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West Pharma Sr QC Technician Jurong Singapore, Singapore 651198954
17.04.2025
Job Summary
In this role you will be responsible to independently provide analytical review of the data generated for internal and external customers as well as supporting post-production related Quality activities such as finished batch release, including sterilization, packaging specifics, work order approval and support additional quality department activities. This position also requires maintaining knowledge of the current local and/or International regulations/guidelines/policies applicable to West's products and services.
Essential Duties and Responsibilities
- Perform cGMP Data Review on the analytical data generated in Lab Operations which may include raw materials and finished goods, product performance, container closure integrity, particle analysis, and/or microscopy/investigation
- Review the analytical raw data generated by laboratory operations according to established methods, protocols, Compendia and Work Instructions for cGMP compliance
- Review Electronic Data and Audit Trails for data integrity compliance
- Review Lab Operations Methods, Protocols, and Work Instructions for cGMP Compliance
- Responsible to review and approve of samples and / or batch release including review and approval of the finished Device History File documentation and Certificate of Compliance issuing.
- Responsible to review and approve of relevant packaging and respective graphics artwork
- Maintain working knowledge of computer software packages including MS Office suite, Adobe, MasterControl, LIMS, and LMS
- Collaborate as needed on proposed path forward regarding documentation questions
- Support preparations for periodical management reviews
- Initiate processes in SAP as needed related to finished batch release and sterilization processes
Additional Responsibilities
- Provide a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
- Maintain a clean, orderly, and safe workstation and environment at all times.
- Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
- Exhibit regular, reliable, and punctual attendance.
- Perform other duties as assigned based on business needs.
- Keep current with new GMP compliance guidance and internal QA procedures
- Support new GMP compliance guidance and Data Integrity initiatives
Education
- Bachelor's Degree Technical Studies or Science or equivalent experience preferred
Work Experience
- 0-3 years of experience required and
- Minimum 2 years of cGMP experience preferred
Preferred Knowledge, Skills and Abilities
- Able to be aware of all relevant standard operating procedures as per Company policy
- Support and contribute to Lean Sigma programs and activities towards delivery of the set target
- Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude
- Willingness to learn new and review new analytical techniques
- Meet individual and departmental goals as required
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
- Ability to learn, understand, and remember normal tasks.
- Ability to hear, speak, and understand conversation in English.
- Must maintain the ability to work well with others in a variety of situations.
- Must be able to multi-task, work under time constraints, problem solve, and prioritize.
- Read and interpret data, information and documents
- Work under deadlines with constant interruptions
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