Search Results: 21 vacancies
...timely production of product with the quality and quantity in compliance with the relevant GMP, safety and environmental guidelines.... ...environment/equivalent
• Able to understand changing dynamics of Pharmaceutical industry
• Collaborating across boundaries
• Expertise in...
...the timely production of products with quality and quantity in compliance with the relevant GMP, safety and environmental guidelines.... ...environment/equivalent.
• Able to understand changing dynamics of pharmaceutical industry Collaborating across boundaries.
• Expertise in GxP...
...Education required: Bachelor of Science in Pharmaceutical Science/Chemical & Biomolecular (CBE)/Biological Sciences/Life Sciences or Bachelor... ...Ensure that the project execution activities are carried in a compliance manner to company policies and regulatory guidelines....
...Purpose
Responsible for sterility assurance programme and ensure compliance with company polices and current GMP expectations.... ...science or engineering
2. Min 5 – 7 years of experience in pharmaceutical industry especially related to aspects of sterility assurance...
...oversight of Supplier management activities on site to achieve compliance with company policies and government regulations as assigned.... ...regulatory and legal requirements as applied to quality assurance of pharmaceuticals manufacturing
User experiance with SAP will be prefered...
...teams.
Knowledge, Skills, and Experience
Min degree in mechanical or electrical engineering
Min 2 years of experience in pharmaceutical industry
Min 3 years of experience in troubleshooting instruments failure
Experience in GMP environment
Experience in preparing...
...Problem Solving
~ Good knowledge of MS Office suite of application especially MS Word, Excel and Powerpoint. Knowledge of cGMP for pharmaceutical manufacture. (Mandatory)
~ Knowledge on SAP system
~ Knowledge on Learning Management System such as Mylearning.
~ Pharma...
...Education required: Bachelor in Engineering, Biomedical Sciences, Chemical & Biomolecular Engineering and Pharmaceutical Engineering
Other requirements: Must be enrolled at a University for the duration of your Internship
Language requirement: Written and spoken fluency...
...discipline.
ITE in Engineering with at least 5 years of operation & maintenance experience of utilities systems or HVAC system in pharmaceutical industy.
Technically competent personnel with 6 - 8 years experience in maintenance activities.
Good experience and...
...ensure documents are ready for approval timely.
Be the administrator of the Site Document Management System and perform required compliance related checks for documents.
Issue controlled documents (e.g. Batch records, logbooks and sampling labels) in a timely manner, as...
...proper maintenance of QC IPC/DS (In Process control/Drug Substance) lab equipment and systems and troubleshoot to ensure full cGMP-compliance for shift team.
About the Role
Position Title : QC Analyst II
Location – Singapore #LI Hybrid
About the Role:
This role...
Summary
This role will maintain QC Raw Materials laboratory in full cGMP compliance.
About the Role
Position Title :QC Analyst IV - Raw Material
About the role :
About the Role:
This role will maintain QC Raw Materials laboratory in full cGMP compliance....
.../Equipmen , t QC) and implementation of Corrective and Preventive Action (CAPA)
Participate in cGMP self-inspections to ensure compliance with internal SOPs and regulatory requirements
Reporting/Documentation:
Operate key computer applications related to production...
...housekeeping is maintained.
Maintain awareness in SEHS within maintenance section.
Provide full support and accountability on compliance to SSOW system (eg. PTW, LOTO)
4. Quality
Ensure that all maintenance and repair/replacement activities are carried out in compliance...
...indicators (KPI) for the supply chain, especially for planning/provisioning monitoring
Ensure that routine audits are carried out in compliance with cGMP & authorized procedures and policies
Ensure timely maintenance of business master data (planning related) in a...
...on Good Documentation practices relating to archival
Be involved in deviation investigations if any
Support data collation and compliance sampling (documentation check) activities for the annual system effectiveness review
Support logistics and activities for audit...
...incubators
Liaise with external vendor for service quotation, escort vendor during service and approve invoice timely
Supports compliance activities:
Performs regular Ll audits in QC
Coordinates and supports all L2, L3 and L4 audits and the associated CAPAs...
...exceptions) and close the report on time.
Performs data trending and co-ordinates with relevant parties. Reviews QC reports to ensure compliance and promptness of results.
Problem solving
Identifies and reports problems in QC. Solve problems and implement corrective...
...compendial updates
Keeps up-to-date on regulations/ development of biopharmaceutical QC activities to ensure QC operations are in compliance to applicable corporate, regulatory and external agency regulations
Leads/ manages investigation of non-conformities (events and...
...trainees upon completion of the programme.
Purpose:
To be primarily responsible for the sterility assurance program and ensure compliance with company polices and current GMP expectations.
Key Responsibilities:
QA Oversight
Implement sterility assurance...
