AR-GE Sorumlusu

BOME TRIVITRON SANAYİ ÜRÜNLERİ DIŞ TİC AŞ

General Purpose

We are looking for a full-time R&D Specialist to join our Research and 

Development team based in Ostim, Ankara and work on designing 

In Vitro Diagnostic (IVD) products.

 
 
Main Job Tasks and Responsibilities

• Design and perform experiments in compliance with GLP.
• Work with broad range of chemicals and human blood products under 

            regulated and controlled conditions.

• Perform routine instrument maintenance.
• Keep prompt, accurate and precise records; prepare and revise traceable 

            technical documentation in compliance with quality assurance tasks in 

            R&D Lab.

• Analyze the data using appropriate methodology and tools; prepare 

           summaries and report to the R&D Manager.

• Ensure assay development processes meet the project mini dead-lines, 

            milestones and timelines.

• Adherence to CLSI guidelines where applicable; and to requirements 

           outlined in ISO 13485.

• Perform minor and major risk assessment activities in every relevant 

           aspect of laboratory performance and project design.

• Prepare and perform intra-departmental training upon 

           requirement.

• Prepare SOPs and perform inter-departmental training to facilitate 

           and complete design transfer to manufacturing.

• Attendance and participation in R&D meetings and report of progress

           to the R&D Manager.

• Prepare and present written and oral reports to internal and external 

           audiences as required.
Education and Experience

• Bachelor degree in biological sciences or chemistry 

           (preference will be given to candidates with Master’s or PhD in a 

           relevant topic)

• Minimum 2 years hands-on lab experience (PhD will be preferred)
• Competency in immunoassay techniques
• Competency in protein and DNA analysis techniques
• Knowledge of raw materials
• Knowledge of laboratory safety standards and compliance
• Knowledge of quality systems and standards (such as ISO 13485, CLSI) 

            will be preferred

• Knowledge of clinical chemistry and related analysis techniques 

            will be preferred
 
Key Competencies

• good laboratory practice
• innovative and analytical thinking
• strong problem solving skills
• planning and organizing
• self-discipline and responsibility
• time management
• attention to detail
• decision-making
• interpersonal and communication skills
• team work
• fluency in written and spoken English
• solid computer skills
• stress tolerance