production technology lead in chennai

randstad india
position type
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chennai, tamil nadu
Pharma, healthcare & lifesciences
position type
10 To 18
reference number
randstad india

job description

production technology lead in chennai

Lead molecular IVD (vitro diagnostic device) product development projects through verification and validation
Drive product transfer activities
Manage projects by developing study designs, work streams, timelines and deliverables while driving project execution to meet corporate expectations
Write SOPs and study reports
Conduct test protocols, procedures, and product evaluations
Work within the established design control process for product development and to transfer new products from R&D into manufacturing
Work as a member of a team on product development efforts, as well as on independent development and improvement projects
Works as part of a multi-disciplinary team with other scientists, chemists, engineers and manufacturing personnel on product transfer efforts
Provide data summaries, written reports and oral presentations to R&D, multidisciplinary teams, and to members of the executive team
Demonstrate technical proficiency in molecular techniques
Investigate problem areas and areas of desirable product improvement
Perform high level analysis of experimental results
Provide written reports and oral presentations to executives

To work for a reputed client venturing into molecular diagnostics industry

Client Introduction
A reputed client venturing into molecular diagnostics industry


Scale up, Continuous Improvement, New Technologies
Medical Diagnostics Manufacturing
Leadership, Management, New Site


Engineering. in biology, biochemistry, molecular biology or closely related field with 5+ years of relevant industry experience
Hands-on knowledge of nucleic acid amplification and detection technologies experience
Demonstrated proficiency and expertise in product development through published papers, patents and/or presentations
Demonstrated ability to lead complex projects with minimal supervision
Experience working under design control and with FDA regulatory submissions
Hands-on molecular diagnostic product development experience in a Design Control environment
Isothermal nucleic acid amplification experience a plus