Associate Scientist-tda

A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

**Your Role**:
As Associate Scientist - Technical Data Analysis (AS -TDA) you will 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.
- 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
- 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

**Who You Are**
- Minimum 2 years of experience in a scientific laboratory role
- 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
- Pursues everything with energy, drive and the need to finish, especially in the face of resistance or setbacks
- Customer oriented and able to relate with clients from different cultures
- Able to maintain effective working relationships with scientists and other lab personnel will be critical for success in the role

**What we offer**: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life