setting up the laboratory equipment to conduct and monitor experiments
collecting, studying and testing samples such as food, cells, tissues, blood samples, bacteria cultures and living organisms
recording findings and analysing the results
identifying how the research can be applied to improving human life
you are responsible in:
create, conduct and monitor experiments using live organisms or bimolecular processes in a laboratory setting to solve problems, improve processes and develop new products
use scientific knowledge to follow different methodologies to achieve results
perform data analysis on your experiments and interpret findings to support scientific investigations
record and disseminate results accurately in reports and via presentations
set up, maintain and operate standard laboratory equipment and computers
work independently and collaboratively with other scientists
work to health, safety and environmental regulations and meet quality standards
keep up to date with new advances in biotechnology to develop new techniques, products or practices.
Job Requirements * Degree in Chemical Engineering / Bioengineering / Chemical & Biomolecular Engineering / Pharmaceutical Engineering or related and possess 0 - 2 years of relevant experience in the biotechnology or pharmaceutical industry
Diploma in Applied Chemistry / Biomedical Sciences / Chemical Engineering / Food Science & Technology / Biologics & Process Technology / Chemical & Pharmaceutical Technology/ Food Science & Nutrition / Molecular Biotechnology / Biotechnology / Chemical & Biomolecular Engineering / Pharmacy Science or related and possess 2 - 4 years of relevant experience in the biotechnology or pharmaceutical industry
Nitec in Biotechnology / Chemical Process Technology or related with 4 - 6 years of relevant experience in the biotechnology, pharmaceutical industry
Will work holidays and overtime as required
May be required to adjust work schedule to meet production demands
**GMP experience** will be an advantage
The individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Electronic Batch Records (EBM), Batch Records and Forms.
Primary responsibilities include:
80%
Perform routine and non-routine production operations as per SOPs
Execute instructions and record data in the Electronic Batch Management (EBM) system
Perform Clean-In-Place (CIP) /Steam-In-Place (SIP) activities as per MFR/SOP
Perform filter integrity testing (FIT)
Perform filtration and filter management as per SOP
Attain good operating knowledge of the Process Control System (PCS)
Attain good operating knowledge on the Manufacturing Execution System (MES)
Perform equipment cleaning as per SOP
Perform equipment monitoring
Perform scheduled cleaning of equipment
Acquire good knowledge in handling of consumables (e.g. Bottles, filters, autoclave assemblies, etc.)
Perform laboratory tasks including but not limited to sampling, pH and conductivity measurements (If required), identify and report if there\'s any atypical events
Pursue on-the-job training through Competency Assessments to increase knowledge and understanding
Record data into logbooks, log-sheets and forms (If applicable)
Responsible for Alarm/Alert review and real time trouble-shooting
Responsible for logbooks and log-sheets review and follow up
Perform troubleshooting and resolve process related issues
To participate and resolve process related issues (If required)
Support transfer of new processes, commission or validation of new project
Collaborate with other departments to resolve issues related to daily operations
Training of new team members.
Demonstrate good cleanroom technique in the handling of product and materials
Coordinate in-process sampling and submission
Mentor and perform On-Job-Training to team members
Support GMP and Safety audits (If required)
Perform 5S housekeeping
Support transfer of new processes and commission/validation of new projects (If required)
Carry out work in a safe manner, notifying management of safety issues and risks
Involve in hands-on execution of the plant operations and assist Supervisors in trouble-shooting
Actively participate in continuous improvement initiatives
Perform components staging for autoclaving and parts washer
Perform assembly and disassembly of process equipment
Perform parts washer operation as per SOPs
Perform loading and Operating of Autoclave
Responsible for MFR (Manufacturing Formulation Record)/SOP creation and revision
Perform monitoring for process and equipment performance during operation as per SOP/MFR, identify and report if there\'s any atypical events
Support investigation to event and deviation
Interface with other departments to resolve issues related to daily operations
Actively support transfer of new processes and commission/validation of new projects
Actively support Change Control management
10%
The individual will manage equipment and support facility related projects by
Support routine safety and GMP walk down and responding to findings (If required)
Support execution of Corrective/Preventive actions which identified (If required)
Support change control activities which assigned (If required)
Act as a SME for investigation and solution
Liaise with other department for Corrective/Preventive actions which identified
Support shift change/handover activities
10%
Staff Technical Training and Development
Meet and maintain training requirements
Complete assigned training on time
Provide technical training for area personnel
Provide input on training material development
Deputize for shift supervisor\'s activities
Provide annual performance self-assessment on development plan
Responsibility to adhere to any applicable EHS requirements.
Commitment to a fair and respectful relationship to others and behavior in accordance with Code of Conduct.
Education and Experience Requirements
Min Degree in Biomedical Sciences / Chemical Engineering or related with up to three years of relevant experience in the biotechnology, pharmaceutical industry
Min Diploma in Applied Chemistry / Biomedical Sciences / Chemical Engineering / Food Science & Technology / Biologics & Process Technology / Chemical & Pharmaceutical Technology/ Food Science & Nutrition / Molecular Biotechnology / Biotechnology / Chemical & Biomolecular Engineering / Pharmacy Science or related with minimum two years of relevant experience in the biotechnology, pharmaceutical industry
Min Nitec in Biotechnology / Chemical Process Technology or related with minimum five years of relevant experience in the biotechnology, pharmaceutical industry
Knowledge of plant and unit operations (autoclave, parts washers, COP and SIP systems)
Demonstrate commitment to cGMP, EHS compliance aspects of clean-room and plant operation
Experience in ERP/MES/control systems applications will be an added advantage
Able to take initiative with good problem solving skills
Excellent team player with hands-on attitude
Able to work on rotating shifts
Able to support overtime as required
Able to support production demands with adjusted work schedule
Adhere to all EHS/GMP requirement
Ability to wear appropriate PPE/Cleanroom gowning as per SOP
Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas.
Ability to lift, pull or push equipment requiring up to 20kg
Able to climb ladders and work on platforms
Able to perform confine space entrant/attendant/Supervisor/Assessor (If required)
Ability to read/understand Safety Data Sheet (SDS) and handle chemicals as per SOP
Able to monitor and analyze processing parameters to identify atypical trends
Able to support Continuous Improvement Projects
Able to perform as a subject matter expert for equipment and/or systems
If you are interested in any of the positions, do kindly drop your most updated resume to recruithealth@recruitexpress.com.sg (Attn: Biotechnologist)
Industry
Education & Training Healthcare / Pharmaceutical / Life Science / Medical Device Semiconductor / Electronics / Engineering
Specialization
Chemist / Research Scientist Engineering Healthcare - Pharmaceutical / Life Science / Medical Device / Clinical Research / Regulatory Affairs
Location
Central, North, East, West
Employment Type
Contract / Temp Permanent
Salary
Negotiable
If you meet the requirements of this role, please email a detailed resume in Word document to Leon Leong De Cong. CEI Registration No.: R1551708 Email: recruithealth@recruitexpress.com.sg
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.