QC ANALYST BIOPHARMA WATERFORD

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  • Job reference number:15430821
  • Client ID:RI/FRS18842-B
  • Posted on:04-MAR-2019
  • Salary:NEGOTIABLE
  • Location:WATERFORD, WATERFORD
  • Job type:PERMANENT

Benefits: BONUS, CAR PARKING, FLEXITIME, LIFE ASSURANCE, PENSION / PRSA, PERM. HEALTH INSURANCE, RELOCATION PACKAGE, TRAINING / EDUCATION

QC Analyst Biopharm Job
Do you have 2-3 yrs experience of working in a GMP analytical lab then I have a fantastic opportunity for you.

Dungarvan is a thriving seaside market town nestled beneath the Comeragh mountains. The coastline contains some very attractive beaches, Dungarvan itself is served by Waterford ( 30 mins away), Cork (1 hour) and Shannon airports ( 1.5 hours). Journey time to Dublin airport is 2 hours.

Having met with the company again last week I am excited to report that the company is expanding so they have lots of opportunities for progression, ( and fun) along the way.

You will experience a very friendly and calm atmosphere from the moment you walk through the front door.I am delighted to be assisting them with the recruitment of a QC Analyst for their Biopharm Dept this is an excellent opportunity for someone who is looking to really progress their career. The company offer a fantastic salary package together with educational and training assistance , they also appreciate the need for work /life balance too

The company know it is important to hire people who demand high standards of themselves and those around them so if you think you meet the standard and you'd like to be part of their ongoing success, then I'd love to hear from you


Duties:

  • Responsible for developing and validating new tests and procedures
  • Responsible for the completion of specific technological projects and writing up the results of these projects accurately
  • Scientists are permitted to sign all technical documents once their training in this task is successfully completed. This includes laboratory reports, SOPs, protocols, investigation reports and any other documentation issued.
  • Responsible for keeping the laboratory area clean and tidy
  • This person will ensure that all documentation is completed on time, accurately and legibly.
  • They are responsible for their training, keeping their training records up to date and initiating training where possible when free from work.
  • Responsible for updating any relevant documentation as required.
  • Responsible for direct communication with clients in an appropriate manner.
  • To liaise closely with the Section Manager to ensure that resources are available to guarantee that testing activities are completed
  • Responsible for the review of test methods
Requirements:

  • Degree in a Scientific discipline
  • 2-3 years experience in a regulated GMP laboratory environment
  • Experience in biochromatographic techniques (HIC, HILIC, peptide mapping, SEC, reverse phase HPLC), gel techniques (IEF, SDS-PAGE), A280, compendia tests (appearance, pH).& Bioassay experience
  • Able to perform moderately complex and complex laboratory activities including method development, validation and data interpretation.
  • Good team player, organised, accurate, have strong documentation skills

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Please call Felicity on 086 7821714 for a more detailed discussion on the above QC Analyst Biopharma job

This job originally appeared on RecruitIreland.com