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Associate Scientist - Viral Clearance (Molecular)

 

A career at our company is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. 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 – Viral Clearance (Molecular) you will be part of the Process Solutions Services team that designs and delivers Viral Clearance validation studies for biopharmaceutical companies across the China region. In this role you will conduct a variety of tasks to support GLP/ GMP operations, perform qPCR endpoint assays to quantify virus titers, and maintain the testing laboratories and equipment in the validated state.  

 

You will be part of the lab testing team in Viral Clearance and carry out client studies with appropriate regulatory compliance under the oversight of the Study Director/Responsible Scientist.  As part of your daily responsibilities you will also initiate and support investigations, lead lab improvement projects, and generate SOP’s as required. The Associate Scientist will work closely with the scientists and laboratory personnel to execute client studies on time and right first time. 

 

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

 

Brief role description: 

  • Supports set-up of new facility and executes assay transfer and start-up of Viral Clearance lab operations 

  • Works within the Viral Clearance laboratories following Standard Operating Procedures (SOP) and relevant compliance regulations 

  • Performs qPCR assays to quantify virus titers and determine virus removal by client process unit operations.  

  • Authors/reviews assay report with qPCR results for studies; performs routine peer review of raw data records 

  • May perform cell culture and virus titration assays to ensure routine studies are completed on time  

  • May perform virus spiking, sample preparation and virus inactivation operations 

  • Accurately and promptly records data to meet appropriate scientific and GLP/GMP regulatory standards 

  • Performs investigations, handles deviations and owns CAPAs and change controls at site level  

  • Proactively implements continuous improvements to laboratory processes and procedures in accordance with 6S principles 

  • Coaches and trains junior team members on lab procedures and systems 

  • Carries out housekeeping and maintains material stock control in the laboratory as required 

  • 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 

  • Ensures equipment is maintained in the validated state and works with facility department to ensure timely implementation of periodic maintenance and calibration.  

  • Leads lab projects related to equipment validations, continuous improvement, CAPA’s, assay trending, etc 

  • Generates SOP’s and lab records as required 

 

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: 

  • Bachelor degree in Biological Sciences or higher degree in relevant scientific subject 

Experience: 

  • Minimum 2 years of experience in a regulated environment (GLP/GMP) 

  • Minimum 2 years of experience in a scientific laboratory role 

  • Prior experience in qPCR assays and demonstratable understanding of Molecular Biology 

  • Any of the following areas will be desirable: 

  • Prior experience in cell culture and/or virology  

  • Demonstrable scientific understanding in downstream bioprocessing (filtration & chromatography)  

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 

  • English fluency in speaking and writing. 

Core competencies: 

  • Safety and Quality 

  • Adheres to health and safety procedures and actively takes necessary action when encountering unsafe situations 

  • Is organized and pays attention to detail 

  • Adheres to SOPs and protocols, and ensures compliance to site policies and regulations 

  • Problem solving and drive 

  • Can learn new skills and knowledge quickly 

  • Uses logic to solve problems with effective solutions 

  • Enjoys working hard; is action-oriented and determined to provide best-in-class service 

  • Pursues everything with energy, drive and the need to finish, especially in the face of resistance or setbacks 

  • 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 

  • Is customer oriented and able to relate with clients from different cultures 

  • The ability to maintain effective working relationships with scientists and other lab personnel 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:  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!

 

Curious? Apply and find more information at https://jobs.vibrantm.com

 

Job Requisition ID:  219823
Location:  Shanghai
Career Level:  C - Professional (1-3 years)
Working time model:  full-time

Careers during Covid-19
Thank you for visiting our careers website, we are always looking for curious minds to join our teams. We understand how much the world is being impacted by the Covid-19 crisis and we want to assure you that your safety is very important to us. To ensure that everyone’s health is protected, instead of a standard face-to-face interview, it is likely that you will be offered alternative digital interview options.

US Disclosure
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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 HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday.


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