Pharmaceutical Technician (Production Support, Drug Substance or Drug Product)
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Esco Lifesciences Group provides enabling technologies, products and services to the life sciences and healthcare industries, supporting academic research and scientific discoveries, clinical practice, as well as biopharmaceutical R&D and manufacturing. Headquartered in Singapore, Esco has an extensive sales network in over 100 countries, direct sales and service offices in over 24 countries, 8 manufacturing and R&D hubs in the US, Europe, the UK, China, Singapore, Indonesia, and over 1500 employees worldwide.
Esco is poised to benefit from the sustained growth of the healthcare and biopharma industries in Asia and globally. Esco has achieved market leadership in China, and globally, in multiple categories within some of the fastest-growing segments — with China being its largest and fastest growing market. As a Singapore-headquartered company, Esco is a nexus of East and West, bridging technologies, products and talent across the world, with global operations spanning the US, Europe and Asia.
You will be part of Esco Aster’s Manufacturing team and contribute to the overall site mission and objectives. You will ensure pharmaceutical operation activities and tasks are planned and executed in an efficient and compliant manner, while adhering to cGMP standards. You will work with the Leadership team of Manufacturing to develop a continuous improvement mindset and engage in teamwork with cross-functional departments.
We are looking for someone equipped who has excellent organizational skills and the ability to prioritize their workload to be part of our plant start up team.
Primary work location: Ayer Rajah Crescent, Singapore
Safety
- Foster
a safety-first mindset and adhere to company safety policies/procedures
- Identify
and report potential safety issues or near-misses/hits
- Support
the development of workplace safety risk assessments
General
- Perform
activities that can include periods of rigorous, repetitive work
- Work
in a cleanroom environment, wearing steel toe shoes, full clean room
gowning, hairnet and gloves when performing all work
- Maintain
an organized and clean workspace
Quality
- Always
ensure strict adherence to cGMP requirements.
- Follow
GMP documents (SOPs, Batch Records) with strict adherence to safety and
compliance
- Complete
documentation (e.g. batch records, logbooks, deviation reports) following Good
Documentation Practices / ALCOA principles
- Author,
revise or review documents (e.g. SOPs, BRs and Logbooks)
- Perform
timely review of documentation
- Support
deviation investigation and implementation of CAPA
Operations
- Support
process / equipment commissioning or qualification activities
- Operate
process and analytical equipment per defined standard operating procedures
(SOPs)
- Perform
critical processes and in-process sampling per defined Batch Records (BRs)
- Ensure
good housekeeping of production facility and equipment
- Adhere
to daily production schedule
- Report and discuss with supervisors
regarding any problem arising during the manufacturing process, which may
lead to stoppages.
- Ability
to perform basic troubleshooting
- Identify,
recommend, and implement improvements
We are
seeking individual with unique experiences in the respective fields and are also
providing unique learning/training opportunities as well:
Production Support
- Perform production activities, including
set-up, operation for the following, but not limited to:
- Buffer and media preparation
- Manual Cleaning
- Filter Integrity Testing
- Autoclaving
Drug Substance
- Perform production activities, including
set-up, operation for the following, but not limited to:
- Aseptic
processing in Isolators and Biosafety Cabinets
- Mixer
Tanks
- Incubators
- Perform
in-process sampling and monitoring of cell culture process
Drug Product
- Perform production activities, including
set-up, operation for the following, but not limited to:
- High-speed filling machines
- Isolators
- Compounding tanks
- Dispense, compound, and fill active
biological product.
- Perform in-process sampling on semi-finished
drug products
- Perform visual inspection, labeling and
packaging on semi-finished drug products.
- Higher
Nitec or Diploma in Biotechnology/Chemical/Mechanical Engineering and/or
Life Sciences and/ or Biology
- Minimum
2 years of working experience in pharmaceutical manufacturing.
- Good
knowledge in applying regulatory guidelines especially in manufacturing
process
- Experience
in a start up environment will be a plus
- Possess
a continuous learning mindset
- Able
to work in teams to complete operational tasks
- Able
to maintain good working relationships with QA, QC and Engineering.
- Able
to regularly lift up to 10 KG, push and pull objects that require up to 20
KG of force, and work on your feet for long durations
Apply now by submitting a Cover Letter and CV to [email protected].