Associate Scientist - Technical Data Analysis

Work Your Magic with us!  

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

Your Role:

As Associate Scientist – Technical Data Analysis (AS –TDA) you will be part of the Process Solutions Services team that designs and delivers Viral Clearance validation studies for biopharmaceutical companies across the APAC region. The AS - TDA is responsible for the preparation of Final Reports and Certificates of Analysis using data obtained from GLP/GMP assays performed across all Bioreliance Biotesting Lab in Singapore.  In collaboration with the laboratory personnel, the AS - TDA summarizes the life cycle, technical processes and assay results of a sample in a Final Report. The AS - TDA will work closely with the Study Directors to prepare the study file and generate the final report on time. The AS - TDA will review batch records, process data and perform trend analysis data to ensure consistent assay performance and scientific integrity of the study.

The post holder need to have an understanding of technical/ scientific observations and ensure all documentation generated fulfills quality and regulatory standards and practices (GLP or GMP) as well as client specific requirements when reporting assays. The post holder will be proficient in generating reports in English and is able to translate to Mandarin when required.

The post holder will be able to perform the following functions.

What You Do:

• Summarizes technical data into a high quality report or certificate of analysis as required, in a timely manner
• Works closely with study management to prepare study files and perform technical data review of executed lab records
• Is familiar with study-specific protocols, technical specifications, applicable SOPs and regulatory requirements
• Prepares study reports and any applicable study associated Final Report/Certificate of Analysis amendments according to specific client requests to achieve on time delivery.  Addresses comments on these study reports following Study Director review and Quality Assurance audit
• Generates, controls and tracks revisions to all appropriate Report/Certificate templates
• Translates reports written in English to Mandarin when required
• Leads investigations and implements CAPAs and change controls ensuring records are closed in accordance with the assigned timelines
• Owns projects to enable continuous improvement and drive a quality culture
• Ensures a safe and healthy work environment at all times by not only complying with but actively embracing health and safety policies and procedures, ensuring the safety of yourself and others within the workplace
• Review Right First Time (RFT) metrics with the appropriate personnel in order to drive down error rates.
• Input dates into Information management systems and prepare study files for archiving
• Reviews laboratory records and performs statistical analysis to calculate virus titers log reduction factors
• Provides hands-on support to the lab team by performing virus titration assays, virus infectivity reads and virus titre calculations when required
• Performs trend analysis to ensure the assay remains in the qualified state of control
• Prepares system reports in support of huddles and metrics tracking

 
The above list of job duties is not exclusive or exhaustive and the post holder will be required to undertake such tasks as may reasonably be expected within the scope of the post.

Who You Are

• Bachelor degree in Biological Sciences or higher degree in relevant scientific subject
• Minimum 2 years of experience in a scientific laboratory role with previous experience in scientific writing
• Previous experience working in a regulated environment (GLP/GMP) would be advantageous
• Computer literacy and entry of data into databases (LIMS, ELN, SAP, etc.)
• Ability to complete documentation (both handwritten and electronic) neatly and accurately
• Adheres to health and safety procedures and actively takes necessary action when encountering unsafe situations
• Adheres to SOPs and protocols, and ensures compliance to site policies and regulations
• Is seen as a team player, cooperative and encourages collaboration
• Is customer oriented and able to relate with clients from different cultures
• Is able to maintain effective working relationships with scientists and other lab personnel will be critical for success in the role 
• Ability to work overtime or flexible shifts from time to time to cover testing requirements 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!