SEC Group · 6 hours ago
Research And Development Engineer
SEC Group is seeking a Senior Research and Development Engineer to lead the research, design, and development of components for critical bioprocessing applications. This role involves supporting innovation and product development through all stages, ensuring compliance with regulatory standards, and driving continuous improvement in product performance.
Responsibilities
Translate business needs and market trends into product requirements and innovative engineering solutions
Stay current with emerging technologies, materials, and industry trends to maintain competitive advantage
Drive innovation by exploring new technologies, tools, and methodologies
Support intellectual property strategies by identifying patentable technologies, working with legal team
Partner with cross-functional teams to ensure successful product development and launch, adhering to established stage-gated process and governance model
Effectively project manage timelines, budgets, and resources to deliver high-quality results
Oversee the planning, design, development, prototyping, testing, and validation of new products and technologies
Conduct risk assessments using FMEA framework, and drive risk mitigations as required. Lead design and drawing reviews as needed
Ensure compliance with applicable regulatory, safety, and quality standards throughout the development process
Lead problem-solving, corrective, and preventative actions around product concerns originating both external and internal to the organization
Analyse data from validation tests to determine whether systems and processes meet required criteria and specifications
Maintain technical records within design history files
Drive continuous improvement in product performance, design for manufacturability (DFM), and design for cost-effectiveness (DTC)
Develop and implement engineering best practices, design standards, and documentation protocols. Author SOP’s, Work Instructions and Templates
Support Product Delivery Teams (PDT), including creating and or reviewing quality documents, participating in Corrective And Preventive Action (CAPA) implementation, and generating or supporting ECR (Engineering Change Request) & ECO (Engineering Change Order) activities
Work with Scientists and Engineers internally and externally to assess and develop appropriate design and manufacturing specifications
Perform other duties as assigned
Qualification
Required
Bachelor's degree in Mechanical, Electrical, Biomedical, or related Engineering field
7+ years of engineering experience within a biotechnology or pharmaceutical manufacturing facility
4+ years of Single-Use Technology (SUT) design experience
Demonstrated expertise in the design of molded plastic parts and assemblies for fluid handling of leak-proof applications
Thorough understanding of industry standards and regulatory guidelines
Proven track record in product development, from concept through commercialization
Ability to manage multiple projects in a fast-paced, collaborative environment
Results-driven mindset with keen sense of urgency and ability to deliver ahead of deadlines
Demonstrated attention to detail
Excellent follow-up skills
Must be self-motivated, amendable to a variety of work projects and work efficiently independently and as part of a team
Strong knowledge of design controls, prototyping technologies such as 3D printing, testing, and validation methodologies
Able to read and comprehend and interpret documents such as drawings, BOM's, blueprints, and operating procedures
Maintain organized and controlled records of all drawings and BOM's
Solid understanding of mathematical fundamentals of plane and solid geometry, fractions, percentages, ratios, and proportions applied to practical situations
Ability to interpret complex data sets, identify patterns, and draw meaningful conclusions
Expert knowledge and demonstrated hands-on experience with CAD software, both 3D and 2D
Proficient with Microsoft Office Suite or related software
Excellent verbal and written communication skills
Strong interpersonal skills: ability to interact with staff at all levels within the organization
Proactive approach to identifying opportunities for improvement and driving positive change
Develop and maintain positive rapport and working relationships with other personnel across the organization in support of initiatives to execute product improvements and enhancements
Experience working in a GMP (Good Manufacturing Practice) or laboratory environment
Preferred
Master's degree
Preferred experience includes design with tubing, bags, and filling needles
Knowledge of ISO 13485, ASME BPE, or related design standards