Data Review – Specialist (Stability Protocol / Study Build Review)

Eurofins

Hinoba-an

On-site

PHP 4,380,000 - 6,884,000

Full time

6 days ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Eurofins Lancaster Laboratories is seeking a Data Reviewer Specialist to ensure accuracy and compliance of stability protocols and study builds prior to client release. This role includes a structured training progression to become a Stability Protocol Writer / Study Builder, gaining deep understanding of technical content and system workflows that impact client deliveries.

The position emphasizes analytical rigor, data integrity, and cross-functional collaboration to resolve issues while

Qualifications

  • Master’s degree in a scientific discipline (Chemistry, Biology, Pharmaceutical Sciences, or related field) or equivalent industry with 4-6 years of experience.
  • Experience or familiarity with GMP, data integrity expectations, and regulated laboratory environments.
  • Ability to learn and work effectively within LIMS or similar informatics systems.
  • Strong scientific comprehension and ability to interpret technical protocols, quotes, and study plans.
  • Exceptional attention to detail and commitment to data accuracy.
  • Strong communication skills with the ability to constructively collaborate and provide clear feedback.

Responsibilities

  • Perform detailed, independent review of stability protocols and study builds to ensure accuracy, completeness, and alignment with client expectations.
  • Confirm that all protocol parameters (e.g., storage conditions, pull points, test plans) are correctly entered and consistent with quotes and client-provided documents.
  • Verify compliance with GMP, internal SOPs, and industry guidelines.
  • Identify discrepancies, errors, or gaps and communicate effectively with Protocol Writers, Project Managers, and other stakeholders to resolve issues.
  • Ensure documentation is traceable, audit-ready, and maintained in accordance with data integrity principles (ALCOA+).
  • Support continuous improvements in review workflows, documentation standards, and system utilization.

Skills

Attention to detail
Data integrity
GMP familiarity
Communication skills

Education

Master’s degree in a scientific discipline

Tools

LIMS

Job description

Data Review – Specialist (Stability Protocol / Study Build Review)
  • Full-time

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.

Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 60 countries and about 63,000 staff.

Position Summary:Eurofins Lancaster Laboratories is seeking a highly analytical and quality‑driven Data Reviewer Specialist to ensure accuracy and compliance of all stability protocols and study builds prior to client release. This position plays a crucial role in safeguarding data integrity and ensuring that client expectations are consistently met.

This role includes a structured training progression: the individual will be fully trained as a Stability Protocol Writer / Study Builder prior to performing protocol and study review responsibilities. This ensures a deep understanding of both the technical content and system workflows that impact the quality of client deliveries.

Key Responsibilities
Training Phase – Protocol Writing & Study Building
  • Complete comprehensive training in protocol writing based on Eurofins‑generated quotes.
  • Learn and practice building stability studies within the LIMS system following client‑provided protocols.
  • Develop proficiency in interpreting client requirements, scientific documentation, and stability program workflows.
Primary Role – Data Review
  • Perform detailed, independent review of stability protocols and study builds to ensure accuracy, completeness, and alignment with client expectations.
  • Confirm that all protocol parameters (e.g., storage conditions, pull points, test plans) are correctly entered and consistent with both quotes and client-provided documents.
  • Verify compliance with GMP, internal SOPs, and industry guidelines.
  • Identify discrepancies, errors, or gaps and communicate effectively with Protocol Writers, Project Managers, and other stakeholders to resolve issues.
  • Ensure documentation is traceable, audit-ready, and maintained in accordance with data integrity principles (ALCOA+).
  • Support continuous improvements in review workflows, documentation standards, and system utilization.
Qualifications Required:
  • Master’s degree in a scientific discipline (Chemistry, Biology, Pharmaceutical Sciences, or related field) or equivalent industry with 4-6 years of experience.
  • Experience or familiarity with GMP, data integrity expectations, and regulated laboratory environments.
  • Ability to learn and work effectively within LIMS or similar informatics systems.
  • Strong scientific comprehension and ability to interpret technical protocols, quotes, and study plans.
  • Exceptional attention to detail and commitment to data accuracy.
  • Strong communication skills with the ability to constructively collaborate and provide clear feedback.
Key Candidate Attributes:
  • Self-motivation; excellent quality of work and attention to detail
  • Ability to communicate effectively with coworkers and internal/external clients
  • Ability to learn new tasks quickly and to move easily from task to task
  • Ability to handle prioritization and multiple tasks simultaneously
  • Ability to use a personal computer and learn necessary programs
  • Good communication skills (oral and written)
  • Organizational ability and good judgement
  • Science background/education and/or laboratory experience
  • Strong Math Skills
  • Logical Thinking, Good Reasoning Ability
  • Motivation to excel
  • Coaching/mentoring of peers
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Data Integrity Reviewer: Stability Protocol & Study Builder
Data Integrity Reviewer: Stability Protocol & Study Builder

Eurofins • Hinoba-an

On-site
PHP 4,380,000 - 6,884,000
Senior QA Specialist
Senior QA Specialist

Eurofins PSS Ireland Ltd • Hinoba-an

On-site
PHP 600,000 - 900,000
Pharma Document Reviewer
Pharma Document Reviewer

SGS Global Business Services Asia Inc. • Muntinlupa

On-site
PHP 600,000 - 900,000
Technical Customer Service
Technical Customer Service

HS Hiring Solutions Inc • Muntinlupa

On-site
PHP 360,000 - 480,000
Pharma Document Reviewer (Pharmaceutical Laboratory Experience is required)
Pharma Document Reviewer (Pharmaceutical Laboratory Experience is required)

SGS • Muntinlupa

On-site
PHP 900,000 - 1,300,000
Software Engineer
Software Engineer

Eurofins Scientific • Hinoba-an

On-site
PHP 400,000 - 700,000
Dot Net Fullstack Developer (Angular)
Dot Net Fullstack Developer (Angular)

Eurofins PSS Ireland Ltd • Hinoba-an

On-site
PHP 1,724,000 - 2,785,000
.Net Fullstack Engineer
.Net Fullstack Engineer

Eurofins PSS Ireland Ltd • Hinoba-an

On-site
PHP 1,194,000 - 1,990,000
Senior QA Specialist - GMP/GLP Compliance & Data Integrity
Senior QA Specialist - GMP/GLP Compliance & Data Integrity

Eurofins PSS Ireland Ltd • Hinoba-an

On-site
PHP 600,000 - 900,000
Pharma Document Reviewer
Pharma Document Reviewer

HS Hiring Solutions Inc • Muntinlupa

On-site
PHP 357,000 - 580,000
Performance Bonus
HMO
Job Training