Qc In-coming

17 hours ago


Singapore GMP Group Full time

**QC In-coming & Process Validation Manager**

Our client is the renowned manufacturer and supplier of medical & healthcare products in Singapore. They are committed to enhance the quality of life through constant product innovation and quality enhancement. Join them to take pride of what you can do to improve people’s life.

***

**Responsibilities**:

- To be responsible for leading the QC team working towards total quality management of products (from in-coming raw materials to finished products).
- To take ownership of all quality related incidents, CAPA, GMP documentations, and follow-up actions.
- To support and ensure all equipment, devices, and instruments (new or existing) are qualified, validated, calibrated, maintained, and operating in accordance to specified standards and requirements.
- To ensure environmental monitoring (EM) is properly performed, monitored, and trended in accordance with quality/ safety requirements.
- To support manufacturing validations, trial studies, change controls, product recalls and dispositions.
- To carry out GMP/ GDP/ safety and quality related trainings whenever needed.
- To initiate or support quality control related process improvement projects.

**Requirements**:

- Minimally with a degree in Chemistry, Pharmaceutical, Material Science, Bioscience or equivalent.
- Minimally 5 years of in-coming and in-process quality control related working experience (including validations) in the pharmaceutical/ biotech/ healthcare products or cosmetic industries.
- Good knowledge of Good Manufacturing Practices (GMP), Good Documentation Control (GDP) and ISO standards and regulations.
- Practical experience in equipment qualification & validation is an advantage.
- Detail oriented.

To find out more about this opportunity, please contact
- GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Patricia Lin | Registration No: R22105276


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