Piramal Pharma Ltd Pithampur - Walk-in 28th August 2021 for QC Executive, QC Manager

Company Name:Piramal Pharma Limited

Position Name: QC Executive,QC Manager

Qualification: UG -B.Pharma in Any Specialization

Experience: 3 to 13 year(s) of Experience

Location: Indore, Pithampur

Job Description: We have Hiring For QC Executive,QC Manager in Piramal Pharma Limited !

Time and Venue

Walkin Interview on 28th August from 11.00 AM – 2.00 PM onwards

Piramal Enterprises Limited Plot # 67-70, Sector 2, District: Dhar, Pithampur, Madhya Pradesh 454 775 India

Walk-In Interview QC Executive : role and responsibilities

Ensure testing & release of Raw Materials, Finished products and Packaging Materials as per cGMP in time.
Testing and release of Raw Materials, Finished products and Packaging Materials as per cGMP requirement.
Ensure analysis of stability samples and related documentation as per cGMP requirement.
Facing Internal audits and External Audits and ensure compliance.
Review and approve all QC document like SOPs, STPs, GTPs etc.
Control of operating expenses.
Ensure effective implementation of systems and procedures as per GMP, GLP, ISO 9001, ISO 14001 and other regulatory requirements.
Carry out OOS / OOT / incident Investigation.
Managing of control samples.
To review Pharmacopeia i.e.USP, BP, IP, EP and ensure that the changes proposed are implemented and relevant PHL documents are being updated before the effective date.
Ensure Data entry and approval in system.
Set annual performance goals for Team, monitors performance and guide them to attain it.
On job training as necessary to develop skills and improve productivity.
Ensure the training to new persons as per procedure.
Review of laboratory data.
To ensure calibration & maintenance of laboratory equipment.
Review of work output and pending work.
Responsible to verify and checking of audit trail functioning of all QC instruments like HPLC, GC, UV and FTIR instrument.

Walk-In Interview QC Manager : Role and responsibilities

Preparation and revision of specification and standard test procedure of RM / FG.
Preparation and revision of all SOP, GTP and other QC documents.
Monitor and implementation of all pharmacopeia changes as per IP/BP/USP/EP/JP.
Qualification of new instruments.
Related documentation like SOPs, STPs, GTPs etc.
Preparation of investigation report like Event, OOT, OOS and Incident.
Change the documents through change control.
Reviewed and Released of Raw Materials and related documentation as per cGMP requirement.
Calibration & maintenance of Instrument.
Review of laboratory data and calibration data
Co-ordinate for AMC for equipment and keep record of maintenance of equipment.
Preparation of secondary reference standard as per standards and related documentation.

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