Senior Biotechnologist 1
2 months ago
As a Senior Biotechnologist at GSK, you will play a critical role in ensuring the production of bulk drug substances meets established timing and quality standards. Your expertise in bioprocess development and operations will be essential in maintaining good housekeeping of facilities and adhering to cGMP and safety requirements.
Key Responsibilities
* Adhere to cGMP and safety requirements
* Ensure good housekeeping of associated production facilities
* Identify areas for improvement and participate in continuous improvement projects
* Participate in commissioning and qualification activities
* Carry out other related duties as assigned by the N+1
* Provide guidance and leadership to ensure processes are completed reliably
Planning and Operations
* Follow day-to-day planning
* Assist in detailed team operations planning
Training and Development
* Ensure training and qualification in current effective SOP and OJT
* Engage in personal development and follow up on agreed development plan
* Provide guidance and support to new joiners
* Develop oneself as a process SME
* Guide junior employees to ensure knowledge transfer
Quality and Compliance
* Comply with all relevant SOP/Batch record requirements
* Perform timely review of documentation and make necessary corrections
* Have a good quality mindset and integrity
* Participate in deviation investigation process and implementation of CAPA
* Participate in cGMP self-inspections
Reporting and Documentation
* Operate key computer applications related to production function
* Ensure batch record, checklist, and logbooks are correctly recorded
* Maintain clear communication with N+1 and fellow colleagues
* Participation in development and generation of production checklist, SOPs, and validation protocols
Security, Safety, and Environment
* Awareness and adherence to site safety procedure
* Ensure safe operations on the field
* Identify and report potential safety issues
* Ensure proper housekeeping of assigned production areas
Interface with Other Departments
* Coordination with department colleagues to ensure timely supplies of materials and buffers
* Establish good working relationship with QA, QC, maintenance, and calibration
Requirements
* Min diploma in chemical technology, chemical engineering, or biotechnology engineering
* Min 2 years of experience in Biologics, Chemical, or Pharmaceutical industry
* Experience in working with GMP
* Familiar with purification/fermentation/conjugation/isolator operations/material and buffer operations
Preferred Qualifications
* Good team player and able to work independently
* Good communication and documentation skills
* Has disciplined and quality mindset
* Comfortable to work in a cleanroom environment
About GSK
GSK is a global biopharma company with a special purpose – to unite science, technology, and talent to get ahead of disease together. We prevent and treat disease with vaccines, specialty, and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology, and oncology).
Why GSK?
We want GSK to be a place where people feel inspired, encouraged, and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing.
Important Notice to Employment Businesses/Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site.
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