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Every day, employees working in Takeda’s Global Manufacturing and Supply Chain, and Global Quality business unit are shaping the future of healthcare. They are breaking down barriers and ensuring our life-changing medicines are available, accessible, and affordable to patients. Life-changing for you. Life-changing for patients.

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  • Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.

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QC Analyst - Bray

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Job ID R0033478 Date posted 05/07/2021 Location Wicklow, Ireland

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Job Description

JOB TITLE:                                   QC Analyst

REPORTS TO:                     QC Team Leader

JOB PURPOSE:

The brief requires a thorough knowledge of Good Manufacturing Practice, current FDA & EMEA regulations for solid oral dosage pharmaceuticals for human use and a good working knowledge of manufacturing processes, packaging processes and validation activities used in the pharmaceutical industry. This brief also demands a commitment to the quality effort and the application of good analytical and technical skills

RESPONSIBILITIES:

  • To observe GLP/cGMP at all times
  • Testing of all laboratory samples including Raw Materials, Packaging Components, Product, Validation, Stability, Environmental, OH
  • Performance of laboratory tests as per written procedure or as per pharmacopoeia
  • Recording of analytical results accurately
  • Operation, maintenance and calibration of laboratory instruments
  • Preparation and execution of instrument and method validation protocols
  • To maintain written training records
  • To ensure that the laboratory is kept clean, tidy and safe at all times
  • To report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior
  • Ordering, receiving and controlling laboratory chemicals, reagents and consumables.
  • Receiving and controlling test samples.

GENERAL RESPONSIBILITIES:

  • Drive and promote the corporate values of Takeda-ism within the workplace.
  • Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business. Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
  • Ensure timely completion of all SOP, reading, training and assessment.
  • Other duties as required and directed by the Manager, QC or other Officer appointed by the Board of Directors.

EDUCATIONAL REQUIREMENTS:  

  • BSc. (minimum) in science or a related discipline.

RELEVANT EXPERIENCE

  • Have relevant experience in the pharmaceutical industry.
  • Have a minimum of 2-3 years experience in an analytical lab.

SKILLS/COMPETENCIES

  • Have good organisational, communication, interpersonal and report writing skills.
  • Is adaptable to changing priorities.

Locations

Bray, Ireland

Worker Type

Employee

Worker Sub-Type

Fixed Term (Fixed Term)

Time Type

Full time

Job ID R0033478
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