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SalaryAbout us
GMP Pharmaceuticals, one of the leading contract manufacturing company specialised in healthcare supplements and TGA listed products that embraces the culture of professional and personal growth, collaborative partnership and exceptional diversity in world-class facility built to pharmaceuticals and international GMP standards. We have grown into one of the largest organisations in the industry and serving many clients both locally and in over 30 countries around the world. Our teams of qualified experts dedicated professional and hard-working individuals are committed to deliver outstanding quality and innovative products through research and development, discipline, and innovative thinking.
The role
Our Quality Control team is eager to welcome an experienced and passionate QC Analyst to join the team at our Head Office in Huntingwood. The role focuses on delivering high standard QC testing, validation processes on materials and products and carry all ranges of QC lab responsibilities on daily basis.
The key responsibilities for the include but are not limited to:
- Perform routine analysis which includes physical tests and chemical tests as per applicable Analytical Test Methods or Pharmacopoeia for raw materials and finished products.
- Analyze and document QC work by using basic instrumentation and instrumentation with advanced software in accordance with SOP, GMP and GLP. Performing wet chemistry analysis when required.
- Assist in ensuring the requirements of TGA, NSW Food Authority or any relevant regulator as applicable.
- Ensure all analytical works strongly interlinks with data Integrity.
- Maintain accurate laboratory records for all testing, analytical work, and investigations.
- Assist in the handling of Out of Specification results and further investigations.
- Maintain adequate stocks of standard, chemical and consumables
- Calibrating and maintaining laboratory equipment
- General housekeeping and maintaining WH & S
The ideal candidate has the following qualifications and experience:
- Bachelor of Science or higher in science field with over 1-2 years relevant experience
- Experienced working in a TGA or NATA licensed laboratory (Desired)
- Basic instrumentation knowledges with the ability to apply without advanced software e.g. Karl Fisher, Auto titrator, Hardness Tester, Disintegration Tester, Viscometer, Polarimeter, Sieve shaker, Tapped density and InfraRed. Instrumentation with advanced software i.e. UV spectrophotometer, Inductively Coupled Plasma, HPLC, UHPLC, GC.
To be successful in this role we are seeking the following additional skills and attributes:
- High level of accuracy, technical capability and attention to detail
- Ability to manage time to ensure testing/activities are completed in a timely manner
- Excellent oral and written communication skills
- Working knowledge of QC processes, systems, and methodologies
- Ability to build and maintain strong working relationships with all levels of the organization
- Problem solving ability and passion for quality outcomes
- Ability to multitask and work autonomously as well as in teams
- PR/Citizen highly desired.
What are the benefits:
- Working with a supportive team
- Experience working with an innovative company
- Variety of Modern equipment to utilise or learn
Job Types: Full-time, Permanent
Salary: $55,000.00 – $60,000.00 per year
Schedule:
- 8 hour shift
COVID-19 considerations:
All employees are required to conduct RAT Test once in a week.
Application Question(s):
- How many years' experience do you have in a quality control (QC) role?
- Please describe your working right in Australia
- Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?
- How much notice are you required to give your current employer?
- What's your expected annual base salary?
Experience:
- testing Analyst: 1 year (Preferred)
