Average salary: SG$6,500 /monthly
More statsSearch Results: 37 vacancies
...Technical Area Sales Manager
About HMT
HMT was founded in 1978 with the objective of providing better technology to the aboveground storage tank market. HMT's founders created products which not only solved the emissions problems of the day but also eliminated the operational...
...Individuals
A certificate will be given to successful trainees upon completion of the programme.
Purpose:
To be responsible for managing the interactions with third party organisations that supply QA incoming materials and/or services to GSK.
To manage material...
4700 SGD
Job Summary:
As a Commercial Manager in Index Cool Design & Furnishing, you will provide crucial support in handling the commercial aspects of shipyard and any incoming projects, including assisting with quotations, project costings, and contract management related to *Carpentry...
Index-cool Design & Furnishing Pte Ltd
Tuas, Singapore Country
19 days ago
...bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site... ...supervision of the Quality Systems Lead and have the opportunity to manage the archival system for GMP documents on-site. During the...
...bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site... ...MSAT) in the company to provide appropriate and timely inputs.
Manages QC projects related activities and to provide support to ensure...
...bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site... ...the news
What will you do?
Where does the role fit?
Manage administration of all Environmental, Health & Safety (EHS)-related...
...bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site... ...What will you do?
Be the assistant to the Sustainability Manager at the Sustainability Council Meeting
Be the key person to promote...
...bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site... ...?
Where does the role fit?
~ Support the operations team in managing the daily production activities, including maintaining general...
...bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing site... ...and confidence to trust your own judgment
Great project management skills and the ability to prioritise
What do we offer you?...
...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...
...manufacturing facility which includes process, utilities, building services, electrical and instruments
Support GSK Work Package Managers in detailed specifications/designs for the fabrication/ purchase of all plant and equipment and work across engineering disciplines...
...to meet customers specifications
Work with relevant agencies to adhere to certification requirements when required
Work with management to establish/ maintain company’s QMS and is Management Representative (MR) of company
Work with Procurement/ Purchasing to ensure...
...deliver its operational objectives. Areas of support includes process optimization, validation activities, continuous improvement, change management, deviation investigation and production project management to ensure that Value Stream can operate optimally and in compliance with...
...regulatory requirement, and GMP practices/ procedures in place and in use within GSK Tuas.
Responsibilities
General Project Quality Management
Ensure quality-by-design in all aspects and stages of the project is in alignment with the defined Project Quality System and...
...GMP team in day-to-day activities and work on improvement projects.
You will be required to:
Scan and archive of Batch Records
Manage GMP checklists/ reports from the QA GMP and Batch Release team. These include but not limited to the Post Production Batch Record...
...skills (preferably with "legible" handwriting)
5. Good interpersonal skills
6. Planning and organising skills (for individual time management & work planning)
7. Team Player
8. Leadership and problem-solving skill with analytical and logical thinking
9. Fair command of...
...in a GMP environment
• Experience in Raw Material Lab and Method validation
• Handling quality metrics & issues Knowledge of GMP Management of Quality Audit, Quality Change, Control Good Documentation
Why consider Novartis?
236 million lives were touched by Novartis...
...understand changing dynamics of pharmaceutical industry Collaborating across boundaries.
• Expertise in GxP operations. Operations Management and Execution.
• Associate to work on 12hrs rotating shift work in Downstream Process.
Desirable Requirements:
• Working...
...regulatory requirements.
Provide input on aspects relating to Sterility Assurance for qualification and validation strategies.
3. Management & Planning
Proactive and timely engagement of internal or external stakeholders, as necessary
Engage the necessary...
...Essential Requirements:
• 3+ years of experience in pharmaceutical quality control, quality assurance or production
• Operations Management and Execution; Functional Breadth; Collaborating across boundaries; Applied Practice
• Collaboration; result-oriented. Good...
