Jobs at Smithers - Medical Device Testing

Perform ligand-binding assays (ELISA/MSD) and bioanalytical method development, validation, and sample analysis under GLP/GCP/CLIA. Interpret and summarize data, maintain records, review colleagues' data, follow SOPs, and support lab operations safely.

The Business Development Manager will expand client relationships in Europe, targeting medical device and pharmaceutical sectors, and developing strategic account plans, while also supporting marketing and attending industry events.

The Senior Conference Producer will lead B2B conference production, develop agendas, secure speakers, and manage event execution, contributing to strategic growth plans.

Plan, coordinate, and execute marketing initiatives for Information Security Services including website and social content, email campaigns, SEO, lead generation, event/trade show support, CRM management, and campaign analytics to drive brand awareness and sales.

Generate new business opportunities for Information Security Services through outbound prospecting (calls, email, social), qualify leads, schedule meetings, track activity in CRM, and meet lead-generation KPIs while collaborating with Sales and Marketing.

Lead and deliver analytical method development and validation (LC-MS/MS, GC) for environmental matrices under GLP and non-GLP. Manage a small technical team, act as Study Director/contributing scientist, engage with clients, interpret complex data, produce regulatory-ready reports, support audits/inspections, and drive continuous improvement and emerging contaminant strategies.

Manage end-to-end medical device testing projects: prepare quotes, control scope changes, host client programme calls, liaise with technical and commercial stakeholders, support cross‑functional labs, improve systems, and represent the company at industry events.

Conduct physical testing of medical devices, manage projects, prepare reports, support validation, perform statistical analysis, and ensure compliance with quality standards.

Design, develop, and assess bioanalytical assays (PK, ADA, Nab); support method validation, troubleshoot assays, draft SOPs, and provide technical guidance. Maintain GLP/GCP/CLIA compliance, follow safety and SOPs, and use Watson LIMS and statistical tools to analyze and report bioanalytical data.

Perform QC review of data tables, reports, run folders and notebooks; create/verify data summary tables from Watson LIMS and Excel; organize and archive study materials; identify and document deviations; assist Project Manager with timelines, drafting analytical plans/reports (Study Coordinator II), attend client calls, and ensure timely responses to QC/QA findings in a GLP/GCP laboratory environment.

Lead and execute polymer materials test programmes, liaise with clients, design and build test rigs, develop new test methods, produce quality data and technical reports, and support equipment maintenance and organisation.

Perform complex analytical testing of cannabis and derived products using HPLC/LCMS, GC-MS, ICP-MS and microbial platforms. Maintain chain-of-custody, follow SOPs and ISO/IEC 17025, run calibrations and maintenance, analyze data and prepare reports, support QC/QA, assist method validation and train junior staff.

As a Marketing Operations & Data Research Apprentice, you will conduct data research, support CRM operations, enhance data quality, and assist marketing efforts.

Manage complex medical device testing projects from proposal to delivery, collaborating with cross-functional teams and ensuring operational excellence.

The Project Manager will develop and lead testing programs, build client relationships, and provide technical support and leadership in the materials testing business.

Conduct ISO audits (quality, environmental, OHS), develop and execute audit plans, assess facilities and documentation, identify non-conformities and improvement opportunities, maintain records and auditor credentials, submit audit documentation and expense reports, and support clients through certification using BOS audit management platform.

Perform third-party management system assessments and certification activities across quality, environmental, OHS, automotive, aerospace, medical device, and information security standards. Verify conformance to standards and accreditation requirements, prepare audit reports, maintain impartiality, and build client relationships while ensuring certification schemes meet industry and internal procedures.

Perform IATF 16949 and ISO 9001:2015 audits for automotive clients, develop and execute audit plans, evaluate documentation and processes, identify nonconformities, maintain records and auditor credentials, and deliver audit reports and client support.