This is a sample alert
Our client, is looking to engage with an Analytical consultant to support their team.
Key responsibilities include:
1. Adherence to cGMP (Current Good Manufacturing Practice) and Good Laboratory Practice.
2. Production process control in coordination with production for receipt of Inprocess samples.
3. In process, finished product and stability samples inspection, testing and review of Audit trails for Inprocess analysis.
4. Identification recording and evaluation of all Nonconforming products. Corrective and preventive actions as and where applicable. Preparation, Review and maintenance of Quality Records and Review of product specifications and Analytical reports.
5. Issue and review of log sheets/Annexures/Raw data books/Checklist/log sheets for record times.
6. Handling and Investigation of OOS, OOT, Deviations and Incidents and ensuring effective implementation of EHS management system in the organization.
7. Coordinating with the cross functional teams to address regulatory queries. Maintaining team co-ordination and communicate relevant EHS issues to concerned personnel.
This is a 6 months project full time onsite in Malaysia.
Work Experience in Analytical OOS, OOT
Experience in working and implementation of EHS management
High proficiency in Microsoft Office
Excellent Communication and interpersonal skills required
An Indian biopharmaceutical company manufacturing generic active pharmaceutical ingredients that are sold in over 120 countries across the globe
Pharmaceuticals
12+ years
1
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