Mohammad Tajammul Furquan

Bioprocess| Bio-similars| Small peptides| Cell line development| Fermentation process

Role: Deputy General Manager at Vimta Labs Ltd
Location: Hyderabad, TG, IN
LinkedIn followers: 500 followers

General Business & ManagementView LinkedIn profile

About Mohammad Tajammul Furquan

Passionate and driven Biotech professional with extensive industrial experience in…

Experience

Deputy General Manager
Vimta Labs Ltd
Sep 2025 — Present · Hyderabad, IN
Lead Microbial USP and Cell Line Development

Skills

Gmp
Molecular Biology
Western Blotting
Good Laboratory Practice (Glp)
Chromatography
Lifesciences
Purification
Protein Expression
Sds-Page
Electrophoresis
Sop
Technology Transfer
Bioinformatics
Downstream Processing
Assay Development
Life Sciences
Physiology
Microbiology
Biofuels
Glp
Genomics
Biotechnology
Protein Purification
Polymerase Chain Reaction (Pcr)
Hplc
Biopharmaceuticals
Elisa
Gel Electrophoresis
Protein Chemistry
Vaccines
Yeast Systems
Genetics
Dna
Pcr
Biochemistry

Contact information

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Work email
•••••@vimta.com
Personal email
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Current company

Vimta Labs Ltd

Research Services · 1.8K employees · Founded 1984 · Hyderabad, India

Founded in 1984 with headquarters in Hyderabad, India, VIMTA LABS LTD. is a leading contract research and testing organization, providing bio/pharmaceutical companies an integrated scientific, technical, and regulatory expertise to support all stages of drug development and manufacturing process. Our service portfolio includes preclinical and clinical research; and cGMP laboratory services viz, method development, microbiology, stability testing, extractables & leachables, process validation, quality control, physical characterization etc. In our 40 years of journey, we have gained in-depth scientific and technical expertise through working with a variety of molecules and formulations in different therapeutic areas. We support the needs of more than 300 bio/pharmaceutical companies across the globe, from virtual to large pharma and biopharma, through a wide range of expertise. Our team of 1300+ professionals constantly endeavors to provide timely scientific solutions and services to help customers manage their drug development and manufacturing processes more efficiently without compromising quality. We have a track record of strict compliance with regulatory requirements (cGMP, GLP, GCP) and Standards (ISO 17025, ISO 15189, ISO 9001), and have undergone over 40 regulatory audits successfully from regulatory agencies across the globe, including DCGI, NGCMA, USFDA, WHO, MHRA, ANSM, ANVISA, BfArM and DRAs of Denmark, Sweden, Portugal, and Ukraine.

vimta.com

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About Mohammad Tajammul Furquan

Experience

Deputy General Manager

Skills

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