Lead or participate in laboratory equipment and computer software validation in accordance to site procedures and regulatory requirements, inclusive of writing, reviewing and approval of validation related documentations
Ensure that analytical equipment are maintained and calibrated accurately and timely in accordance to site procedures, corporate guidelines and regulatory requirements.
Maintain and support computer systems and laboratory equipment according to site change control and access control procedures.
Lead and/or participate in investigations arising from laboratory equipment/incidents and propose effective CAPA to minimize recurrence.
Requirements:
Degree in Science with experience in the field of Chemical, Pharma or Manufacturing industry Or Science diploma holder with extensive (>5 Years) experience in the field of Chemical, Pharma or Manufacturing industry
Good knowledge of GMP and laboratory equipment/validation
Good knowledge of quality, laboratory techniques and laboratory compliance
Good analytical and problem solving skills
Candidates with no prior experience will be considered
We regret that only shortlisted candidates will be notified. GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239
