Job Description

The Offer

• Work in a company with a solid track record of performance
• Flexible working options
• Opportunity to make a positive impact

The Job

The role is suited for professionals who are detail-oriented, analytically skilled, and experienced in handling a variety of testing techniques within a cGMP-regulated environment.

Key Responsibilities:

• Conduct in-process testing (e.g. weight, thickness, hardness, disintegration, friability) in accordance with manufacturing batch record instructions.
• Perform routine and advanced testing of raw materials and finished products.
• Operate instruments including Karl Fisher, HPLC, GC, Particle size, and ICP.
• Ensure adherence to data integrity and cGMP documentation practices.
• Lead or assist in investigations and lab documentation processes.
• Collaborate with team members to support timely and compliant laboratory operations.

Work Conditions:

• Must be comfortable working in a regulated lab with PPE (e.g., lab coats, goggles, masks).
• Ability to stand/walk unaided for long periods and lift up to 10 kg.
• Must be open to shift flexibility and occasional weekend work as required.

The Profile

MUST HAVE Qualifications:

• Bachelor’s degree (BS or BA) in Chemistry or a Physical Science discipline.
• Experience in the pharmaceutical industry (strictly no bio-pharma).
• Educational background in Chemistry (BS/BA preferred).
• Working knowledge of Inhalation products (MDI) is a plus (also open to experience with tablets, capsules, liquids, and solids).
• Familiarity with key instruments: Karl Fisher, HPLC, GC, Particle Size Analysis, ICP.
• Strong English proficiency (spoken, written, and reading) for scientific documentation.

The Employer

Our client is a team driven by passion, committed to revolutionizing the way you experience recruitment and HR.

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