Technologist, Laboratory

Edwards Lifesciences (Singapore) Pte Ltd; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A healthcare company in Singapore is seeking a qualified individual to perform laboratory tests and investigations. The role requires an Associate's Degree or equivalent with 3 years of lab experience. Candidates should have strong interpersonal skills, be able to communicate effectively, and possess excellent computer skills. Responsibilities include routine testing services, preparing reports, and assisting in equipment validation. The environment demands strict adherence to regulations regarding quality and safety.

Qualifications

• 3 years experience working in a laboratory environment required.
• Able to read, comprehend, write, and speak English.

Responsibilities

• Perform routine and non-routine testing services.
• Perform laboratory investigations and propose solutions.
• Prepare data summaries, reports, and protocols.
• Oversee the preparation of solutions.
• Assist with routine manufacturing equipment validation.
• Train and guide lower level technicians.

Skills

Excellent written and verbal communication

Interpersonal skills

Attention to detail

Education

Associate's Degree or equivalent in related science field

Bachelor's Degree in related science field preferred

Tools

MS Office

Analytical Equipment System (e.g. ChemStation, Empower)

Job description

Make a meaningful difference to patients around the world. At Edwards Lifesciences facilities around the world, our Manufacturing teams create the tools, technologies, and devices that transform patients’ lives. As part of our sewing, assembly, delivery, and distribution teams, your attention to detail and commitment to continuous improvement will help us turn innovative ideas into reality. Your purpose-driven work will help leave lasting and positive impacts on patient lives.

How you’ll make an impact:

• Perform routine and non-routine testing services by using established procedures/protocols (e.g. manufacturing investigations, D-value, B&F, FETS, glut, TLS, antimicrobial, sterility, in process solutions, etc.)
• Perform laboratory investigations and propose recommendations and solutions for manager approval
• Perform investigations on CAPA forms e.g., NCRs, RICA, OOT, OOS, for tests or processes nonconformance and identify root cause and propose corrective actions for manager approval
• Prepare data summaries, reports, and protocols using existing templates as a model as well as review and approve basic laboratory data and may propose recommendation on template changes
• Oversees the preparation of solutions
• Review, follow and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records
• Assist with routine manufacturing equipment validation by coordinating testing schedules and performing data analysis
• Propose and update operating procedures and ensure that specifications are in compliance with GMP, Environment and Safety regulations
• May train, coach, and guide lower level technicians on new procedures, assess work techniques and provide feedback on procedures
• Other incidental duties assigned by Leadership

What you'll need (Required):

• Associate's Degree or equivalent in Diploma in related science field, 3 years experience working in a laboratory environment required or
• Bachelor's Degree in Related science field preferred

What else we look for (Preferred):

• Excellent written and verbal communication, interpersonal, and relationship building skills
• Able to read, comprehend, write and speak English
• Excellent computer skills, including usage of MS Office; Analytical Equipment System (e.g. ChemStation, Empower) preferred
• Full knowledge of laboratory processes
• Full knowledge in QSR (Quality System Regulation), FDA (Food and Drug Administration), and ISO (International Organization for Standardization) regulations
• Full knowledge in mathematics, e.g., decimals and percentages
• Ability to write technical documents
• Strong knowledge with ISO microbiological sterilization documents (micro only)
• Strict attention to detail
• Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control