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Responsibilities:
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Batch release of finished products.
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Ensure every released batch is compliant to relevant GMP standards and Marketing Authorizations.
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Supervise manufacturing, quality control and quality assurance activities for compliance to relevant GMP standards.
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Participate in validation, deviations, change controls, CAPA and quality risk management activities.
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Ensure self inspections are carried out according to established procedures.
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Other duties assigned by management.
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Occasional travel may be required.
Requirements:
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Registered Pharmacist in Hong Kong with valid Practicing Certificate issued by the Pharmacy and Poisons Board of Hong Kong.
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Minimum 3 years related work experience in GMP pharmaceutical manufacturing or quality control.
- Familiarity with sterile products manufacturing and/or PIC/S GMP would be an advantage.
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Good command of spoken and written English and Chinese; Putonghua is an advantage.
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Immediately available is preferable.
Interested candidates, please forward your resume in WORD format to
[email protected]
quoting reference 'n0423' in the subject line
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