---
title: "Anuradha K. - Production Supervisor in Pimpri Chinchwad | Tal"
description: "Meet Anuradha K., MBA (Pharma Management) | 2.8 yrs in GMP-driven Manufacturing | Transitioning into Product, Market & Strategy Roles based in Pimpri Chinchwad."
image: "https://tal.club/meet/anuradha-4/share-image"
---

# Anuradha K\. on Tal

## Headline

MBA \(Pharma Management\) \| 2\.8 yrs in GMP\-driven Manufacturing \| Transitioning into Product, Market & Strategy Roles

## About

I’m an MBA candidate specializing in Pharmaceutical Management with 2\.8 years of experience across solid, liquid, and semi\-solid dosage manufacturing in GMP\-regulated environments\. My professional journey began on the manufacturing floor — managing process validation, quality compliance, and technology transfer across tablets, MDIs, eardrops, and creams\. Over time, this experience shaped my understanding of how innovation, compliance, and business strategy intersect in the healthcare ecosystem\. Currently, through my MBA and courses in Drug Commercialization \(University of San Diego\) and Intellectual Property in Healthcare \(University of Pennsylvania\), I’m expanding my skillset in product strategy, market analysis, and healthcare operations\. My goal is to transition into roles such as Product Manager, Healthcare Analyst, Regulatory Affairs Associate, or Strategy Analyst, where I can apply both my technical foundation and business insight to drive growth, compliance, and innovation\. Key Strengths: GMP Compliance \| Regulatory Documentation \| Product Lifecycle \| Process Optimization \| Market Research \| Cross\-functional Collaboration

## Location

Pimpri Chinchwad

## Work experience

Production Supervisor at NuLife Pharmaceuticals, Nov 2022 \- Present · 3 yrs 8 mos, Bhosari, Production Officer – Creams & Ointments Department NuLife Pharmaceuticals \| Apr 2025 – Present \-Overseeing semi\-solid dosage production with focus on quality consistency and GMP standards\. \-Collaborating with F&D and QA for formulation scale\-ups and process optimization\. \-Ensuring regulatory documentation accuracy and maintaining audit readiness\. Metered Dose Inhaler \(MDI\) & Eardrops Department NuLife Pharmaceuticals \| Apr 2023 – Mar 2025 \-Managed sterile liquid dosage manufacturing including formulation and aseptic filling\. \-Monitored environmental controls ensuring compliance with FDA and WHO\-GMP guidelines\. \-Collaborated with QA for batch release, deviation control, and documentation verification\. Production Trainee – Tablet & Capsule Department NuLife Pharmaceuticals \| Jan 2023 – Mar 2023 \-Operated and monitored key tablet manufacturing equipment and maintained BMRs\. \-Supported process validation and documentation for compliance and audit readiness\.

## Education

Master of Business Administration \- MBA, Pharmaceutical Marketing and Management, Manipal Academy of Higher Education

Bachelor of Pharmacy \- BPharm, Pharmacy, Shri Chankya Education Societys Indira College of Pharmacy, Tathawade, Pune 33

[View the original profile](https://tal.club/meet/anuradha-4)

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