Job Ref #: 2605QC Analysts x2
Industry: Pharmaceutical And Medical/Healthcare
Job Type: Permanent
Positions Available: 2

Job Description

Job Title: Quality Control Analysts X2 – Quality Control Department.

Location: Epping

Employment Type: Permanent

About Us:
We are seeking detail-oriented Quality Control Analysts to join our Quality Control team within an API manufacturing environment. The role supports routine and non-routine laboratory testing activities, ensuring that raw materials, in-process samples, and finished products meet established quality specifications. The Quality Control Analyst performs testing in accordance with GMP, approved analytical methods, and site procedures, while promoting data integrity, safety, and compliance.

Role Purpose:
The Quality Control Analyst supports GMP-compliant laboratory testing to ensure materials and products meet defined quality standards. The role involves performing routine analytical testing, accurately documenting and reviewing results, and working cross-functionally to support manufacturing and batch release activities while maintaining data integrity, safety, and regulatory compliance.

Job Requirements

Key Responsibilities:

• Responsible for the analysis of equipment cleaning samples, raw materials, in-process, and final bulk product samples according to standard operating procedures and test methods
• Chemical and Endotoxin testing of Purified Water
• Assisting the samplers of Purified Water when required
• Carry out analysis and activities in a safe manner in accordance with OHSE and Good Laboratory practice guidelines
• Provide Analytical support to production as and when analysis feedback is required on samples.
• Complete analysis of time as per set target times and dates
• Able to work shifts and weekends on a rotational basis
• Ensure tasks are performed in a manner that is compliant with Good Laboratory Practice and that other Regulatory guidelines are adhered to 

Qualifications & Experience:

• BSc in Chemistry or a National Diploma in Analytical Chemistry or equivalent
• Minimum of 1 years’ experience in a pharmaceutical QC laboratory
• Thorough knowledge and understanding of current Good Manufacturing Practice and the manufacture of Active Pharmaceutical Ingredients
• Must be computer literate in using the MS package as well as LIMS, Veeva Docs, and SAP
• Good practical and theoretical knowledge of analytical chemistry
• Proven problem-solving skills and techniques
• Ability to work independently and as part of a team

Additional Information

• Recognition of Prior Learning (RPL) will be considered

Key Competencies:

• Good organizational skills, with a hands-on and honest approach
• Good interpersonal skills
• Exceptional attention to detail and accuracy
• Good communication (written and verbal) and excellent report-writing skills
• Ability to critically evaluate data and work under pressure
• Ability to perform tasks concurrently even if it means working late or overtime

Why Join Us:

• Be part of a collaborative, safety-focused API manufacturing environment
• Exposure to a wide range of analytical techniques and quality systems
• A collaborative, cross-functional working environment with Production, QA, and Validation teams
• Strong emphasis on training, mentorship, and professional development
• The opportunity to contribute directly to product quality and patient safety
• A culture that values data integrity, safety, and regulatory excellence 

We fully subscribe to the principles of Employment Equity and will make decisions in line with this ethos.

All interested applicants are invited to apply online via www.aspenpharma.com/aspen-jobs/

Closing Date: 15 May 2026

Suitably qualified applicants are invited to submit their CV’s online on or before the specified date. Preference will be given to applicants from designated groups in accordance with laws governing employment equity, where such laws are applicable to the Aspen entity that will employ the successful candidate. If you have not heard from the HR department within 30 days of this advert closing, please consider your application unsuccessful.