Laboratory Scientist | Molecular Diagnostics & Genomics | GxP / GMP Certified | Automation & High-Throughput Operations | Precision Medicine MSc
Aktualisiert am 17.06.2026
Profil
Freiberufler / Selbstständiger
Remote-Arbeit
Verfügbar ab: 21.06.2026
Verfügbar zu: 100%
davon vor Ort: 100%
Laboratory Automation ? Hamilton Robotic Systems
Nucleic Acid Technologies ? NGS & Molecular Diagnostics
PCR / qPCR ? primer design
GxP / GMP Compliance & Audit Readiness
Gel electrophoresis & gel imaging
Reverse transcription & cDNA library preparation
PBMC isolation & blood fractionation
Bacterial & pathogenic microbial cultures
Mammalian cell culture principles (CHO
HEK293)
Autoclave sterilisation & S1 biosafety lab operations
Cold chain & cryogenic sample management (?80°C)
Culture media preparation
Spectrophotometry / photometric analysis
Transcriptome assembly & QC
Contaminant removal & error correction
Density gradient & differential centrifugation
HPLC (principles)
ELISA (principles)
Protein analytics & purification ? ÄKTA (principles)
CAPA implementation
Equipment calibration & validation
Instrument qualification
English
native/bilingual
German
intermediate, actively learning
Hindi
native
Malayalam
native

Einsatzorte

Einsatzorte

Deutschland
möglich

Projekte

Projekte

1 year 7 months
2024-05 - 2025-11

Maintained continuous audit-readiness

Laboratory Technician III
Laboratory Technician III
  • Maintained continuous audit-readiness across ISO 13485, GxP, and GMP frameworks, achieving zero deviations in all internal and external audits over 18 months in a high-throughput regulated environment.
  • Implemented CAPA workflows to investigate and resolve process deviations, reducing error scope by 10% through systematic root-cause analysis, corrective planning, and preventive action documentation.
  • Generated and maintained customised analysis reports and sample documentation using LIMS and ELN, reducing data retrieval time by 40% and ensuring full traceability across 10,000?15,000 daily samples.
  • Contributed to a custom automated aliquoting project using Hamilton robotic systems, improving throughput and precision by 20% through process optimisation and structured documentation.
  • Executed rigorous photometric QC analysis for product release and calibrated 7 instruments including pipetting robots, centrifuges, and spectrophotometers; managed just-in-time laboratory inventory.
  • Conducted PBMC isolation and blood fractionation on irreplaceable biological samples, ensuring 100% traceability and sterile handling under strict SOP and biosafety constraints. 
Azenta Germany GmbH; Griesheim, Germany | Fixed-term contract
8 months
2023-10 - 2024-05

Characterised biological material behaviour across complex matrices

Master?s Thesis Researcher
Master?s Thesis Researcher
  • Characterised biological material behaviour across complex matrices (textiles, swab samples) using modified phenol?chloroform extraction and RNeasy Mini Kits, including purity and integrity assessment at each stage.
  • Executed end-to-end transcriptome analysis: cDNA library preparation, quality assessment, sequencing on Illumina MiSeq and Oxford Nanopore, QC, contaminant removal, and downstream assembly.
  • Applied variant detection and sequence assembly pipelines independently, developing practical command of error correction and functional interpretation of sequencing outputs.
  • Maintained ?80°C cold chain management and strict autoclave sterilisation protocols throughout the full experimental cycle. 
Hochschule Furtwangen University; Villingen-Schwenningen, Germany
8 months
2023-02 - 2023-09

Designed and executed PCR experiments

Student Research Assistant
Student Research Assistant
  • Designed and executed PCR experiments including primer design, thermal cycling, DNA extraction, gel electrophoresis, and gel imaging for molecular genetics research.
  • Prepared samples using differential and density gradient centrifugation; sterilised equipment and culture media by autoclave.
  • Compiled comprehensive technical reports supporting multidisciplinary research projects.
Hochschule Furtwangen University; Villingen-Schwenningen, Germany
2 months
2020-09 - 2020-10

Evaluated 5+ biocides against pathogenic cultures

Intern / Research Associate
Intern / Research Associate
  • Evaluated 5+ biocides against pathogenic cultures, identifying two high-efficacy agents that reduced laboratory contamination rates by 50%.
  • Improved antimicrobial screening efficiency by 25% through optimisation of agar well diffusion and cross streak methodologies. 
BioLim Centre for Science & Technology; Chennai, India

Aus- und Weiterbildung

Aus- und Weiterbildung

2022 ? 2024

MSc Precision Medicine and Diagnostics

Hochschule Furtwangen University, Germany | Honor Roll 2024, top 10%


2018 ? 2021

BSc Biotechnology

P.D. Patel Institute of Applied Sciences, Gujarat, India | Honour Roll 2021, top 5%

Kompetenzen

Kompetenzen

Top-Skills

Laboratory Automation ? Hamilton Robotic Systems Nucleic Acid Technologies ? NGS & Molecular Diagnostics PCR / qPCR ? primer design GxP / GMP Compliance & Audit Readiness Gel electrophoresis & gel imaging Reverse transcription & cDNA library preparation PBMC isolation & blood fractionation Bacterial & pathogenic microbial cultures Mammalian cell culture principles (CHO HEK293) Autoclave sterilisation & S1 biosafety lab operations Cold chain & cryogenic sample management (?80°C) Culture media preparation Spectrophotometry / photometric analysis Transcriptome assembly & QC Contaminant removal & error correction Density gradient & differential centrifugation HPLC (principles) ELISA (principles) Protein analytics & purification ? ÄKTA (principles) CAPA implementation Equipment calibration & validation Instrument qualification

Produkte / Standards / Erfahrungen / Methoden

PROFESSIONAL SUMMARY

Life scientist with an MSc in Precision Medicine and Diagnostics and hands-on experience in regulated laboratory environments governed by ISO 13485, GxP, and GMP frameworks. Brings a strong foundation in biological material characterisation, rigorous QC documentation, and cross-functional communication across R&D and compliance-sensitive settings. Achieved zero audit deviations over 18 months and reduced process error scope by 10% through systematic CAPA analysis. Prepared to apply that discipline to biocompatibility verification and ISO 10993 assessment in active medical device development. 


SKILLS & COMPETENCIES

Quality & Compliance

  • ISO 13485, ISO 10993 (series foundations)
  • GxP, GMP, GLP, SOP development
  • CAPA
  • root-cause analysis
  • audit readiness
  • equipment calibration & validation


Biological Characterisation

  • Nucleic acid extraction & purity assessment
  • PBMC isolation
  • blood fractionation
  • photometric analysis
  • cell/tissue handling
  • S1 biosafety lab


Verification & Documentation

  • Hardware verification support
  • product & project documentation
  • LIMS, ELN, ERP/SAP
  • customised reporting
  • full traceability management 


Laboratory Techniques

  • PCR/qPCR
  • primer design
  • gel electrophoresis
  • centrifugation
  • autoclave sterilisation
  • Hamilton robotic liquid handling
  • cold chain management (?80°C) 

Einsatzorte

Einsatzorte

Deutschland
möglich

Projekte

Projekte

1 year 7 months
2024-05 - 2025-11

Maintained continuous audit-readiness

Laboratory Technician III
Laboratory Technician III
  • Maintained continuous audit-readiness across ISO 13485, GxP, and GMP frameworks, achieving zero deviations in all internal and external audits over 18 months in a high-throughput regulated environment.
  • Implemented CAPA workflows to investigate and resolve process deviations, reducing error scope by 10% through systematic root-cause analysis, corrective planning, and preventive action documentation.
  • Generated and maintained customised analysis reports and sample documentation using LIMS and ELN, reducing data retrieval time by 40% and ensuring full traceability across 10,000?15,000 daily samples.
  • Contributed to a custom automated aliquoting project using Hamilton robotic systems, improving throughput and precision by 20% through process optimisation and structured documentation.
  • Executed rigorous photometric QC analysis for product release and calibrated 7 instruments including pipetting robots, centrifuges, and spectrophotometers; managed just-in-time laboratory inventory.
  • Conducted PBMC isolation and blood fractionation on irreplaceable biological samples, ensuring 100% traceability and sterile handling under strict SOP and biosafety constraints. 
Azenta Germany GmbH; Griesheim, Germany | Fixed-term contract
8 months
2023-10 - 2024-05

Characterised biological material behaviour across complex matrices

Master?s Thesis Researcher
Master?s Thesis Researcher
  • Characterised biological material behaviour across complex matrices (textiles, swab samples) using modified phenol?chloroform extraction and RNeasy Mini Kits, including purity and integrity assessment at each stage.
  • Executed end-to-end transcriptome analysis: cDNA library preparation, quality assessment, sequencing on Illumina MiSeq and Oxford Nanopore, QC, contaminant removal, and downstream assembly.
  • Applied variant detection and sequence assembly pipelines independently, developing practical command of error correction and functional interpretation of sequencing outputs.
  • Maintained ?80°C cold chain management and strict autoclave sterilisation protocols throughout the full experimental cycle. 
Hochschule Furtwangen University; Villingen-Schwenningen, Germany
8 months
2023-02 - 2023-09

Designed and executed PCR experiments

Student Research Assistant
Student Research Assistant
  • Designed and executed PCR experiments including primer design, thermal cycling, DNA extraction, gel electrophoresis, and gel imaging for molecular genetics research.
  • Prepared samples using differential and density gradient centrifugation; sterilised equipment and culture media by autoclave.
  • Compiled comprehensive technical reports supporting multidisciplinary research projects.
Hochschule Furtwangen University; Villingen-Schwenningen, Germany
2 months
2020-09 - 2020-10

Evaluated 5+ biocides against pathogenic cultures

Intern / Research Associate
Intern / Research Associate
  • Evaluated 5+ biocides against pathogenic cultures, identifying two high-efficacy agents that reduced laboratory contamination rates by 50%.
  • Improved antimicrobial screening efficiency by 25% through optimisation of agar well diffusion and cross streak methodologies. 
BioLim Centre for Science & Technology; Chennai, India

Aus- und Weiterbildung

Aus- und Weiterbildung

2022 ? 2024

MSc Precision Medicine and Diagnostics

Hochschule Furtwangen University, Germany | Honor Roll 2024, top 10%


2018 ? 2021

BSc Biotechnology

P.D. Patel Institute of Applied Sciences, Gujarat, India | Honour Roll 2021, top 5%

Kompetenzen

Kompetenzen

Top-Skills

Laboratory Automation ? Hamilton Robotic Systems Nucleic Acid Technologies ? NGS & Molecular Diagnostics PCR / qPCR ? primer design GxP / GMP Compliance & Audit Readiness Gel electrophoresis & gel imaging Reverse transcription & cDNA library preparation PBMC isolation & blood fractionation Bacterial & pathogenic microbial cultures Mammalian cell culture principles (CHO HEK293) Autoclave sterilisation & S1 biosafety lab operations Cold chain & cryogenic sample management (?80°C) Culture media preparation Spectrophotometry / photometric analysis Transcriptome assembly & QC Contaminant removal & error correction Density gradient & differential centrifugation HPLC (principles) ELISA (principles) Protein analytics & purification ? ÄKTA (principles) CAPA implementation Equipment calibration & validation Instrument qualification

Produkte / Standards / Erfahrungen / Methoden

PROFESSIONAL SUMMARY

Life scientist with an MSc in Precision Medicine and Diagnostics and hands-on experience in regulated laboratory environments governed by ISO 13485, GxP, and GMP frameworks. Brings a strong foundation in biological material characterisation, rigorous QC documentation, and cross-functional communication across R&D and compliance-sensitive settings. Achieved zero audit deviations over 18 months and reduced process error scope by 10% through systematic CAPA analysis. Prepared to apply that discipline to biocompatibility verification and ISO 10993 assessment in active medical device development. 


SKILLS & COMPETENCIES

Quality & Compliance

  • ISO 13485, ISO 10993 (series foundations)
  • GxP, GMP, GLP, SOP development
  • CAPA
  • root-cause analysis
  • audit readiness
  • equipment calibration & validation


Biological Characterisation

  • Nucleic acid extraction & purity assessment
  • PBMC isolation
  • blood fractionation
  • photometric analysis
  • cell/tissue handling
  • S1 biosafety lab


Verification & Documentation

  • Hardware verification support
  • product & project documentation
  • LIMS, ELN, ERP/SAP
  • customised reporting
  • full traceability management 


Laboratory Techniques

  • PCR/qPCR
  • primer design
  • gel electrophoresis
  • centrifugation
  • autoclave sterilisation
  • Hamilton robotic liquid handling
  • cold chain management (?80°C) 

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