Lead coordination and communication for assigned laboratory studies, ensuring clear definition, execution, documentation, and timely completion.
Responsibilities
Serve as primary point of contact for customers regarding assigned studies
Meet with customers to understand testing needs, study requirements, timelines, and expectations
Translate customer requirements into clear direction for laboratory teams
Coordinate study activities from initiation through final reporting
Maintain regular communication with customers regarding study progress, updates, and questions
Requirements
Bachelor’s degree in life sciences or related scientific field
Associate degree or equivalent with relevant laboratory experience
Nice to have: Experience in laboratory testing, life sciences, medical devices, pharmaceuticals, biotechnology, quality, regulated environments, technical customer service, or scientific project coordination
To lead, co-ordinate, supervise and undertake Design and Development projects in the Product Development department of AliveDx (Alba). Record, analyse and reach valid conclusions for complex investigations.
Responsibilities
Assist in planning, organising and undertaking work to Product Development studies and projects with support from the Principal Scientist, Department Leader and the project managers.
Record and analyse the results of experimental work from specific Development projects as assigned by the Principal Scientist and/or Department Leader to meet Design Control requirements in project files and the departmental objectives.
Assist with the supervision and training of other staff within or out with the team to ensure continuous development of staff capabilities.
Monitor the safe operation, control and maintenance of equipment in accordance with established procedures to minimize delays to work programmes and ensure a safe working environment.
Conduct all duties in compliance with local procedures, Good Documentation Practice (GDP) and appropriate regulatory requirements and report any observed breaches to the Department Leader and Technical Compliance Group if applicable.
Production Operator to progress Monoclonal Cell Lines for Cell Banking, Tissue Culture or Fermentation in line with company schedules, SOPs and GMP requirements.
Locations (2)
Edinburgh, Scotland, United Kingdom
Penicuik, Scotland, United Kingdom
Compensation
A starting salary of £26,500 in line with the Real Living Wage.
Responsibilities
Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and relevant regulatory requirements.
Ensure Cultures progress in line with the Manufacturing schedule.
Complete all required documentation and TROPOS transactions accurately, legibly and in a timely manner.
Maintain laboratory stock levels.
Maintain equipment, in accordance with agreed procedures, ensuring equipment is operating correctly.
Requirements
Standard Grade/ National 4/5 or equivalent Mathematics and English
Support the clinical team’s in‑house activities on assigned projects, manage documentation, coordinate trial materials, and assist with monitoring visits.
Responsibilities
Support the clinical team’s in‑house activities on assigned projects
Co‑ordinate and maintain clinical study documentation in the Trial Master Files (TMF)
Support the clinical team in essential document development, collection and management process
Manage the Clinical Trial Management System (CTMS)
Create the Investigator Site Files, co‑ordinating the ordering, dispatch and tracking of trial materials
The Verification Engineer will join the R&D V&V team to test, verify, and validate systems involving hardware, software, and consumables during product development and product care.
Responsibilities
Perform, report and lead test, verification and validation activities for systems which entail hardware, software and consumables.
Define and evaluate system requirements and the corresponding test cases.
Conduct technical investigations, including risk assessments and root-cause analyses.
Ensure compliance with relevant industry standards and regulatory guidelines.
Actively contribute to continuous improvement of processes and practices within V&V.
The Clinical Sample Specialist I is responsible for sample management activities for samples arriving at LabConnect Australia facility, including receiving, storage, processing, and shipment support.
Responsibilities
Sample shipment receipt, inbound tracking documentation and breakdown of kits received
Specimen transport to different areas within the facility
Order requisition registration and accessioning
Specimen labeling
Assist with quality control (QC) of specimens for courier pick-ups, scheduled shipments, ad hoc shipments, specimen destructions and same day shipping packages
Requirements
High school diploma or general education degree (GED)
BA/BS in laboratory science, health science, or business
Associate’s degree
Nice to have: 2 years of clinical research, clinical lab, or relevant experience
Inhouse Clinical Research Associate - SANovotech Global · Australia
Verification EngineerBiotage · Uppsala, Sweden
Clinical Sample SpecialistLabConnect · Port Melbourne, Australia