Implementation Specialist
Fort Wayne, IN · On-site +1
... or remote technical seminars. • Resolve software and related hardware issues for current ... written and verbal communication, client consulting, and time-management skills. • Ability to ...
Implementation Specialist
Fort Wayne, IN · On-site +1
... or remote technical seminars. • Resolve software and related hardware issues for current ... written and verbal communication, client consulting, and time-management skills. • Ability to ...
Quality Auditor - Pharmaceutical
Churubusco, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Churubusco, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Fort Wayne, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Fort Wayne, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Evansville, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Evansville, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Warren, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Warren, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
South Bend, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
South Bend, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Indianapolis, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Indianapolis, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Carmel, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Quality Auditor - Pharmaceutical
Carmel, IN · Remote
$1.3K/day
... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...
Senior Engineer, Process Validation
Indianapolis, IN · On-site +1
$100K - $130K/yr
... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...
Senior Engineer, Process Validation
Indianapolis, IN · On-site +1
$100K - $130K/yr
... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...
Senior Engineer, Process Validation
Indianapolis, IN · On-site +1
$100K - $130K/yr
... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...
Senior Engineer, Process Validation
Indianapolis, IN · On-site +1
$100K - $130K/yr
... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...
Program Manager, Medical & Scientific Affairs (IVD, Medical Device)
Indianapolis, IN · On-site +1
$130K - $145K/yr
... fully remote. In this role, you will have the opportunity to: * Lead key projects and cross ... Excellent interpersonal skills, both verbal and written * Excellent organizational skills and ...
New
Program Manager, Medical & Scientific Affairs (IVD, Medical Device)
Indianapolis, IN · On-site +1
$130K - $145K/yr
... fully remote. In this role, you will have the opportunity to: * Lead key projects and cross ... Excellent interpersonal skills, both verbal and written * Excellent organizational skills and ...
New
... biologics, equipment, and related services. Leads contract development, negotiation support ... Excellent verbal and written communication skills, including the ability to communicate effectively ...
... biologics, equipment, and related services. Leads contract development, negotiation support ... Excellent verbal and written communication skills, including the ability to communicate effectively ...
... biologics, equipment, and related services. Leads contract development, negotiation support ... Excellent verbal and written communication skills, including the ability to communicate effectively ...
... biologics, equipment, and related services. Leads contract development, negotiation support ... Excellent verbal and written communication skills, including the ability to communicate effectively ...
This is a remote based role. Who You Are * You have a Minimum Associate's degree in Medical ... You have a customer service focus with strong verbal, written, and interpersonal communication ...
This is a remote based role. Who You Are * You have a Minimum Associate's degree in Medical ... You have a customer service focus with strong verbal, written, and interpersonal communication ...
Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innov...
Indianapolis, IN · On-site +1
$143K - $189K/yr
... Biology, or similar. * 10+ years of Regulatory CMC or technical CMC experience supporting clinical ... Demonstrated strong written, spoken and presentation communication skills. * Demonstrated ...
Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innov...
Indianapolis, IN · On-site +1
$143K - $189K/yr
... Biology, or similar. * 10+ years of Regulatory CMC or technical CMC experience supporting clinical ... Demonstrated strong written, spoken and presentation communication skills. * Demonstrated ...
We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological ... Remote * The willingness and ability to travel overnight * Requires driving a personal vehicle on ...
We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological ... Remote * The willingness and ability to travel overnight * Requires driving a personal vehicle on ...
Biology Writing Remote information
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Full-time
Medical, Dental, Vision, Life, Retirement
Posted yesterday
Job description
STARLIMS provides leading Laboratory Information Management System (LIMS) solutions that have served customers around the world for nearly 40 years. Our solution suite helps labs:
We value people who are curious, accountable, collaborative, and empathetic. Our teams are small, nimble and have a strong drive to succeed. If you are seeking to build your career while working on a technical product that our F500 customers describe as "critical to operational success,", you'll feel at home here.
About the Role:
The MODA-EM Implementation Specialist supports customer software deployments in GMP-regulated environments. You will work directly with clients to understand their QC Microbiology processes, configure and deploy MODA, and serve as a technical resource across the full implementation lifecycle. The role combines project coordination, hands-on configuration, training delivery, and customer support.
What You'll Do:
• Lead customer deployments in GMP-regulated environments, including project coordination, installation, documentation, and validation support.
• Deliver core team training, configuration activities, and end-user / administrative training.
• Conduct product demonstrations and on-site or remote technical seminars.
• Resolve software and related hardware issues for current customers via on-site visits, phone, email, and remote sessions.
• Partner with clients to align operational data, configurations, test methods, and reports with their QC Microbiology workflows.
• Contribute to documentation, training materials, and project plans.
• Manage multiple projects and assignments simultaneously, including pre-sales scoping and sales-to-service transitions.
What We're Looking For:
• Bachelor's degree, preferably in Life Sciences, Lab Systems, or Pharma IT.
• Excellent written and verbal communication, client consulting, and time-management skills.
• Ability to work independently across multiple concurrent projects.
You should have a core background in either QC Microbiology or Laboratory IT Systems, with complementary skills in the other:
QC Microbiology track:
• 3+ years in Quality Control microbiology or a related industry.
• BS in Biology, Microbiology, Chemistry, or related life-science field.
• Beginner-to-intermediate exposure to SQL Server, Oracle, Windows Server, Crystal Reports, Windows 10/11 administration, networking, software/testing lifecycle, or Azure DevOps.
Laboratory IT Systems track:
• 3+ years implementing software systems in regulated laboratory or pharmaceutical production environments (or software engineering experience).
• BS in Computer Science or related IT field.
• Experience implementing QC systems (environmental monitoring, final release, in-process control).
• Hands-on experience with one or more LIMS / lab software platforms such as LabWare, LabVantage SQL*LIMS or Sapphire, ThermoFisher Sample Manager, Novatek NOVA LIMS, Velquest SmartLab, Waters Empower, Labtronics Nexxis ELN, or LIMSLink.
• Foundational scientific knowledge in biology, microbiology, or chemistry, with willingness to deepen domain expertise.
At STARLIMS we offer market competitive benefits such as:
- Improve the reliability of sampling and testing
- Manage complex testing workflows and analytical methods
- Simplify compliance and support regulatory standards
- Unlock comprehensive reporting, monitoring, and analysis
We value people who are curious, accountable, collaborative, and empathetic. Our teams are small, nimble and have a strong drive to succeed. If you are seeking to build your career while working on a technical product that our F500 customers describe as "critical to operational success,", you'll feel at home here.
About the Role:
The MODA-EM Implementation Specialist supports customer software deployments in GMP-regulated environments. You will work directly with clients to understand their QC Microbiology processes, configure and deploy MODA, and serve as a technical resource across the full implementation lifecycle. The role combines project coordination, hands-on configuration, training delivery, and customer support.
What You'll Do:
• Lead customer deployments in GMP-regulated environments, including project coordination, installation, documentation, and validation support.
• Deliver core team training, configuration activities, and end-user / administrative training.
• Conduct product demonstrations and on-site or remote technical seminars.
• Resolve software and related hardware issues for current customers via on-site visits, phone, email, and remote sessions.
• Partner with clients to align operational data, configurations, test methods, and reports with their QC Microbiology workflows.
• Contribute to documentation, training materials, and project plans.
• Manage multiple projects and assignments simultaneously, including pre-sales scoping and sales-to-service transitions.
What We're Looking For:
• Bachelor's degree, preferably in Life Sciences, Lab Systems, or Pharma IT.
• Excellent written and verbal communication, client consulting, and time-management skills.
• Ability to work independently across multiple concurrent projects.
You should have a core background in either QC Microbiology or Laboratory IT Systems, with complementary skills in the other:
QC Microbiology track:
• 3+ years in Quality Control microbiology or a related industry.
• BS in Biology, Microbiology, Chemistry, or related life-science field.
• Beginner-to-intermediate exposure to SQL Server, Oracle, Windows Server, Crystal Reports, Windows 10/11 administration, networking, software/testing lifecycle, or Azure DevOps.
Laboratory IT Systems track:
• 3+ years implementing software systems in regulated laboratory or pharmaceutical production environments (or software engineering experience).
• BS in Computer Science or related IT field.
• Experience implementing QC systems (environmental monitoring, final release, in-process control).
• Hands-on experience with one or more LIMS / lab software platforms such as LabWare, LabVantage SQL*LIMS or Sapphire, ThermoFisher Sample Manager, Novatek NOVA LIMS, Velquest SmartLab, Waters Empower, Labtronics Nexxis ELN, or LIMSLink.
• Foundational scientific knowledge in biology, microbiology, or chemistry, with willingness to deepen domain expertise.
At STARLIMS we offer market competitive benefits such as:
- Competitive health and Wellness (medical, dental, and vision)
- Retirement plan with matching company contribution
- Life Insurance and Disability/Income Protection
About Starlims
Sourced by ZipRecruiter
Industry
Software development
Company size
201 - 500 Employees
Headquarters location
Hollywood, FL, US
Year founded
1987