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Open nowPosted 14 days ago

Senior Executive-QC

Piramal Pharma Solutions195 open roles

Where
Piathampur,MP
Work mode
On site
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Your applicationOpen nowSenior Executive-QCPiramal Pharma Solutions · Piathampur,MP

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The clock on this job

Early applications get read.

8.5% of postings close within 7 days. Measured by our own scanner across the market. Piramal Pharma Solutions postings stay open a median of 21 days.

Share of postings closed within
  1. 1.8%1 day
  2. 4.0%3 days
  3. 8.5%7 days
  4. 15.4%14 days
  5. 34.1%30 days
This job: posted 14 days ago

Piramal Pharma Solutions median: 21 days open

The posting

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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

Senior Executive-QC

Job Description

To perform Analytical method validation/method verification/Method transfer activities on different tests like Assay/Dissolution/RS/Residual solvent/Nitrosamine impurities/ dissolution with skill of handling various instruments like LC-MS/HPLC/GC/ UV/IR/AAS/Malven etc and documentation as per Regulatory requirement and maintaining GLP / GMP requirements in lab.

1. Analysis of Finished products, In-process, Hold time, Raw Materials, stability samples and related documentation as per cGMP.

2. Preparation of the Analytical Method transfer/Validation/Verification protocol and reports.

3. Execution of Analytical Method transfer/Validation/Verification activity for new Projects.

4. Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC.

5. Any additional responsibility assigned by section head.

6. Implementation of GLP / GMP requirements.

7. To control and maintain QC Laboratory Records. (Like Laboratory notebook, Chromatograms, and COA etc.).

8. Operations with ENSUR and Track wise. (Carry out OOS, OOT, Lab Investigation report.)

9. Preparation and Standardization of volumetric solutions/ Reagents/ Indicator solution preparation as and when required.

10. Concurrent documentation of analytical records and storage of raw data, online entries in Instrument/ Equipment’s usage logbooks.

11. Analysis of Vendor Approval samples or RLD Samples.

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