QA Specialist

9 hours ago

Singapore GMP Group Full time

**QA Specialist**

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 prepare and update all quality related documents (SOP, Work Instructions, Quality Manual, Standards, Specifications, Forms, Reports & etc.).
- To ensure all GMP documents are maintained in accordance with regulatory requirements.
- To actively participate in the process deviation assessment, investigation, CAPA actions & closure.
- To provide quality related technical inputs during audits (internal & external).
- To handle and support supplier quality related complaints, recalls and audits.
- To ensure quality compliance of all tests, trial runs, stability studies, equipment qualifications & validations.
- To assist QC manager in conducting GMP/ GDP training, reviewing and disposition of incoming material when needed.

**Requirements**:

- Minimally with a diploma in Chemistry, Pharmaceutical, Material Science, Bioscience or equivalent.
- Minimally 2 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), FDA and ISO standards and regulations.
- Ability to communicate with Mandarin speaking suppliers in China is an advantage.

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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