Biotechnologist ( Shift *3/2/2/3* Contract To Perm, Gmp) Immediate

Singapore, Singapore

Job Description


Description



The job of a biotechnologist involves:

  • designing and implementing research studies
  • developing new research procedures
  • working with lab technicians on research
  • 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.

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Job Detail

  • Job Id
    JD1320660
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Singapore, Singapore
  • Education
    Not mentioned