Senior Biotechnologist 1 (1-Year Contract)
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Job Location:
Monthly Salary:
Posted on:
12 hours ago
Vacancies:
1 Vacancy
Job Summary
As a Biotechnologist in our Value Streamyou will participate in the preparation operation and completion of assigned process stages to ensure the production of bulk drug substances is within establish timing and quality standards. You will also ensure good housekeeping of the facilities to keep them in good operational order in line with cGMP safety and environmental requirements.
Key Responsibilities:
Operations
Adhere to cGMP and safety requirements
Ensure good housekeeping of associated production facilities so that they are kept in good operational order
Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiency
Participate in commissioning and qualification activities as required
Carry out other related duties as assigned by the N1
Assigned as in-charge by process/operations area to provide guidance/leadership to ensure processes are completed reliably
Planning
Follow the day-to-day planning
Assist Lead Biotechnologist or Shift Supervisor or Operations Superintendent in detailed team operations planning
Training & Development
Ensure that he/she is trained/qualified in the current effective SOP and OJT in accordance with the assigned training curricula prior to commencing operation.
Proactively engage N1 to discuss personal development and follow up on agreed development plan.
To provide guidance and support to new joiner ensuring his/her smooth transition to the new environment
To develop oneself as a process SME
Guide junior employees to ensure knowledge transfer for business continuity.
Conduct classroom and on-the-job (OJT) training as assigned.
Quality
Comply with all relevant SOP/Batch record requirements.
Perform timely review of documentation and make necessary corrections.
Have good quality mindset and integrity to ensure products are manufactured with the highest quality
Participate in deviation investigation process (Process Environmental Maintenance/Equipment QC) and implementation of Corrective and Preventive Action (CAPA)
Participate in cGMP self-inspections to ensure compliance with internal SOPs and regulatory requirements
Reporting/Documentation
Operate key computer applications related to production function
Ensure that batch record checklist and logbooks are correctly recorded cGMP complied and maintained
Maintain clear communication with N1 and fellow colleagues providing clear feedback of any items pertaining to safety quality and efficiency
Participation in development and generation of production checklist SOPs validation protocols and the regular review and updates of these documents
Perform VS review of completed documentation to ensure adherence to GDP
To lead design/drafting of working instruction to ensure that it is user friendly to improve GDP
Technology Transfer
Participate in new technology and/or new process transfer
Security/Safety/Environment
Awareness and adherence to site safety procedure.
Ensure safe operations on the field
Identify and report all potential safety issues (personal protection requirement equipment protection way of working etc).
Ensure proper housekeeping of assigned production areas to minimize safety hazards
Participate in Safety Inspections
Participate in Workplace Risk Assessment
Interface with other Department/Team
Coordination with department colleagues to ensure
Timely supplies of materials and buffers
Calibration/maintenance activities are supported.
Open communication on sampling requirements to QC department
Establish good working relationship with QA QC maintenance calibration to ensure smooth operations.
Basic Qualifications
NITEC/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
If you have the following characteristics it would be a plus:
A 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.
To learn more about Singapore GSK and our people please click on this link: GSK
Uniting science technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.
People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.
We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities contact . Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.
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. All employment businesses/agencies are required to contact GSKs commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Required Experience:
Senior IC
Key Skills
- IVR
- SOAP
- Avaya
- Solaris
- Cost Accounting Standards
- Database Design
- Hibernate
- ITIL
- Weblogic
- Express.js
- Contracts
- ASP
About Company
About us We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.
