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Senior Labware Lims Developer Jobs in North Carolina

Biogen

NC · On-site

$93K - $121K/yr

The Senior Automation Engineer I will support Syncade (MES) system administration within a GMP ... DeltaV, PI, and Infobatch, CMMS, Oracle, Veeva, LIMS * Provide technical support during ...

FUJIFILM Biotechnologies

Collaborate with cross-functional partners-including end users, Validation, Labware Specialists ... Engineering, or related science field with 5+ years of experience ORMaster's in Chemistry ...

ALLIANCE BIOTECH SOLUTIONS LLC

CSV Engineer

Raleigh, NC · On-site

Description The Senior Computer System Validation (CSV) Engineer is responsible for leading the ... LIMS, MES, ERP, PI Historian, and related GxP systems. Verify data integrity, security, audit trail ...

Alliance Biotech Solutions LLC

CSV Engineer

Raleigh, NC · On-site

The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of ... LIMS, MES, ERP, PI Historian, and related GxP systems. · Verify data integrity, security, audit ...

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Senior Labware Lims Developer information

What is a Senior Labware LIMS Developer?

A Senior Labware LIMS Developer is an experienced software professional who specializes in designing, developing, and maintaining Laboratory Information Management Systems (LIMS) using LabWare software. They work closely with laboratory staff and IT teams to customize and optimize LIMS solutions, ensuring efficient data management and compliance with industry regulations. These developers often lead complex projects, troubleshoot technical issues, and mentor junior team members to enhance laboratory workflows.

What are the key skills and qualifications needed to thrive as a Senior Labware LIMS Developer?

To thrive as a Senior Labware LIMS Developer, you need expertise in software development, database management, and extensive experience with LabWare LIMS, often supported by a degree in computer science, bioinformatics, or a related field. Proficiency in LabWare scripting, SQL, JavaScript, and familiarity with laboratory workflows and compliance standards like GxP are typically required, along with relevant certifications. Strong analytical thinking, problem-solving, and effective communication skills enable you to translate complex lab requirements into robust technical solutions. These competencies are essential for delivering reliable, scalable LIMS implementations that support scientific operations and regulatory compliance.

What are the typical collaboration points between a Senior Labware LIMS Developer and laboratory staff during system enhancements?

A Senior Labware LIMS Developer frequently collaborates with laboratory staff to gather requirements, validate workflows, and ensure that system enhancements align with actual lab processes. This involves conducting user interviews, participating in design reviews, and providing training or support during user acceptance testing. Regular communication helps bridge gaps between technical capabilities and lab needs, resulting in solutions that improve efficiency and data integrity within the lab environment.

What is the difference between Senior Labware Lims Developer vs Labware Lims Analyst?

AspectSenior Labware Lims DeveloperLabware Lims Analyst
CredentialsTypically requires a degree in life sciences, computer science, or related field; certifications in Labware LIMS are commonOften holds similar degrees; certifications in Labware LIMS may be preferred but less emphasized
Work EnvironmentFocuses on software development, customization, and integration within laboratory settingsPrimarily analyzes data, supports system users, and ensures data integrity in labs
Employer & Industry UsageUsed by biotech, pharma, and clinical labs for system development and maintenanceEmployed in similar industries for data analysis and system support roles

The Senior Labware Lims Developer primarily focuses on developing and customizing LIMS software, while the Labware Lims Analyst concentrates on data analysis and system support. Both roles require relevant certifications and work within laboratory environments, but their core responsibilities differ significantly.

What are the most commonly searched types of Labware Lims Developer jobs in North Carolina?

The most popular types of Labware Lims Developer jobs in North Carolina are:

What are popular job titles related to Senior Labware Lims Developer jobs in North Carolina?

For Senior Labware Lims Developer jobs in North Carolina, the most frequently searched job titles are:

What job categories do people searching Senior Labware Lims Developer jobs in North Carolina look for?

The top searched job categories for Senior Labware Lims Developer jobs in North Carolina are:

What cities in North Carolina are hiring for Senior Labware Lims Developer jobs?

Cities in North Carolina with the most Senior Labware Lims Developer job openings:

Senior Labware Lims Developer jobs near you
Infographic showing various Senior Labware Lims Developer job openings in North Carolina as of August 2026, with employment types broken down into 77% Full Time, 7% Part Time, 1% Temporary, 14% Contract, and 1% Nights. Highlights an 80% Physical, 6% Hybrid, and 14% Remote job distribution.

Sr Engineer I, Automation (Syncade MES)

Biogen

NC • On-site

$93K - $121K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago

Biogen rating

9.3

Company rating: 9.3 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

3rd of 86 rated pharmaceutical

Job description

About This Role
We are seeking an experienced technical contributor to join our Automation Systems Engineering team at the Biogen RTP Bio site. The Senior Automation Engineer I will support Syncade (MES) system administration within a GMP-regulated manufacturing environment. This role operates with a high degree of independence and is accountable for ensuring system reliability, supporting manufacturing execution, and driving continuous improvement initiatives. The Senior Automation Engineer I will be a subject matter expert for Syncade, capable of leading small-to-moderate complexity initiatives to influence cross-functional outcomes.
What You'll Do
  • Act as system administrator/SME for Syncade (MES), including configuration, maintenance, troubleshooting, and lifecycle management
  • Own and support Syncade Application and the relevant infrastructure to enable electronic batch record (eBR) workflows, recipe configuration, and exception handling
  • Ensure system availability, performance, and data integrity to support GMP manufacturing operations
  • Lead root cause investigations and implement corrective/preventive actions for MES-related deviations
  • Manage user access, security roles, and audit trail reviews in compliance with GxP and cybersecurity requirements
  • Execute and support change controls, including system updates, enhancements, and validation deliverables (IQ/OQ/PQ)
  • Drive continuous improvement efforts to enhance system usability, reliability, and operational efficiency
  • Support integration and data flow between Syncade and other automation and Enterprise systems, e.g. DeltaV, PI, and Infobatch, CMMS, Oracle, Veeva, LIMS
  • Provide technical support during manufacturing operations, including off-hours support as required

Who You Are
You are a meticulous professional with a strong foundation in automation / manufacturing systems engineering, particularly in biopharmaceutical settings. Your analytical mindset and problem-solving skills empower you to tackle complex challenges independently. You thrive in collaborative environments, easily engaging with diverse teams to achieve shared goals. Your
dedication to operational excellence and compliance ensures that systems run smoothly and efficiently.
Required Skills
  • Bachelor's degree in Engineering
  • 5-8+ years of automation engineering experience in a regulated environment (GMP preferred)
  • Minimum of 3 years of experience with Syncade/MES Infrastructure, workflows, eBR design, and manufacturing process support
  • Strong understanding of GxP compliance, data integrity, and change control processes
  • Proven ability to independently troubleshoot and resolve complex technical issues

Preferred Skills
  • Experience with Emerson DeltaV (DCS) integration and support
  • Experience with AVEVA PI System for data collection and analytics
  • Familiarity with Infobatch for batch reporting
  • Participation in system upgrades, tech transfers, or manufacturing modernization initiatives

Job Level: Professional
Additional Information
The base compensation range for this role is: $93,000.00-$121,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

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At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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