Quality Control Analyst Pharmaceuticals

Founded in 1994, GMP Pharmaceuticals has been focused on health supplement manufacturing for over 25 years. We are a TGA, Medsafe, FDA and GMP licensed complementary healthcare manufacturer with facilities in Australia and New Zealand and offices in China. GMP not only contract manufactures and packs a wide range of dietary supplements and functional food products, we also offer a broad range of services including product fomulation, label design, packaging solutions, shipping and regulatory advice across multiple regions. Our ability to provide end-to-end solutions for our clients makes us your one-stop quality health food manufacturer.

Quality Control Analyst - Pharmaceuticals
Private Advertiser


The Company
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 cGMP standards. 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 fast-growing Quality Control team is eager to welcome an experienced and passionate QC Analyst to join the team based in Western Sydney. 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.
Primary Responsibilities:
To prepare master documents for laboratory e.g. SOP, Analytical Test Procedure, Analytical Test Worksheet, Excel Calculation Worksheet.
Plan Analytical Method Validation and process validation as per regulatory requirements.
Coordinate with QA for QMS Documents e.g. OOS, Change Control, CAPA.
Monitor/Update laboratory instrument calibration and preventive maintenance schedule.
Coordinate with laboratory instrument and consumable suppliers for better functioning of laboratory.
Assist in ensuring the requirements of TGA, NSW Food Authority or any relevant regulator as applicable.
Ensure that the analytical work of QC strongly interlinks Data Integrity.
Maintain accurate laboratory records for all testing, analytical work and investigations.
Ensure that laboratory related safety issues are raised to company awareness and resolution.
Review of QC analytical data for raw material and finished products.
Other Responsibilities:
Assist in the calibration and maintenance of laboratory instruments and equipment.
Providing SOP, Instrument and Test procedure related training.
Review Specification and other relevant documents.
Imparting new implementation for Quality System improvements.
Assist in ensuring adequate stocks of chemical and consumables are maintained
Keep own workplace clean and assist in laboratory housekeeping.
Perform analysis at other facilities of GMP Pharmaceuticals Pty. Limited by following site specific procedures.
Perform any additional responsibility as and when identified by the management.
Ideal Candidate will have
Tertiary qualification or equivalent in Chemical Engineering or related disciplines.
Experiences in QC Lab role within pharmaceuticals is highly regarded.
Demonstrated solid knowledges and experiences in testing, conducting experiments, QC process.
Demonstrated eagerness to learn and improve quality of QC processes and products.
Proven exceptional communication skills in both technical written and professional verbal skills.
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.

The application form will include these questions:
Which of the following statements best describes your right to work in Australia?
Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?
How many years' experience do you have in a quality control (QC) role?
What's your expected annual base salary?
How much notice are you required to give your current employer?