Process Scientist L - Singapore - Merck KGaA Darmstadt Germany

Merck KGaA Darmstadt Germany

Verified Company

Singapore

1 week ago

Posted by:

Wei Jie

beBee Recruiter

Description

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.

We are a leading science and technology company.

Our life science business offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses.

Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.

As Process Scientist - Viral Clearance, you will deliver Viral Clearance validation studies for biopharmaceutical companies across the APAC region.

Within the our Company's Life Science Services team, you will have scientific expertise in Viral Clearance with in-depth understanding of biopharma downstream processing (chromatography, virus filtration and low pH/chemical inactivation) and virology.

You will ensure projects are carried out with the appropriate scientific and regulatory compliance oversight and you will provide technical expertise during client meetings, lead technology transfer of client processes, oversee the generation of batch records, coordinate execution of scale-down process in the lab and lead technical trouble shooting and investigations.

You will also have the technical expertise to advice and support GLP / GMP operations and audits, and you will maintain an in-depth understanding of BioReliance services and technical principles as well as advances in the field.

The ability to maintain effective working relationships with clients (external) and development services, project management, quality, sales and laboratory personnel (internal) will be critical for success in the role.

Your Role:

Acts as Process Scientist for viral clearance studies and holds responsibility for process aspects of client studies, including collection of client process information, generation of process records and Akta methods, client communication of results, resolving process issues and ensuring on time delivery of provide clearance studies
Works within the viral clearance laboratory providing handson support, training and guidance to laboratorybased personnel in the areas of process science, chromatography, virus filtrations and labscale downstream models
Effectively collaborates with study management, testing lab functions, quality and PMO to ensure routine and complex client studies are completed on time, to the appropriate scientific and regulatory standards
Plans to successfully transfer client processes into the BioReliance laboratories according to the client's technical documentation and SOP's
Prepares high quality client process specific protocols and methods for the performance of chromatography, inactivation and filtration steps
Responds to audit observations through the BioReliance Integrated Quality System (Trackwise)
Raises and progresses deviation and Corrective or Preventative Action (CAPA) records in a timely manner
Leads complex projects related to area of operational expertise
Leads the set up of new process technology to be performed in Client Labs.
Leads process improvements within the laboratory to improve quality and performance
Acts as process science and technical consultant to support departmental investigations, client process queries, supplier audits and client/regulatory inspections
Ensures a safe and healthy work environment at all times by not only complying with but actively embracing health and safety policies and procedures to ensure the welfare and safety of self and others within the workplace

WHO YOU ARE:

Minimum 4 to 6 years of experience in a scientific laboratory role (preferably with 23 years of experience in leading scientific project)
Minimum 2 to 3 years of experience in a regulated environment (GLP/GMP) preferred
Demonstrate scientific understanding in downstream bioprocessing (filtration and chromatography)
Handson experience with liquid chromatography systems (e.g. Akta Pure/Avant systems), with demonstrated ability to program run methods, and able to perform effective troubleshooting in lab procedures
Able to customize scaledown system setup for nonroutine client processes is a bonus
Experience in setting up laboratory is a bonus
Quality mindset and advanced understanding of Good Manufacturing/Laboratory Practices
Prior experience in any of the following areas will be desirable:
Prior experience in a regulated environment (GLP/GMP)
Prior experience in Proce