QC EM Sampling (Pharma/Biotech) - Part-Time

Responsibilities:

• Execute Environmental Monitoring sampling activities as per the defined location under cGMP.
• Execute compendial method testing such as TOC, Conductivity, Endotoxin, Bioburden when applicable under cGMP
• Track and execute individual training requirements are completed on time to perform sampling under cGMPs and other newly assigned areas of work.
• Follows the priorities for Laboratory equipment documentation, labeling and archiving.
• Ensures sampling delivery is performed in a timely manner.
• Handle data for of SAP entry data and sample dispatching to the required location
• Compiles documents in a complete, accurate and consistent manner to ensure that samples, materials or products and intermediates have been tested, or inspected according to specification and cGMPs.
• Explain, his/her area of work, in health authorities inspections and internal audits
• Other duties assigned by direct supervisor.

About You:

• University Degree in Science related discipline (e.g. chemistry, biology, pharmaceutical sciences, or equivalent experiences)
• Minimum 2 years of experience in a Quality Control Function
• Analytical thinking with problem solving and writing skills
• Motivated and independent
• cGMP/GLP knowledge on QC Lab Equipment and QC testing
• Good communication skills and Strong ability to work cross functional teams
• Ability to work towards timeline