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QC Analyst 1

  Dublin,  Ireland |  Full time

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Posting Date :  2021-03-09

Job Identification :  10773

Department  :  Quality Control

Reporting to the QC Manager, this fast pace and varied role encompasses laboratory testing across a range of applications along with documenting and reporting of test results in a timely manner. Exceptional attention to detail and a drive for efficiency will be required, with a consistent and accurate approach to testing and documentation whilst adhering to all aspects of company and industry cGMPs. This role is a central part of the QC laboratory operation and supports the wider compliance and quality teams with a common goal for continuous improvement and achieving the company’s business strategy aligned with our Vision, Mission and values.

Key Role requirements: 

  • Conduct raw material, finished product, In-process, stability and water testing in accordance with SOPs and adherence to Good Laboratory Practices principles (GLP) whilst delivering to test schedule assigned.
  • Complete testing and timely documentation write-ups in accordance with Good Documentation Practices (GDP) and delivery to Senior analyst/Designee for review.
  • Notify Senior Analyst/manager and escalate any issues with testing, instrumentation or tasks that could impact on testing timelines. 
  • Notify Senior Analyst/Supervisor of any Out of Specification (OOS), Out of Trend (OOT) as soon as they occur.
  • Author SOPs, protocols, change controls, reports in-line with GDP as required.
  • Maintain Records to GDP in a timely manner, e.g. Lab Notebooks.
  • Ensure workspace is hazard free and maintained in accordance with GLP.
  • Ensure necessary equipment is within calibration and materials are available for testing.
  • Ensure good adherence to test and lab operations scheduling as issued by the Senior Analyst.
  • Champion QC Laboratory initiatives based on continuous improvement and 5S principles.
  • Carry out ancillary QC tasks, e.g. housekeeping, stock checking as required by the QC Manager/Supervisor or designee to ensure the QC laboratory operation runs seamlessly

Other requirements: 

  • Bachelor’s Degree within a Scientific Discipline essential
  • 1 years’ experience in GMP environment within a pharmaceutical (HPLC) environment desired.

Skills/ Knowledge/Behaviours

  • Customer Focus – takes personal responsibility for speed, quality and accuracy of delivery.
  • Self-motivated, determined and able to work under own initiative
  • Progressive – Pro- active approach to best practice within the QC function
  • Collaborative – a team player who can mobilise managers cross functionally to deliver high quality standards
  • Competitive – Self driven with a desire to be the best as an individual and as a business to deliver for our customers
  • Ability to work under pressure in a challenging and fast-moving environment.
  • Excellent oral and written communication skills
  • Excellent Reporting skills
  • Strong interpersonal skills

 

Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve.

About Us

Bimeda is a leading global manufacturer,  marketer and distributor of animal health products and veterinary pharmaceuticals.  Through ongoing expansion and strategic acquisition,  Bimeda has established markets in more than seventy countries worldwide and has R&D,  manufacturing and distribution capabilities across Europe,  North America,  South America,  Africa,  Asia and Australasia.


global

OPERATES
IN OVER
75
countries

people

800+
EMPLOYEES

lab

6
R&D and
REGULATORY
LABS

factory

9
MANUFACTURING
facilities in
7 COUNTRIES

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