Sigmar are looking for a Quality Control Analyst for an international pharmaceutical firm well known for its high-quality product.
As a Quality Control you will be responsible for conducting raw material, in process, finished product, and where applicable stability testing according to relevant SOPs and in adherence to the site production schedule and for accurately completing all documentation that supports testing procedures. Your main tasks would be:
- Conduct chemical and physical laboratory tests and analyze raw materials, intermediates and final product to ensure compliance with standards.
- Complete all testing, including special project / protocol testing in a timely manner that supports established production targets and SLAs.
- Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.
- Observe established escalation process for laboratory issues that impact established production-related Service Level Agreements (SLAs) and/or the fulfilment of production goals.
- Author documents that ensure cGMP compliance, such as laboratory investigation, deviations, change controls, change notices, analytical test methods; analytical test method development reports; method validation protocols; method transfer protocols and reports; method verifications protocols and reports; and instrumentation qualification documentation (URS/IQ/OQ/PQ).
- Participate in deviation investigations.
- Seek process innovation and continuous process improvement and perform quality improvement initiatives.
- Support and adhere to established processes and productivity targets.
- Carry out and assist in the ongoing training of new and existing personnel, as appropriate.
- Observe all safety and compliance procedures and actively highlight any safety concerns to help drive the reduction of accidents or near misses.
- The position incumbent is expected to adhere to all cGMP compliance and regulatory mandates and quality requirements and comply with all SOPs.
The next Quality Control Analyst must have a third level qualification in Chemistry or related Science, preferably a Bachelor’s Degree. For that job 2 year ‘experience in the sensitive environment such as pharmaceutical, biotechnology or biopharmaceutical, using HPLC is required. An experience with common laboratory techniques and instruments GC, Dissolution, KF, LOD, Raw material testing experience is preferred.
For that position some soft skills are necessary for the duties’ accomplishment, such as a being a good communicator, energetic and being goal focused.
Are you looking for a new challenge in a worldwide company where career progression and pleasant work environment are met? Don’t wait any longer, send us your CV!
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