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In partnership with our client, a prestigious reference company in the pharmaceutical sector, we are recruiting an Associate Analyst.

responsabilidades chave

Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.
Follow the daily priorities in order to accurately and promptly perform the allocated sample analysis, to meet the requirements of the laboratory plan and area KPIs.
To adhere to the laboratory testing schedule in order to achieve an efficient Quality Control (QC) system.
Take responsibility for all data individually generated and ensure it is in accordance with all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities.
To maintain all checklists, laboratory records and notebooks in which he/she is involved to an acceptable GMP standard and in accordance with company internal procedures.
To maintain good hygiene and housekeeping within the laboratory.
To perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required by the area.
Comply with the high standards in the QC Laboratories.
To bring any discrepancies, deviations or non-conformance in testing or work practice to the attention of QC management in accordance with company internal procedures.
To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories.
Ensure appropriate communication with other internal department in relation to QC work by using the appropriate company processes and their IT platforms.
Undertake any additional tasks to support the laboratory activities as and when required.
Seek out additional information when one feels that the available information is not enough.
Follow all annual performance review requirements, including completion of the self-assessment.
Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice.
Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all company processes and good practice.

competências

- High School diploma (mandatory)
Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (strong preference)
Relevant work experience
Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (preferable)
Experience of GMP practices and HSE standards (preferable)
Technical understanding of GMP practices, analytical theory and techniques
Clear and open communication skills (written and verbal)
Competent (written and verbal) English (preferable for sites where English is not the first language)
Ability and availability to work in shift patterns, as required by business needs
Computer literate with knowledge of the MS Office package
Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.

principais benefícios

- Temporary Worker
- Local - Loures