DHAR · FULLTIME
Deputy Manager-QC

Piramal Pharma Solutions
Dhar · onsite · Posted 13d ago
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Section · 01
About this role
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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
Deputy Manager-QC
Job Description
Analysis of Finish product and stability samples.
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
Deputy Manager-QC
Job Description
Analysis of Finish product and stability samples.
- Analysis of Finished products, Raw Materials, stability and related documentation as per cGMP.
- Receipt/Inward/Storage of QC samples and Disposition of sample after analysis.
- Preparation and Standardization of volumetric solutions/ Reagents/ Indicator solution preparation as and when required.
- Concurrent documentation of analytical records and storage of raw data, Online entries in Instrument/ Equipments usage log books.
- Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC.
- Requirement / Procurement of chemical/ reagents/ standards/ columns required for new project.
- Any additional responsibility assigned by section head.
- Maintenance of Bin Card of chemical store.
- Implementation of GLP / GMP requirements.
- To control and maintain QC Laboratory Records. (Like Laboratory note Book, Chromatograms, and COA etc.).
- Analysis of Vendor Approval samples.
- Review of laboratory chemicals.
- Responsible for only run the method in the HPLC does not access to Change the method, report format, cancellation of any run, or system and method configuration.
- Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site.
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Section · 02
Skills
CGMPGLPHPLCDocumentation
Section · Company
About Piramal Pharma

Piramal Pharma Solutions
Pharma
4.6k+
employees
2020
6 years old
Mumbai, Maharashtra
US
₹6L PA avg
Avg at Piramal Pharma
About
Piramal Pharma Solutions strives to enhance value for the patients by reducing the burden of disease through early-stage drug discovery and clinical development services.
Industries
PharmaBiotech & Life sciences
Employee ratings
10 reviews
4.0/ 5
Culture
3.1
Career growth
2.9
Work-life
3.1
Employees rate it well for
Overall Company40Job Security39
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