In Process Quality Assurance Specialist- Shifts Days/Evenings
This position requires an In Process Quality Assurance Specialist with experience in the Pharmaceutical industry to ensure batches are manufactured in compliance with regulatory requirements, company policy and procedures.
The key responsibilities include:
* Supporting batch manufacture by reviewing batch records, performing in-process checks, and sampling for quality assurance.
* Overseeing batch release on the floor to ensure compliance with GMP regulations.
* Reviewing documentation such as batch records, logbooks, and standard operating procedures for accuracy and completeness.
* Participating in investigations related to manufacturing and preparing reports and forms as required.
* Performing process audits and monitoring GMP compliance during production activities.
* Managing retain samples and supporting training activities.
Requirements:
* Minimum 3 years of QA experience in a Pharmaceutical GMP environment.
* Deep knowledge of quality assurance terminology and methods.
* Professional certification, such as Six Sigma or CQA.
* Experience working with HPRA and FDA accredited facilities.
Benefits:
* Healthcare for Employee & Family
* 33% Shift Allowance
* Bonus
* Pension 5%-5% contribution by Employer
* 23 days holidays
* Flextime