Corestaff Pte Ltd – QC Lab Technician (Pharmaceutical Ind)

Company
Corestaff Pte Ltd
corestaff.com.sg
Designation
QC Lab Technician (Pharmaceutical Ind)
Date Listed
15 Nov 2023
Job Type
Entry Level / Junior Executive
Full/Perm
Job Period
Flexible Start, Permanent
Profession
Healthcare / Pharmaceutical / Sports
Industry
Manufacturing General / Biomedical / Pharmaceutical
Location Name
Tuas, Singapore
Address
Tuas, Singapore
Map
Allowance / Remuneration
$2,000 - 2,700 monthly
Company Profile

The company is a high-tech manufacturer of contact lens solutions, sterile pharmaceutical solutions, first-aid eye and wound irrigations as well as eye comfort drops. 

Job Description

QC Lab Technician (Pharmaceutical Ind / Entry Level)


Summary:

This individual is responsible for the supervisory of the microbiological testing to be done in accordance with relevant quality standards and regulatory requirements.

Responsibilities:

  • Perform and supervise all microbiological testing as required such as sterility test, total microbial count, particulate count, growth promotion test, gram stains, endotoxin test, environmental monitoring, etc.
  • Ensure all microbiological lab resources are utilized productively with lab goals and priorities.
  • Supervise the environmental monitoring program and ensure effectiveness.
  • Promote awareness with impacted departments on the control of the sterility assurance of the products and manufacturing processes.
  • Work with various departments on the expectation of the sterility assurance requirements of sterile product and prevent product contamination.
  • Continuously improve the lab practices by updating procedure and conducting training.
  • Support audits, validations, change control, product registration and preparation of relevant eports.
  • Conduct lab investigations and implement appropriate corrective/preventive actions.

 

Requirements:

  • Candidates must have the education in Diploma/Degree in Life Science (Microbiology, Biology, Biotechnology, Pharmaceutical).
  • Scientifically, materials, products and process evaluation or validation required by rules and regulations with relevant education and experience.
  • In-depth knowledge of the cGMP, 21 CFR Part 211, EU MDD/MDR and ISO 13485.

 

Lee Yuh Shiuan

Registration Number: R21101101

EA License No: 18C9027

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