Quality Control Analyst - cGMP & Data Integrity

Piramal Pharma Limited

United Kingdom

On-site

GBP 38,000 - 52,000

Full time

10 days ago
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Job summary

Piramal Pharma Solutions in the United Kingdom is seeking an Executive - Quality Control to perform analyses of AMV/AMT, finished product, stability samples and raw materials in compliance with cGMP and USFDA. The role requires hands-on experience with HPLC, GC, FTIR, dissolution, KF, LC-MS/MS and other instruments, plus documentation, data integrity and adherence to GDP and ALCOA++.

You will support QC activities, record maintenance, and deviations reporting, contributing to site quality and

Qualifications

  • Analyst who is able to performed analysis of AMV/AMT, finished product, stability samples and raw materials as per cGMP and USFDA requirement.
  • Able to prepare protocol and report and other related documentation as per GDP.
  • Should have hands‑on experience on HPLC, GC, FTIR, Dissolution Test apparatus, KF, LC-MS/MS, AAS, Malvern PSD analyser etc.
  • Should have sound knowledge of cGMP, GLP, GDP, ICH and ALCOA++.

Responsibilities

  • Analyst who is able to performed analysis of AMV/AMT, finished product, stability samples and raw materials as per cGMP and USFDA requirement.
  • Able to prepare protocol and report and other related documentation as per GDP.
  • Should have hands‑on experience on HPLC, GC, FTIR, Dissolution Test apparatus, KF, LC-MS/MS, AAS, Malvern PSD analyser etc.
  • Should have sound knowledge of cGMP, GLP, GDP, ICH and ALCOA++.

Skills

HPLC
GC
FTIR
Dissolution Test apparatus
KF
LC-MS/MS
AAS
Malvern PSD analyser

Job description

Piramal Pharma Solutions in the United Kingdom is seeking an Executive - Quality Control to perform analyses of AMV/AMT, finished product, stability samples and raw materials in compliance with cGMP and USFDA. The role requires hands-on experience with HPLC, GC, FTIR, dissolution, KF, LC-MS/MS and other instruments, plus documentation, data integrity and adherence to GDP and ALCOA++.

You will support QC activities, record maintenance, and deviations reporting, contributing to site quality and

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