Referso Jobs

Lab Transformation Consultant

Accenture · Posted Nov 6, 2026

Open

London, England, United Kingdom

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Lab Transformation Consultant

Accenture · Posted Nov 6, 2026

Open

London, England, United Kingdom

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Field Service Specialist I

Waters Corporation · Posted Nov 5, 2026

Open

Raleigh, North Carolina, United States
On-site
Full-time · Entry
2+ years

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Provide technical expertise on Waters' innovative product suite (LC, LC/MS, HPLC/UPLC, SFC) for multiple customer laboratories spanning across Pharmaceutical & Life Sciences, Chemical Materials, Clinical, Food, Environmental, Forensics, Academia and Government industries.

Responsibilities

Installation, performance maintenance, troubleshoot and support Waters' product suite (LC, LC/MS, HPLC/UPLC, SFC, Informatics)
Establish and maintain effective relationships with external and internal customers ensuring their success
Lead customer expectations, by communicating work performed and providing follow up plan if needed
Ensure customer compliance regulations are followed
Deliver system level training at customer sites

Requirements

BS/BA in Chemistry or Biology, engineering or other science related field
Nice to have: Waters product suite (LC, LC/MS, HPLC/UPLC, SFC, Informatics)
Nice to have: CDS, SDMS, LIM, ELN

Skills

Scientific instrumentation maintenance Troubleshooting Scientific application workflow Valid Driver's License

Consultant, Scientific and Laboratory Informatics

Accenture Infrastructure and Capital Projects, LLC · Posted Nov 4, 2026

Open

California, United States +13 more
Full-time · Associate
$54K–$206K per year
3+ years

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Consultant focused on scientific and laboratory informatics helping clients achieve digital and AI laboratory transformation using technologies like LIMS, ELN, and IoT.

Locations (14)

California, United States
Colorado, United States
Connecticut, United States
District of Columbia, United States
Illinois, United States

Sr Scientist - Biologics Drug Product Development

Regeneron · Posted Nov 5, 2026

Open

Tarrytown, New York, United States
On-site
Full-time · Senior
$112K–$183K per year
0+ years

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Lead and execute drug product development activities from candidate selection through commercialization, applying biochemical, biophysical, and microbiology principles to formulate, analyze, and optimize biologic drug modalities.

Compensation

Salary Range (annually) $112,100.00 - $182,900.00

Responsibilities

Design and conduct formulation development and stability studies
Perform analytical development and microbial analysis
Develop and transfer new technologies and processes
Prepare and deliver presentations, SOPs, and patents
Maintain accurate laboratory records and comply with data integrity procedures

Requirements

Ph.D. in Pharmaceutical Science, Biochemistry, Chemistry, Microbiology, Biophysics, Engineering, or related field
BS or MS with 8-10 years of experience, or Ph.D. with 0-3 years of experience

Skills

formulation development stability studies compatibility testing analytical development process development

Director– Quality Management Systems (QMS) & Digital Quality Governance

Merck & Co., Inc. · Posted Nov 5, 2026

Open

Wilmington, Delaware, United States
Hybrid
Manager
$173K–$273K per year
10–15 years

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Lead and oversee the transformation of Quality Management Systems within a complex laboratory environment, driving digital modernization, regulatory compliance, and operational excellence.

Compensation

$173,200.00 - $272,600.00

Responsibilities

Architect and modernize QMS architecture
Lead QMS integration strategy
Oversee digital quality governance
Ensure regulatory compliance and inspection readiness
Manage cross-functional QMS workstream

Requirements

Bachelor’s degree in Chemistry, Biochemistry, Pharmacy, Engineering, Life Sciences, or related discipline
Nice to have: Analytical Testing
Nice to have: Change Leadership
Nice to have: Program Governance

Skills

Quality Systems Expertise Digital & Laboratory Systems Acumen Validation & Compliance Mastery Governance & Program Execution Analytical Development

Director– Quality Management Systems (QMS) & Digital Quality Governance

Merck · Posted Nov 5, 2026

Open

Wilmington, Delaware, United States
Hybrid
Full-time · Director
$173K–$273K per year
10–15 years

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Strategic and operational leadership for the QMS workstream within a complex, enterprise-level laboratory transformation program, focusing on architecting and deploying a modernized, digitized Quality Management System.

Compensation

$173,200 - $272,600

Responsibilities

Define, lead, and execute the QMS integration strategy for the lab transformation initiative.
Oversee harmonization and evolution of quality processes including deviation management, investigations, CAPA, change control, risk management (ICH Q9), and computerized systems validation (CSV/CSA).
Oversee the eQMS and review/understand underlying code to ensure compliance.
Partner with IT/Digital Quality and Automation engineers to embed Data Integrity by Design (ALCOA+) and Computer Software Assurance (CSA) principles.
Ensure all modernized QMS processes, policies, and SOPs comply with global cGMP regulations (FDA 21 CFR Part 11/210/211, EU Annex 11, ICH Q9/Q10, WHO).

Requirements

Bachelor’s degree in Chemistry
Biochemistry
Pharmacy
Engineering
Life Sciences

Skills

Quality Management Systems (QMS)cGMP QC laboratory

Field Service Specialist II

Waters Corporation · Posted Nov 4, 2026

Open

Indianapolis, Indiana, United States
Hybrid
Full-time · Mid
2+ years

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Providing technical expertise on Waters' innovative product suite (LC, LC/MS, HPLC/UPLC, SFC) for multiple customer laboratories across various industries.

Responsibilities

Installation, performance maintenance, troubleshoot and support Waters' product suite (LC, LC/MS, HPLC/UPLC, SFC, Informatics)
Establish and maintain effective relationships with external and internal customers ensuring their success
Lead customer expectations, by communicating work performed and providing follow up plan if needed
Ensure customer compliance regulations are followed
Deliver system level training at customer sites

Requirements

BS/BA in Chemistry or Biology, engineering or other science related field
Nice to have: LC, LC/MS, HPLC/UPLC, SFC, Informatics

Skills

scientific instrumentation troubleshooting scientific application workflow knowledge scientific software systems (CDS, SDMS, LIM, ELN)Valid Driver's License

Field Service Specialist II

Waters Corporation · Posted Nov 4, 2026

Open

Salt Lake City, Utah, United States
Hybrid
Full-time · Mid
2+ years

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Provide technical expertise on Waters’ product suite (LC, LC/MS, HPLC/UPLC, SFC) for customer laboratories across various industries.

Responsibilities

Installation, performance maintenance, troubleshoot and support Waters' product suite
Establish and maintain effective relationships with external and internal customers
Manage customer expectations, by communicating work performed and providing follow up plan if needed
Ensure customer compliance regulations are followed
Deliver system level training at customer sites

Requirements

BS/BA in Chemistry or Biology, engineering or other science related field

Skills

installation performance maintenance troubleshooting support scientific instrumentation Waters product suite valid driver's license

Global QC labs Application Engineer

Valce Talent Solutions · Posted Nov 3, 2026

Open

Mexico City, Mexico City, Mexico
Hybrid
5+ years

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Application Engineer responsible for QC lab systems, including LIMS, SDMS, and Empower, ensuring validation, system upgrades, and stakeholder communication.

Responsibilities

Support technical upgrades and impact assessments
Maintain CMDB for relevant systems
Provide technical and functional feedback during audits
Work with privacy and security teams on data requests
Manage vendor relationships and budgets

Requirements

Bachelor’s degree in relevant biotech area (e.g. pharmaceutical- and bio technology)
Nice to have: Agile
Nice to have: CI/CD
Nice to have: PL/SQL
Nice to have: Python

Skills

CDS LIMS SDMS CSV GAMP 5 CMDB system audit privacy laws vendor management

USA_Technical Writer

Varite, Inc · Posted Nov 3, 2026

Open

San Francisco, California, United States
$58–$62 per hour
4–7 years

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Technical writer responsible for testing and validation of laboratory instrument integrations and data pipelines in a cell and gene therapy environment.

Compensation

Pay Rate Range: $58.33 - 62.12/hr.

Responsibilities

Demonstrate detail-oriented work with high accuracy
Explain complex concepts with clarity and simplicity
Proactively lead testing effort
Work in cross-functional and global team
Demonstrate knowledge of GxP requirements and documentation standards

Skills

Lab Informatics LIMS CDS ELN SDMS API testing JSON XML Tetra Data Platform Computer System Validation

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