Executive - Quality Control

Piramal Pharma Ltd; Barneveld; On-site; EUR 32,000 - 52,000; Full time

Job summary

Piramal Pharma Solutions is seeking an Executive - Quality Control to support GMP-compliant testing, sampling, and documentation in Barneveld, Gelderland, Netherlands. The role is focused on routine QC activities within a CDMO environment.

The position involves inward and area cleaning, sampling of packaging materials, performing USP analyses, COA preparation, and meticulous filing of reports under supervision to ensure regulatory compliance.

Responsibilities

• P.M. Inward and area cleaning.
• Sampling & Analysis of packaging material for routine as well as new project samples.
• Machine trial sample & market complaint sample analysis.
• Perform the All USP Analysis & COA Preparation
• Documentation as per GMP & Regulatory requirement.
• Arrangement of Art work, product file, Spec, STP, SOP & other related documents
• Filing of Reports in respective area.
• Completion of all assign work by Manager/ HOD.

Job description

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Executive - Quality Control

Job Description

• P.M. Inward and area cleaning.


• Sampling & Analysis of packaging material for routine as well as new project samples.


• Machine trial sample & market complaint sample analysis.


• Perform the All USP Analysis & COA Preparation


• Documentation as per GMP & Regulatory requirement.


• Arrangement of Art work, product file, Spec, STP, SOP & other related documents


• Filing of Reports in respective area.


• Completion of all assign work by Manager/ HOD.