Ansa Paul

Qc Operation Analyst Sample Manager @Terumo Pharmaceutical Solutions Division

Wuppertal, DE
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Oct 2025 — Present

Qc Operation Analyst Sample Manager @Terumo Pharmaceutical Solutions Division

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Wuppertal, DE

Sample and reference standard management as well as the management of stability studiesCoordination with the customer and the outsourced laboratory for sample acceptance and dispatch-Responsible for laboratory systems such as LIMS and procurement for QC in SAP-SOP review and the MasterControl approval process-Procurement of equipment, materials, and reagents to meet the lab\'s needs-actively participate in operational improvement initiatives to Improve process efficiency-Participate in Self inspections, Customer audits and Authority Inspections.

EDUCATION

2010 — 2012

G.H.S.S Manjapra

Higher Secondary School, Biology

2017 — 2018

Volks Hochschule Bremen

B1 Level German

2012 — 2015

Christ University, Bangalore

Bachelor’s Degree

2015 — 2017

Jacobs University Bremen

Master’s Degree

2004 — 2010

St.Joseph High School Kidangoor

High School

SKILLS

Microsoft WordMicrosoft ExcelPowerpointComputational BiologyTeamworkScienceBiotechnologyEnglishPythonLatexChemistryResearchMathematicaMicrobiologyBiologyMicrosoft OfficeMicrosoft PowerpointSocial MediaBioinformaticsZoology

ABOUT ANSA PAUL

As a QC Operation Analyst at Terumo Pharmaceutical Solutions with over 4 years of experience, I contribute to sample and reference standard management, stability studies, and laboratory system oversight, including LIMS and SAP. My responsibilities also encompass the procurement of equipment and materials, SOP review, MasterControl approvals, and ensuring compliance during inspections and audits. With more than 3 years of prior experience at WuXi Biologics, I have honed my skills in sample management, stability studies, and operational improvements within GMP-compliant environments. My expertise lies in enhancing processes, coordinating with internal and external stakeholders, and maintaining precision in quality operations to consistently meet organizational and regulatory standards in the biotech and pharmaceutical industries.

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