Search Results: 19 vacancies
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal...
...lab equipment and systems and troubleshoot to ensure full cGMP-compliance for shift team.
Key Responsibilities:
• Perform product testing and analysis under cGMP to meet required timelines.
• Provide technical support to run and validate necessary test methods on lab...
...laboratory in full cGMP compliance.
Key responsibilities
• Lead raw material method validation/ verification and routine release testing
• Plan day to day operational activities in QCRM (i.e., housekeeping, release testing). Perform data entry, review and approval of...
...Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor
• Review and approval of analytical data / tests (analytical release) Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor -Documentation Specialist...
...skills? If so, this is the role for you.
As Quality Control Associates or Senior, you will be responsible for conducting sample testing of incoming materials and/or finished products to ensure compliance with regulatory agencies’ requirements and company standards....
...HVAC systems in a GMP environment.
Good experience and knowledge in electrical and process instrumentation matters.
Clean room testing, balancing and requalification.
Experience with EHS procedures e.g. risk assessments, permit-to-work etc.
Good interpersonal and...
...Site Name: Singapore - Tuas
Posted Date: Apr 2 2024
Purpose
To perform sampling/testing and support related activities in QC Biological team.
Responsibilities
1. Perform routine and adhoc/ non-routine testing in the following areas with good observation of...
...activities to assure timely availability and accuracy of results
Reviews and approves all required biochemistry/ microbiological testing for utilities, raw materials, environmental, manufacturing processes and products; ensures that the tests are analyzed in accordance...
...certificate will be given to successful trainees upon completion of the programme.
Purpose:
~ To provide technical support to routine testing teams in the frame of the Analytical Science and Technology (ASAT) team around method development/ qualification/ validation/...
...the chemistry laboratory activities to assure timely availability and accuracy of results
Review and approve all required chemistry testings for utilities, raw materials, manufacturing processes and products and ensure that the tests are analyzed in accordance with...
...following domains:
Bioburden & Endotoxin control
Aseptic process simulation
Sterile hold-time (SHT) & Container closure integrity test (CCIT)
Sterilisation methods, Vapourised hydrogen peroxide (VHP) decontamination
Changeover and Cleaning & disinfection
Aseptic...
...Responsibilities:
• Ensure all activities in compliance with cGxP, incl. data integrity
• Review and approval of analytical data / tests (analytical release)
• Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and...
...for Individuals
A certificate will be given to successful trainees upon completion of the programme.
Purpose:
~ To perform testing and support related activities in QC Biological team
Key Responsibilities:
Perform routine and adhoc/ non-routine testing...
