Sreeparna Lahiri

Director Qa

Sreeparna Lahiri is a highly qualified expert, who works in Eidos Therapeutics main office of which is in 1096. on the position of Director Qa from 2019. This person has earned professional experience in more than 13 positions at different companies. Sreeparna Lahiri went to the The Johns Hopkins University and received education there from 2011 to 2014. San Francisco, California is the city, where this professional was lastly known to live. This expert's phone number and email are easily accessed through this website on demand.
Name variants:
Sreeparna Lahiri

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Contact Information

Last Update
Jul 13, 2022
Email
sl**@eidostx.com, sr**@gmail.com, sl**@genitope.com
Location
San Francisco, CA
Company
Eidos Therapeutics

Workplace

Director Qa

Work History

Director Qa

101 Montgomery St, San Francisco, CA 94129
from Mar 2019

Associate Director Qa

San Diego, CA
Mar 2018 — Mar 2019

Qa Consultant

469 west Huron St, Chicago, IL 60654
Oct 2017 — Mar 2018

Qa Consulting

4200 Bohannon Dr SUITE 250, Menlo Park, CA 94025
Supporting Parenterals Drug Product (DP) validation/PPQ efforts
Sep 2017 — Sep 2017

Senior Quality Manager

Jan 2016 — Aug 2017

Qa Manager

249 east Grand Ave, South San Francisco, CA 94080
Leadership role as a QA representative in critical projects, CMC, and chair Material Review Board (MRB) meetings QA oversight of API and solid oral dosage drug product (DP) manufacturing C...
Mar 2013 — Dec 2015

Senior Quality Specialist

Illinois
Managed projects and product release in DP and Labeling and Packaging Approved label text and label proof for clinical drugs QA oversight of CMOs and partners QA representative in CMC me...
Aug 2008 — Apr 2011

Senior Qa Technical Associate

Managed and improved quality systems Led setting up of quality management software (QMS) Audited technical data and reports Trained employees
Jun 2006 — May 2008

Qa Associate Iii

Quality systems;CAPA, deviation, change control Batch record review OOS investigations.
2005 — 2006

Qa Associate

New Brunswick, NJ
Planned and released commercial and clinical lots Used databases for lot release; ERP, access Reviewed and approved manufacturing batch records; APIs, and finished product. QC data revie...
Mar 2004 — Jun 2005

Qc Associate

Managed stability programs, chambers, and wrote stability reports for IND submissions. Inspected raw materials. Identified quality issues and presented data in Material Review Board meetin...
2000 — 2003

Lecturer and Clinical Biochemistry Lab Assistant

Lecturer and clinical biochemistry laboratory assistant at JSS Medical College/Hospital, Mysore, India
1997 — 1999

Senior Qa Technical Associate

Education

Occupations

Executive
Director
Deputy Director
Scientist
Biotechnology Professional
Operations Manager
Deputy Manager
Chief Executive
Biologist
Biological Scientist

Skills

Gmp
Fda
Capa
Biotechnology
Quality System
Validation
Regulatory Affairs
Change Control
Quality Assurance
Biopharmaceuticals
Hplc
Pharmaceutical Industry
Glp
21 Cfr Part 11
Clinical Development
U.s. Food and Drug Administration
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