Job Description

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 Process Scientist - Viral Clearance, you will deliver Viral Clearance validation studies for biopharmaceutical companies across the APAC region. Within theProcess Solutions 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 ofBioReliance 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.

Brief role description:

• 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 complete clearance studies
• Works within the viral clearance laboratory providing hands-on support, training and guidance to laboratory based personnel in the areas of process science, chromatography, virus filtrations and lab-scale 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
• Leads by example, acts as subject matter expert, offers scientific coaching and mentoring to other staff members
• 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

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:
Education:

• Master degree in Chemical Engineering, Biological Sciences or higher degree in related scientific subject

Experience:

• Minimum 4 to 6 years of experience in a scientific laboratory role (preferably with 2-3 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)
• Hands-on experience with Akta Pure/Avant systems, with demonstrated ability to program AKTA methods, and able to perform effective trouble-shooting in lab procedures
• Able to customize scale-down system set-up for non-routine 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 MSAT or Process Development (protein purification) in a biopharmaceutical company or related industry
  • Experience of working in Biosafety Level 2 laboratory
  • Experience of BLA, IND dossier preparation is a plus

Knowledge & Skills:

• Computer literacy and entry of data into databases (LIMS, ELN, SAP, etc.)
• Ability to complete documentation (both handwritten and electronic) neatly and accurately
• Train the trainer

Core competencies:

• Organization skills
  • Demonstrates customer centricity
  • Through effective communication, provides the information people need to know to do their jobs
  • Has strong organizational skills with the ability to use available resources effectively
• Problem solving and drive
  • Can learn new skills and acquire knowledge rapidly
  • Uses logic to solve complex problems and can troubleshoot effectively
  • Is self-motivated and action-orientated, determined to provide best-in-class service and seizes more opportunities than others
  • Pursues everything with energy, drive and the need to finish, especially in the face of resistance or setbacks
  • Can be counted on to achieve goals, constantly and consistently, pushes self and others for results
• Professional and technical skills
  • Has the functional and technical knowledge and skills to do the job at a high level of accomplishment
  • Shows sound judgment in decision making
  • Comes up with new and unique ideas and adds value in brainstorming settings
  • Deals effectively with pressure; remains optimistic and persistent, even under adversity
  • Puts safety first by adhering to health and safety procedures and actively takes necessary action when encountering unsafe situations
• Personal and interpersonal skills
  • Relates well to all kinds of people in the organization, builds constructive and effective relationships using diplomacy and tact
  • Is seen as a team player, cooperative and encourages collaboration
  • Communicates effectively with others and handles conflict effectively
  • The ability to maintain effective working relationships with lab personnel, global and internal stakeholders will be critical for success in the role

ADDITIONAL LOCAL NEEDS

• 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 celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!

Curious? Chat with one of our curious minds on our interactive Q&A platform and catch a glimpse of our people, values, and culture. You can also apply and find more information at https://jobs.vibrantm.com

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.merckgroup.com/en/company/press-positions.html

Job Requisition ID: 253821

Location: Singapore

Career Level: D - Professional (4-9 years)

Working time model: full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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