QC Analyst (Sampling)

Singapore   |   full time   |   Job ID: 9221 

As QC Specialist (Sampling), you are responsible for performing laboratory specific activities, such as sampling, sample administration and simple analytical testing, laboratory supplies inventory control. Please note that this position is a contract role and is subject to renewal.

Your responsibilities are:

• Clean Room and Clean Utility sampling and testing as per EM program.
• Incoming raw material sampling and identification testing as per sampling plan and testing plan.
• Sample management for all QC laboratories including receiving, labelling and safely storing samples to be tested. Arrange sample shipment to external testing laboratories.
• GMP-compliant and on time completion documentation of sample administration and analyses and the associated activities as required by method SOPs, control regulations, QC planning documentation, and pharmacopoeia. 
• Enters analysis results into the SAP/LIMS system, stores and archives source data and ensures data integrity for the assigned work, permanently monitors assigned analysis methods, including trend controls of data. 
• Maintains and calibrates analysis equipment with associated documentation, assists qualifications of analytical equipment with associated documentation and schedule control. 
• Promptly informs the laboratory manager about nonconforming analysis values or exceeded limit values, and initiates and processes non-conformance reports (non-conformances and OOx) 
• Assists with preparing reports and with drafting and revising test procedures and SOP’s. 
• Assists and trains new employees/trainees 
• Performs all assigned activities while observing all internal and regulatory requirements (safety and quality)

What you have to offer:

• Diploma or equivalent with experience in the pharmaceutical sector, or vocational training as biology/microbiology/chemistry laboratory associates, or comparable qualification with multiyear professional experience in a quality control function sciences  
• 2 to 5 years of industry experience in an analytical, cGMP-regulated environment
• Fluent written and verbal English 
• High degree of conscientiousness and diligence (documentation, order and cleanliness at the workstation) 
• Constructive, solution-oriented work habits, flexibility
• Self-starter and pronounced willingness to learn 

Your Benefits:

BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.

Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.

How to apply:

Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.

Please note:

Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.

We are looking forward receiving your application.