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Senior QC Technician

DGN Technologies

Oceanside, California • 2d ago

Easy Apply

Contract, Third Party

$28 - $35

Senior Helpdesk Technician

Sun Harbor Advisors LLC

Remote • 5d ago

Easy Apply

Full-time

$60 - $90

Job Details

Skills

Biovia
LIMS/ELN
Laboratory Workflow Automation
Recipe Development
QC Laboratory
GMP/ISO
Data Integrity
BPMN
GDP
CSV
GAMP5
21 CFR Part 11
EU Annex 11
Chromatography
Spectrometry
Coulometry
Particle Analysis
Laboratory Process Design
Method Validation
Cleaning Validation
Instrument Qualification
Ph. Eur.
USP
ICH
MHRA
Empower
LabX
Chromeleon
MassHunter
OpenLab
Agile
Scrum
SAFe
Business Analysis
Software Development
Quality Control
Pharmaceutical Industry
Code Versioning

Biovia
LIMS/ELN
Laboratory Workflow Automation
Recipe Development
QC Laboratory
GMP/ISO
Data Integrity
BPMN
GDP
CSV
GAMP5
21 CFR Part 11
EU Annex 11
Chromatography
Spectrometry
Coulometry
Particle Analysis
Laboratory Process Design
Method Validation
Cleaning Validation
Instrument Qualification
Ph. Eur.
USP
ICH
MHRA
Empower
LabX
Chromeleon
MassHunter
OpenLab
Agile
Scrum
SAFe
Business Analysis
Software Development
Quality Control
Pharmaceutical Industry
Code Versioning

Summary

Description:

What you will do

Create automated laboratory workflows and support development of laboratory “recipes” within the Biovia software system.
Collaborate with business stakeholders to gather feedback and propose new functionalities
Report defects, test new software features, and support system improvements
Design and enhance reporting functionalities and interfaces within laboratory systems
Work with end users to design and optimize complex workflows and processes
Prepare and maintain documentation in regulated laboratory environments

What we are looking for

An individual with the ability to create new and/or modify existing Biovia based recipes for use within the Quality Control Laboratory.
Domain knowledge in biotechnology, chemistry, biochemistry, microbiology, analytical chemistry, or related fields
Experience working in a regulated laboratory environment (ISO or GMP)
Experience with laboratory techniques such as chromatography, spectrometry, coulometry, or particle analysis
Good understanding of laboratory processes (certification, IPC, sample cycle, etc.)
Experience in creating documentation (GDP)
BPMN fundamentals and ability to work with end users on workflow design
Understanding of Data Integrity concepts
Strong analytical, communication, and problem-solving skills
Proactive attitude and ability to work effectively in international teams

Nice to have

Knowledge of Ph. Eur, USP, ICH, MHRA, and related standards
Experience with LIMS systems (LabWare, CoreLims, LabVantage)
Experience with ELN/LES systems (especially ONELab from Biovia)
Experience with laboratory software such as Empower, LabX, Chromeleon, MassHunter, or OpenLab
Knowledge of CSV, GAMP5, 21 CFR Part 11, and EU Annex 11
Experience in pharmaceutical method validation, cleaning validation, or instrument qualification
Familiarity with Agile methodologies (Scrum, SAFe) and Business Analysis concepts
Understanding of code versioning concepts

Education and Experience

BS/BA degree and 8-11 years experience in Computer Science (Software Development) or Life Science (Biology, Biochemistry) or Equivalent
Masters degree and 6-9 years experience in Computer Science (Software Development) or Life Science (Biology or Biochemistry) or Equivalent
PhD/JD and 3-6 years experience in Computer Science (Software Development) or Life Science (Biology or Biochemistry) or Equivalent
Minimum 8 years pharmaceutical experience
Minimum 5 years experience in Software Development role or Quality Control.

Work Environment

Works in an office environment.
May be exposed to hazardous materials and chemicals.
May be required to lift up to 30lbs

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 10110849
Position Id: 1744-10990-1786755904
Posted 2 days ago

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Job Details

Skills

Biovia
LIMS/ELN
Laboratory Workflow Automation
Recipe Development
QC Laboratory
GMP/ISO
Data Integrity
BPMN
GDP
CSV
GAMP5
21 CFR Part 11
EU Annex 11
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Spectrometry
Coulometry
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Method Validation
Cleaning Validation
Instrument Qualification
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Agile
Scrum
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Software Development
Quality Control
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Code Versioning

Biovia
LIMS/ELN
Laboratory Workflow Automation
Recipe Development
QC Laboratory
GMP/ISO
Data Integrity
BPMN
GDP
CSV
GAMP5
21 CFR Part 11
EU Annex 11
Chromatography
Spectrometry
Coulometry
Particle Analysis
Laboratory Process Design
Method Validation
Cleaning Validation
Instrument Qualification
Ph. Eur.
USP
ICH
MHRA
Empower
LabX
Chromeleon
MassHunter
OpenLab
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Scrum
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Business Analysis
Software Development
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Summary

Description:

What you will do

Create automated laboratory workflows and support development of laboratory “recipes” within the Biovia software system.
Collaborate with business stakeholders to gather feedback and propose new functionalities
Report defects, test new software features, and support system improvements
Design and enhance reporting functionalities and interfaces within laboratory systems
Work with end users to design and optimize complex workflows and processes
Prepare and maintain documentation in regulated laboratory environments

What we are looking for

An individual with the ability to create new and/or modify existing Biovia based recipes for use within the Quality Control Laboratory.
Domain knowledge in biotechnology, chemistry, biochemistry, microbiology, analytical chemistry, or related fields
Experience working in a regulated laboratory environment (ISO or GMP)
Experience with laboratory techniques such as chromatography, spectrometry, coulometry, or particle analysis
Good understanding of laboratory processes (certification, IPC, sample cycle, etc.)
Experience in creating documentation (GDP)
BPMN fundamentals and ability to work with end users on workflow design
Understanding of Data Integrity concepts
Strong analytical, communication, and problem-solving skills
Proactive attitude and ability to work effectively in international teams

Nice to have

Knowledge of Ph. Eur, USP, ICH, MHRA, and related standards
Experience with LIMS systems (LabWare, CoreLims, LabVantage)
Experience with ELN/LES systems (especially ONELab from Biovia)
Experience with laboratory software such as Empower, LabX, Chromeleon, MassHunter, or OpenLab
Knowledge of CSV, GAMP5, 21 CFR Part 11, and EU Annex 11
Experience in pharmaceutical method validation, cleaning validation, or instrument qualification
Familiarity with Agile methodologies (Scrum, SAFe) and Business Analysis concepts
Understanding of code versioning concepts

Education and Experience

BS/BA degree and 8-11 years experience in Computer Science (Software Development) or Life Science (Biology, Biochemistry) or Equivalent
Masters degree and 6-9 years experience in Computer Science (Software Development) or Life Science (Biology or Biochemistry) or Equivalent
PhD/JD and 3-6 years experience in Computer Science (Software Development) or Life Science (Biology or Biochemistry) or Equivalent
Minimum 8 years pharmaceutical experience
Minimum 5 years experience in Software Development role or Quality Control.

Work Environment

Works in an office environment.
May be exposed to hazardous materials and chemicals.
May be required to lift up to 30lbs

Dice Id: 10110849
Position Id: 1744-10990-1786755904
Posted 2 days ago

Fitment

Dice Job Match Score™

📋 Comparing job requirements...

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

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