Join a global life sciences consultancy that values their employees
Work alongside experienced professionals and learn exponentially
Opportunity to work on complex projects
Our client is a client-focused life sciences consultancy that has a successful history in their service offerings. The company also puts great value on their employees personal and career development to ensure that they are providing top-notch services.
You will be responsible for:
Planning and adhering to qualification and requalification schedules
Preparation of Validation Plan, Commissioning Plan, and project procedures
Preparing and reviewing of FAT, Commissioning and SAT protocols
Preparing and reviewing of Qualification protocols (DQ, IQ, OQ and PQ)
Evaluating data from executed validation protocols
Generating or approving Validation Risk Assessment documents in relation to executed validation activities
Assessing and closing deviations related to closure of validation activities
Actively participating in relevant change control activities and risk evaluation systems as they pertain to validation
You have at least a Diploma/Degree in Life Sciences or Engineering field
You have at least 1 year of validation experience, ideally in FMCG, pharmaceutical, biopharmaceutical or medical device industry.
You possess knowledge of GMP facilities and cGMP requirements.
You have experience with Validation of facilities, utilities and process equipment
You pay strong attention to detail and deliver work of high standard
You are a strong team player who can manage multiple stakeholders
You are highly adaptable and can work well in changing environments
|Salary Range||SGD 4000 — SGD 8000 monthly|
|Experience Required||1 years|
|Employment Type||Full Time|
|Vacancies Available||1 available|
Headquartered in 1 RAFFLES PLACE #27-03 / Singapore
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