Mughda Khaladkar Email & Phone Number | • 6+ years of experience as Validation Specialist and QA Specialist in cGMP regulated pharmaceutical organization. • Extensive experience with developing standard operating procedures, specifications, and protocols, change controls, and impact assessments. • Detail oriented with strong business, planning, validation, implementation skills in the design, development, testing, validation, deployment, and support in the Software development lifecycle of a project-with a strong focus on the manufacturing and production of planning applications, Change Control Management testing, and GMP procedures. Exceptional communication and interpersonal skills. • Extremely knowledgeable with the Software Development Life Cycle, Data Integrity, GMP Assessments, Risk Assessments, Audit Trails, Validation Plans, IQ/OQ/PQ/RTM, validation reports, SOP's, GAMP 5, 21 CFR Part 11, risk analysis, testing and implementation of a project.

Mughda Khaladkar

• 6+ years of experience as Validation Specialist and QA Specialist in cGMP regulated pharmaceutical...
Arden, North Carolina, United States

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Mughda Khaladkar’s Phone Numbers +1 800-711-****

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Mughda Khaladkar’s Location Arden, North Carolina, United States

Mughda Khaladkar’s Current Industry Thermo Fisher Scientific

Mughda Khaladkar’s Prior Industry Hikama Pharmaceticals | Allergan | Wyeth Biopharma

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QA Specialist

2019-02-01 00:00:00 - Present

QA Specialist

2018-01-01 00:00:00 - 2019-01-01 00:00:00

Validation Analyst

2016-06-01 00:00:00 - 2017-12-01 00:00:00

Validation Engineer

2015-08-01 00:00:00 - 2016-05-01 00:00:00

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Mughda Khaladkar is a • 6+ years of experience as Validation Specialist and QA Specialist in cGMP regulated pharmaceutical organization. • Extensive experience with developing standard operating procedures, specifications, and protocols, change controls, and impact assessments. • Detail oriented with strong business, planning, validation, implementation skills in the design, development, testing, validation, deployment, and support in the Software development lifecycle of a project-with a strong focus on the manufacturing and production of planning applications, Change Control Management testing, and GMP procedures. Exceptional communication and interpersonal skills. • Extremely knowledgeable with the Software Development Life Cycle, Data Integrity, GMP Assessments, Risk Assessments, Audit Trails, Validation Plans, IQ/OQ/PQ/RTM, validation reports, SOP's, GAMP 5, 21 CFR Part 11, risk analysis, testing and implementation of a project.