Prepare QA and QC documents in accordance with quality management standards and external regulations
Assist in internal audits and batch manufacturing and packing records checks in accordance with cGMP standards on production batches to ensure product quality
Maintain quality manual and SOPs for quality procedures, and assisted in creating new procedures and SOPs where required
Maintain quality records such as batch manufacturing and packing records, monitoring, testing, and validation records
Assist in all quality audits and inspections conducted by local and foreign health authorities
Work with various teams to develop a statement of work.
Maintain proper inventory control
Any other tasks as assigned
Requirements
NITEC /Degree /Diploma in Pharmaceutical Science and above or equivalent.
Minimum 3 years of relevant experience.
Computer-literate (i.e., Word, Excel, PowerPoint)
Excellent communication and interpersonal skills
Competitive remuneration package will be offered to the shortlisted candidate.
Interested candidates, please send your updated CV in MS Words format stating your last drawn salary, expected salary, notice period and reason for leaving last / past employment(s) and email to recruit@caed.com.sg for priority processing.
To find out more job opportunities, visit Career Edge Asia at www.caed.com.sg for all job listings.
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Attn: Jace Tay (Registration No.: R1331152)
CAREER EDGE ASIA PTE LTD EA Licence Number: 13C6678 To find out more job opportunities, visit Career Edge Asia at www.caed.com.sg for all job listings. Email: recruit@caed.com.sg