Job Description
Arna Pharma Pty Ltd is a leading pharmaceutical company dedicated to improving global healthcare through innovative solutions. With a focus on research, development, and manufacturing of high-quality pharmaceutical products, Arna Pharma aims to address unmet medical needs and enhance patient outcomes worldwide.
With our team of experienced professionals and state-of-the-art facilities, we are committed to delivering excellence in every aspect of our work.
We have two full time positions for highly driven tertiary science qualified Quality Control Analysts with a minimum of two years’ experience in a GMP regulated laboratory to join our team. These positions are based at our facility in Frenchs Forest.
The role, reporting to the QC Manager, will primarily involve performing analyses to ensure chemical composition and properties of materials and product meet specification and quality requirements. Testing will include:
QC testing of raw materials, in-process materials and finished products.
Stability testing of commercial and experimental products.
Characterisation testing for new and existing products.
Other duties will include:
Performing laboratory calibrations and checks to ensure reliability of test data.
Development of test methods for analysis of pharmaceutical starting materials and finished products and method validation work to ensure precision, accuracy and reliability of methods and method performance under differing conditions.
Conducting investigations and testing theories to assess atypical or out of specification results, alternative materials/products, and impact of deviations during testing or manufacture.
Performing and reviewing trending of test data and records.
To be successful in this role, you must be able to demonstrate:
An ability to perform analytical laboratory work in accordance with cGMP.
Excellent attention to detail.
An ability to work within a team and on your own.
Good communication and documentation skills.
Previous experience in testing of pharmaceutical inhalation products (using DU, ACI and/or MSLI equipment) is an advantage but not a prerequisite. Previous experience in the use of HPLC and/or LC-MS is also an advantage but not a prerequisite.
Job Types: Full-time, Permanent
Pay: $73,150.00 – $7+,000.00 per year
Schedule:
Monday to Friday
Application Question(s):
How many years' experience do you have as a QC Analyst?
Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?
Work Authorisation:
Australia (Preferred)
Work Location: In person
With our team of experienced professionals and state-of-the-art facilities, we are committed to delivering excellence in every aspect of our work.
We have two full time positions for highly driven tertiary science qualified Quality Control Analysts with a minimum of two years’ experience in a GMP regulated laboratory to join our team. These positions are based at our facility in Frenchs Forest.
The role, reporting to the QC Manager, will primarily involve performing analyses to ensure chemical composition and properties of materials and product meet specification and quality requirements. Testing will include:
QC testing of raw materials, in-process materials and finished products.
Stability testing of commercial and experimental products.
Characterisation testing for new and existing products.
Other duties will include:
Performing laboratory calibrations and checks to ensure reliability of test data.
Development of test methods for analysis of pharmaceutical starting materials and finished products and method validation work to ensure precision, accuracy and reliability of methods and method performance under differing conditions.
Conducting investigations and testing theories to assess atypical or out of specification results, alternative materials/products, and impact of deviations during testing or manufacture.
Performing and reviewing trending of test data and records.
To be successful in this role, you must be able to demonstrate:
An ability to perform analytical laboratory work in accordance with cGMP.
Excellent attention to detail.
An ability to work within a team and on your own.
Good communication and documentation skills.
Previous experience in testing of pharmaceutical inhalation products (using DU, ACI and/or MSLI equipment) is an advantage but not a prerequisite. Previous experience in the use of HPLC and/or LC-MS is also an advantage but not a prerequisite.
Job Types: Full-time, Permanent
Pay: $73,150.00 – $7+,000.00 per year
Schedule:
Monday to Friday
Application Question(s):
How many years' experience do you have as a QC Analyst?
Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?
Work Authorisation:
Australia (Preferred)
Work Location: In person
💡 Quick Summary
Seeking a career-building opportunity? The QC Analyst |Chemist position is now open for candidates interested in the Manufacturing Jobs sector. This role in Sydney offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Manufacturing Jobs is a plus.
