Dynalynk Pharma Pte Ltd – QA and QC Officer

Company
Dynalynk Pharma Pte Ltd
lynkbiotech.com
Designation
QA and QC Officer
Date Listed
15 Nov 2023
Job Type
Entry Level / Junior Executive
Full/Perm
Job Period
Flexible Start, Permanent
Profession
Sciences / Laboratory / R&D
Industry
Manufacturing General / Biomedical / Pharmaceutical
Location Name
Lorong 21 Geylang, Singapore
Address
Lor 21 Geylang, Singapore
Map
Allowance / Remuneration
$1,600 - 2,200 monthly
Company Profile

Founded in July 2006, DynaLynk Pharma is a subsidiary of local pharmaceutical company Lynk Biotechnologies Pte Ltd.  It is located in a prime area that has been designated as the biomedical manufacturing hub of Singapore.

DynaLynk Pharma is the latest high-tech investment undertaken by local pharmaceutical company Lynk Biotechnologies, further expanding the Lynk Group’s competencies from its traditional domains of R&D and product development into the pharmaceutical manufacturing arena.  DynaLynk Pharma lends manufacturing capability to the Group’s thrust in commercialising locally-generated intellectual property, enabling the Group to meet business growth needs worldwide. 

DynaLynk Pharma’s rigorous quality systems, state-of-the-art equipment and facilities, as well as a commitment to excellence place it in a prime position to offer its valued partners reliable, responsive and specialised contract manufacturing solutions.

Job Description

Responsibilities:

  1.  To perform daily sampling of water and perform pH and conductivity testing.
  2. To perform sampling on incoming raw material, packaging material and detergents.
  3. To perform quality inspection on packaging materials.
  4. To perform in process testing.
  5. To assist in collection of samples for cleaning validation.
  6. To perform qualification of pH meter, clean booth and weighing balances.
  7. To ensure the safe keeping of retention samples of raw materials and finished products, and monitor the humidity and temperature of retention room.
  8. To liaise with contract laboratory for testing of materials.
  9. To coordinate the release of starting materials, packaging materials, finished products and detergents.
  10. To perform other ad hoc duties as assigned.

Requirements

  1. Diploma holder in relevant QA discipline, Analytical Chemistry, Chemistry, Pharmaceutics or related sciences or equivalent.
  2. Experience in GMP documentation/ reporting are preferred.
  3. Meticulous, driven and resourceful with excellent people skills
  4. Knowledge of qualification / validation is preferred

Please provide the following:

  1. Reasons for leaving past & present employment
  2. Last drawn/current and expected salaries
  3. Your earliest availability
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