Abhishek Pacha

Led Safety Data Sheet (SDS) authoring across EMEA, APAC, LATAM, and the Americas using Lisam ExESS software, ensuring full compliance with global regulatory standards, including OSHA, REACH, and GHS, and inventories including REACH (EU), TSCA (USA), NZIoC (New Zealand), AICS (Australia), and DSL/NDSL (Canada).

· Collaborated closely with the Item Creation Center (ICC) to streamline processes, achieving an average request closing time of 2.1 days

· Utilize basic SQL commands in Salesforce to analyze bulk import, update, and validate large datasets, significantly improving data accuracy and operational efficiency across master data systems.

· Created customized Excel trackers for the team, enhancing request tracking and reporting, which improved workflow transparency and helped monitor progress, leading to faster request closures.

· Independently led and completed five global Merger & Acquisition (M&A) projects, leading product onboarding into Syndigo (PIM) from multiple principals; performed extensive data analysis and cleansing using advanced Excelfunctions to ensure data accuracy, consistency, and compliance with internal standards.

· Maintained close collaboration with Sales, Product Management, and external stakeholdersto align on product data accuracy, completeness, and market readiness, which accelerated the completion of M&A onboarding and directly supported faster go-to-market and business growth.

· Provided key innovation and process improvement inputs that were instrumental in the successful setup of the Master Data Management (MDM) and Item Creation Center (ICC), helping establish scalable, efficient workflows and global data governance practices.

Developed compliant Safety Data Sheets and labels detailing hazards, handling, and safety information for global chemical regulations.

Validated regulatory documents against GHS classification, CLP regulations, and REACh compliance requirements.

Collected data and conducted risk assessments to support SHEQ initiatives and sustainability efforts.

Leveraged Akeneo PIM for streamlined product management across multiple categories.

Produced weekly reports on compliance status to inform stakeholders of regulatory updates.

Controlled engineering activities for upstream processing of biosimilars, ensuring compliance with quality assurance and timelines.

Trained on multiple bioreactor systems, including Sartorius (10 L to 2500 L), ABEC, and PALL single-use bioreactors.

Managed dispensing of raw materials to shop floor while overseeing centrifuge operations (Alfa Laval, GE Westfalia).

Utilized Distributed Control System (DCS), Laboratory Information Management System (LIMS) by Labware, and Systems Applications and Products (SAP) ERP software for effective inventory management and process control.

Participated in audits and implemented corrective actions to address findings, including INVIMA, Egypt, Belarus, State FDA, and internal QA assessments.

Performed Factory Acceptance Test for autoclave equipment at pharmaceutical lab in Gujarat.

Developed and validated Electronic Batch Manufacturing Records using Werum PAS-X software.

• Ensured high standards for sourced final products through rigorous inspections and testing.
• Conducted thorough inspections of oil products to verify compliance with established standards.
• Monitored oil machinery and production processes to maintain operational effectiveness.