Referso Jobs

Perform laboratory tests on various products including dairy and environmental samples
Provide accurate test results using predetermined, approved methods of analysis
Ensure results are communicated to internal customers in a timely and efficient manner
Collaborate in the support of internal and external programs
Record data and communicate results (entry into Labware, D365)

Requirements

High School or GED
Associate Degree in Chemistry, Microbiology or other related field

Skills

laboratory testing dairy testing environmental sampling data entry Labware D365

Senior IT GxP Technical Analyst

ConsultNet · Posted Nov 5, 2026

Open

Rockville, Maryland, United States
Hybrid
Full-time · Senior
Salary / Pay Rate: DOE
6+ years

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Lead the design, development, and delivery of IT solutions and applications that run the company's bioanalytical laboratory, ensuring compliance with GxP and regulatory standards.

Responsibilities

Serve as the senior technical authority for bioanalytical laboratory systems
Gather, analyze, and document business, laboratory, and data requirements
Design, configure, develop, and deploy GxP solutions
Own the technical side of the system lifecycle
Produce technical validation documentation

Requirements

Bachelor's degree in Information Technology, Computer Science, Information Systems, Bioinformatics, or a related discipline
Nice to have: IT experience in a high throughput clinical research organization (CRO)
Nice to have: Experience with bioanalytical workflows
Nice to have: Mentoring or providing technical review for other IT staff

Skills

LIMS implementation and administration SQL Reporting tools APIs and web services Scripting or programming language

Sr. Lab Technician

Tropicana Brands Group · Posted Nov 5, 2026

Open

Bradenton, Florida, United States
On-site
Full-time · Mid
1+ years

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The role is a highly qualified Quality Control Sr Lab Technician to support the Bradenton, FL, Supply Chain team to ensure the company’s goals and initiatives are met.

Responsibilities

Perform analytical chemistry procedures in accordance with prescribed methods and training, including HPLC, GC, and atomic absorption analysis.
Prepare reagents for laboratory testing.
Calibrate, prepare, and maintain equipment for laboratory analysis.
Collect samples in accordance with the laboratory sampling plan or special requests.
Monitor equipment performance and build proficiency in troubleshooting instruments.

Requirements

High school diploma or GED
Science-related degree preferred
Nice to have: Labware

Skills

liquid chromatography gas chromatography atomic absorption methods microbiology pour plate methods basic laboratory skills math

Senior QA Specialist - CSV

Johnson & Johnson · Posted Nov 4, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Senior
6+ years

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Seeking a highly qualified Senior QA Specialist - CSV to join a new Biotherapeutics Manufacturing facility, focusing on CSV programs, data integrity, and risk-based validation for greenfield site technologies.

Responsibilities

Author, implement, and maintain site CSV and data integrity procedures
Contribute to the Validation Master Plan, computerized system inventory, and GxP/criticality assessments
Represent Quality Assurance on qualification teams across requirements, design review, construction, commissioning, qualification, and implementation
Provide consulting to the project management team to ensure appropriate quality systems are in place for new systems
Apply GAMP 5 (2nd Edition) critical thinking, ICH Q9(R1), and ASTM E2500 principles

Requirements

Bachelor's degree in a scientific, engineering, or computer science discipline
Nice to have: Sterile fill-finish
Nice to have: Isolator
Nice to have: RABS automation
Nice to have: Automated visual inspection

Skills

Computer System Validation (CSV)Data Integrity GxP Pharmaceutical industry

Senior QA Specialist - CSV

6084-Janssen Research & Development Legal Entity · Posted Nov 4, 2026

Open

Wilson, North Carolina, United States
Senior
6+ years

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Senior QA Specialist focused on CSV and data integrity at a new Biotherapeutics Manufacturing facility.

Responsibilities

Author, implement, and maintain site CSV and data integrity procedures
Represent QA on qualification teams across design review, construction, commissioning, qualification, and implementation
Apply GAMP 5, ICH Q9, ASTM E2500 principles for risk-based validation
Review and approve URS, FRS, HDS, SDS, configuration specifications, testing plans, and validation reports
Ensure deviations and CAPAs are documented and closed

Requirements

Bachelor's degree in a scientific, engineering, or computer science discipline
Nice to have: Validation experience with sterile fill-finish, isolator or RABS automation
Nice to have: Experience with automated visual inspection
Nice to have: Experience with combination products or device assembly
Nice to have: MES/electronic batch record experience

Skills

QA oversight of CSV for automated manufacturing equipment and systems GAMP 5 (2nd Edition) knowledge 21 CFR Part 11 compliance

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Engineer Tech V (Lead)

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Senior IT GxP Technical Analyst

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Sr. Lab Technician

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Senior QA Specialist - CSV

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Senior QA Specialist - CSV

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Labware jobs

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