QC Analyst

HERO

Job Detail

Location Galway Ireland
Salary Negotiable
Posted
Role Type Permanent
Contact Nela Dobrusova
email Medtech@hero.ie

QC Analyst

Apply Now

Job ID: JOB-13159
QC ANALYST

BASIC SUMMARY:

  • To carry out analytical testing on finished products & raw materials using the correct procedures in order to comply with GMP, Health and Safety, SOP’s and environmental and regulatory requirements while ensuring we meet our customer’s needs.
  • To provide technical support as required by management.

KEY RESPONSIBILITIES:

  • Displays the capability to learn and understand methods showing competency in the following technical areas: HPLC, IR, UV, dissolution & physical testing.
  • Maintain and follow all relevant Standard Operating Procedures (SOP’s).
  • Adherence to the existing methods with reference to pharmacopoeia’s, specifications, regulations and industry standards.
  • Full analysis of raw materials in a timely manner using appropriate analytical techniques with limited analyst related OOS.
  • Full analysis of finished product (tablets, boluses, veterinary drenches etc) in a timely manner using appropriate analytical techniques with limited analyst related OOS.
  • Full analysis of contract manufactured products in accordance with customer specifications with limited analyst related OOS.
  • Incoming inspection of foils, labels, bulk finished goods and injectable.
  • Calibration and maintenance of laboratory equipment as per calibration procedures.
  • To support the laboratory testing schedule in order to achieve an efficient QC system and Customer Service level of >95%.
  • To maintain all laboratory logbooks, notebooks & associated documentation to GLP.
  • Liaise with team leader/supervisor & production so that timely reporting of results is achieved.
  • Ensure timely feedback of all queries as appropriate.
  • To bring to the notice of the team leader/supervisor any discrepancies, deviations or nonconformances in testing or work practice.
  • Display ability and follow up on Corrective Actions.
  • Sending out samples for external analysis when requested.
  • Participating in internal/External Audits.
  • Liaising with external suppliers/vendors in relation to QC consumables.
  • Ensure existing quality procedures are followed and where appropriate suggestions/change control forms are prepared so that the quality system will be continuously improved.
  • To adhere to any agreed internal laboratory rota tasks.
  • To maintain good housekeeping and hygiene within the laboratory.
  • Adherence to laboratory safety measures highlighting areas for improvement.
  • Ensuring that laboratory is kept tidy and that GLP/GMP standards are adhered to.
  • Ensure records pertaining to QC are all kept up to date and filed properly.

COMPETENCIES:

  • Competency in the following technical areas: HPLC, IR, UV, dissolution & physical testing.
  • Ability to build relationships and collaborate with others.
  • Good communication skills, both verbal & written.
  • Maintains the highest standards of ethical behaviour. Escalates issues appropriately.
  • Flexible and shows willingness to learn to develop technical skills.
  • Takes a methodical, systematic and structured approach to organising work.
  • Positive and proactive person who is energised by having great responsibility.

The above is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required and may be subject to change.

QUALIFICATIONS:

  • 3rd level qualification – Bachelor’s degree in a chemistry-based discipline.
  • 0-4 years’ experience in a QC analyst role/ similar role.
  • Strong computer skills in MS Office.
  • Experience working within a pharmaceutical cGLP Environment; with knowledge of EU GMP and US FDA Guidelines.

WORK ENVIRONMENT: (eg. Office, Production)

  • Laboratory

For further information on this role please contact Nela Dobrusova on 0861283369 or medtech@hero.ie 

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/ 

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

 

Nela Dobrusova

JOB-13159

Apply Now

QC Analyst

Nela Dobrusova

Role Type Permanent
Contact Nela Dobrusova
email Medtech@hero.ie
mobile +086 1283369
linkedIn profile click here

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