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Staff. QC Physics
Terumo BCT Viet Nam · Đồng Nai
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Loại hình
Toàn thời gian
Hình thức
Tại văn phòng
Cấp bậc
Nhân viên
Ngành nghề
Sản xuất
Mức lương
Thương lượng
Địa điểm
Đồng Nai, Đồng Nai, Đồng Nai
Tổng quan
- Follow technical and administrative work such as checking, receiving and
- registration of samples, sorting of samples to the test areas, tests carried out
- are according to the method specified, results are precise and accurate, and
- tests are completed as per sample priority and due date, accurate data entry
- generating the reports, and timely delivery of results and reports, without
- compromising on the quality, accuracy and procedures.
- Be responsible for routine/non-routine QC Functional Laboratory analysis of
- finished products, process validation, Investigation, NC/CAPA. The candidate
- must demonstrate experience working in a cGMP laboratory and possess
- basic knowledge of industry regulations related to pharmaceutical and medical
- device manufacturing. Assist senior staff in method validation and method
- development.
- Check, receive and register of samples, sorting samples to the test areas.
- Prepare testing samples, solutions, standards and reagents to support testing.
- Perform functional analysis under the direction of senior staff with compliance
- to the procedures and standards, under the direction of senior staff with
- compliance to the procedures and standards, with timely delivery as per
- sample priority or due date, without compromising the quality and accuracy.
- Able to perform other testing upon completion training of test methods and
- Verification of Effectiveness (VOE) of QC Microbiology and QC Chemistry
- Team.
- Have analytical skills in the maintenance, operation and interpretation of the
- results obtained from analytical instruments.
- Perform routine maintenance activities in the laboratory and participate in the
- qualification and periodic calibration of equipment.
- Perform training for entry level staff and peer-to-peer training.
- Identify and troubleshoot problems with instrumentation and analytical
- preparations.
- Assist senior staff for the execution of method validations, qualifications, and
- transfers.
- Assist with Lab OOS/NC/CAPA Investigations in his/ her area.
- Able to perform review of all worksheets and logbooks.
- Conduct supporting duties such as wash and dry apparatus and vials and
- reject and discard samples.
- Support in inventory of spares, gases, chemicals, consumables etc. to ensure
- no incidence of zero stock level.
- Record any verifications, maintenance and calibration or repair works in the
- respective equipment logbook.
- Practice 5S and conduct self-audit as per sectional audit checklist.
- Maintain filing records as per record management retention schedule by filing
Quyền lợi
Đào tạoCổ phần / ESOP
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