Job Description

Who We Are:
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.
Description:
Almac Clinical Services designs and delivers bespoke packaging and logistical solutions for pharmaceutical companies conducting small or large clinical trials for the treatment of a range of diseases and illnesses. We ensure that a supply of clinical material is delivered across the globe to meet the needs of those patients enrolled in a trial, helping to improve patient lives daily.
Overall Role Objectives:
To perform Quality Control (QC) functions within the Material Receiving, Label Control, Distribution and Production areas in order to assure material and products are sampled and released in compliance with agreed specifications and timelines.
Responsibilities:
General Duties:

• To check documentation for completeness and accuracy.
• To Identify any deviations from written procedures and inform Quality Control Supervisor.
• To attend meetings and assist with miscellaneous tasks when required.
• To perform duties under Quality Control personnel supervision.

Quality Control functions within Material Receiving:

• To perform incoming goods sampling and inspection.
• To ensure any customer specific requirements have been carried out by Logistics during booking-in.
• To ensure Almac Clinical Services (ACS) adherence to cGMPs, SOPs and customer instructions through
• performance of job function.
• To assist destruction inspection duties, when required.

Quality Control functions within Label Control and Distribution:

• To inspect Clinical Labels prior to issuance to packaging operations, distribution and direct dispatch from
• ACS.
• To perform verification checks on documentation and clinical material prior to distribution from ACS.
• Quality Control functions within Production:
• To perform regular in-process quality checks on products, processes, room layout and safety to ensure compliance with GMP and ACS procedures.
• To review logbooks and perform facility inspection.

Criteria:

• Academic background in lifescience preferred, minimum diploma holder
• Excellent verbal and written communication skills
• Able to demonstrate logical problem-solving
• Able to work consistently to a high standard under pressure
• Detail-oriented

This is not a lab-based internship; the duration is 6 months. Our office is located in Changi Business Park.
Skills and attributes:

• Quality Assurance
• Quality Compliance