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QC Associate Senior
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QC Associate Senior

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1 Vacancy
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Jobs by Experience

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3-5years

Job Location

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Dublin - Ireland

Monthly Salary

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Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2080582

Job Title: QC Associate (Senior) Recruiter- Jessica Amaral


Duration of Job: 12 months Salary- 30-31Euros per hour


Join us! There has never been a better time to do your lifes best work!


The Role:

Our client, a multinational bio pharmaceutical company, is seeking a QC Associate (Senior) to join its expanding team in its Dun Laoghaire site, which includes a bio processing suite and laboratories.

This role will be responsible for leading, coordinating, facilitating, and undertaking activities pertaining to lab operations and compliance, with minimal supervision, acting as a role model for other lab colleagues. The role undertakes implementing continuous improvement projects and supporting a lean culture and Right First Time (RFT). The role also represents the QC unit by liaising with internal and external customers.



Job Duties:
  • Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
  • Participate in the peer review of analytical data.
  • Responsible for providing technical guidance and applying expertise and critical thinking to help to resolve technical issues.
  • Lead training of staff on technical aspects of job as required.
  • Develop, revise and implement procedures that comply with appropriate regulatory requirements.
  • Qualification of analytical equipment and related testing functions.
  • Participate in Analytical Method Transfers
  • Compliance with Standard Operating Procedures and Registered specifications.
  • Ensure the laboratory is operated in a safe manner
  • Maintain quality systems within the QC laboratories to ensure ongoing compliance to cGLP and cGMP.
  • Ensure timely completion of Laboratory Investigation Reports and deviations through the Non-Conformance procedures.
  • Participate in the generation and update of SOP s, trend data, investigations, non-conformances, validation protocols, reports, method validation/verifications and equipment qualifications.
  • Participate in regulatory agency inspections as required.
  • Plan and implement procedures and systems to maximise operating efficiency.
  • Manage and contribute to the achievements of department productivity and quality goals.


Requirements

  • Bachelor s degree in a Science related field is required.
  • Experience in a wide variety of analytical techniques including but not limited to cell based- Bioassays, Immunoassays, Cell Culture (use of cells to execute bioassays) and Aseptic Technique. Experience with liquid-handling robots is also preferable.
  • 5+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry,
  • Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
  • Working knowledge of aseptic compliance within the manufacturing environment and demonstrated leadership and communication skills to communicate requirements to colleagues
  • Auditing documentation and operation process
  • Demonstrated ability to interact with regulatory agencies


Benefits


  • Benefit from Independent Solution s ethical principles.
  • Pre-interview preparation before attending the interview and help to use STAR technology to answer the questions.
  • While placed on client sites you will be an integral part of our team, gaining support and access to the knowledge and experience of our cross-functional Life Science team.
  • We offer attractive rates - competitive margins compared to our competitors.
  • Payment on time and in full.
  • We are recognized as approved suppliers to leading key pharmaceutical and medical device companies.



You must have the right to work in Ireland for this role.

If you have the above skills & experience, please contact or apply at

Independent solutions provide End to End solutions to the life sciences and we are expertise in Bio-Tech, Biopharma, and medical sectors. We are the sole source of exceptional Project managers, Engineering.



Bachelor s degree in a Science related field is required. Experience in a wide variety of analytical techniques including but not limited to cell based- Bioassays, Immunoassays, Cell Culture (use of cells to execute bioassays) and Aseptic Technique. Experience with liquid-handling robots is also preferable. 5+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Working knowledge of aseptic compliance within the manufacturing environment and demonstrated leadership and communication skills to communicate requirements to colleagues Auditing documentation and operation process Demonstrated ability to interact with regulatory agencies

Employment Type

Full Time

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