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Wasim mohammed

@wasimmohammed

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Production professional at OneSource Specialty Pharma overseeing injectable manufacturing and cGMP compliance.

India

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What I'm looking for

I’m seeking to use my experience in operations, quality assurance, and continuous improvement to contribute to an innovative organization.

At OneSource Specialty Pharma, I oversee production operations for injectable dosage forms, including vials, pre-filled syringes, and cartridges. I manage deviations and investigations, implement CAPA, and support regulatory and customer audits.

At Stelis Biopharma, I managed manufacturing activities across engineering, commercial, and process validation batches, and participated in media fill activities. I also analyzed process data to support operational improvements.

At Cipla, I managed API production under cGMP and QMS guidelines and supported USFDA, TGA, and MHRA audits. My experience also includes soft gelatin capsule production at Geltec and manufacturing operations at Biocon.

Experience

Work history, roles, and key accomplishments

Current

Senior Executive – Production (Injectables)

Current

OneSource Specialty Pharma

Jan 2026 - Present (8 months)

Oversee production operations for injectable dosage forms including vials, pre-filled syringes, and cartridges. Ensure compliance with cGMP, QMS, and regulatory requirements across all manufacturing activities.

GMP QMS CAPA Regulatory Compliance Production Planning Injectables Vials Pre Filled Syringes Cartridge Audit Readiness Continuous Improvement

Senior Executive

Maiva Pharma

Oct 2024 - Jan 2026 (1 year 3 months)

Ensure QMS compliance with regulatory standards. Manage deviations and implement corrective actions, and support internal and external audits.

QMS CAPA Regulatory Compliance Audit Process Improvement

Senior Associate

Stelis Biopharma

Feb 2022 - Oct 2024 (2 years 8 months)

In charge of manufacturing activities, ensuring smooth operations and compliance with regulatory guidelines. Managed end-to-end manufacturing processes, including batch execution, troubleshooting, and process improvements.

Manufacturing Batch Processing Troubleshooting Process Validation Media Fill Data Analysis Manpower Planning GMP QMS

Senior Executive

Cipla

Apr 2018 - Feb 2022 (3 years 10 months)

Managed API production under cGMP and QMS guidelines. Successfully faced multiple regulatory audits, including USFDA, TGA, and MHRA, ensuring strict adherence to compliance requirements.

API Production GMP QMS Regulatory Audits FDA TGA MHRA CAPA Deviation Management Materials Management Workforce Scheduling Production Reporting

Executive

Geltec

Jul 2016 - Mar 2018 (1 year 8 months)

Supervised soft gelatin capsule production while ensuring GMP compliance. Managed manpower and material planning to ensure seamless production flow.

Gelatin Capsules GMP Manpower Planning Material Planning BMR Documentation Production Efficiency

Junior Executive

Biocon

Jan 2015 - Jan 2016 (1 year)

Worked on the shop floor, handling chemical reactions and process operations. Ensured adherence to GMP and QMS protocols while executing manufacturing procedures.

Chemical Reactions Process Operations GMP QMS Manufacturing