECOSYSTEM
Developed within Türkiye's industrial and health-technology landscape.
Institutional support
Supported within Türkiye's industrial and health innovation ecosystem.
The institutions shown below form part of Türkiye's relevant industrial, health-technology and SME support landscape. Any project-specific relationship is evidenced only by the applicable official program or project documentation.
Logo display identifies the relevant institutional ecosystem. It does not by itself represent funding approval, endorsement, regulatory authorization, an investment guarantee or a commitment to future financing. Only official decisions and program documentation define the scope and current status of any support.
WORK WITH SUR MEDTECH
Choose the right entry point for your project.
Development & Industry Partners
Evaluate products, technical work packages, samples and future supply programs in the Partner Portal.
Open Partner PortalQualified Investors
Review the technology platform, industrial program, financial case and controlled evidence in the Investor Portal.
Open Investor Portal