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Frontage Laboratories logo

Laboratory Application Specialist

Frontage Laboratories·Exton, Pennsylvania

Full TimeOn Site0-2 yrsPosted 22 days ago
Practice for this role

Laboratory Application Specialist

About the role

The Laboratory Application Specialist supports daily laboratory operations, including sample management, instrument maintenance, and inventory control. They also assist project PIs with study documentation, data archival, and ensuring compliance with GLP/GCLP standards.

Laboratory Application Specialist-Large Molecule

Department

  • Biomarker &
  • Biologics
  • Location:
  • Onsite
  • Frontage 760 site
  • Employment
  • Type: Full-time

Frontage Laboratories

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position Summary

Laboratory Application Specialist-Large Molecule — a role that is to support lab operational and studies in a regulated (GLP/GCLP) research environment, including but not limited to documentation and data archival, sample handling, and other activities to support the studies. This role will support project PIs (principal investigator) with documentation, and coordination tasks, sample handling, ensuring compliance with GLP/GCLP standards and efficient study progression from setup to completion.

Key Responsibilities

  • 1. Laboratory operations support
  • Assist in daily laboratory activities such as sample management, labeling, preparation, and storage.
  • Maintain laboratory supplies, reagents, and consumables inventory to support ongoing projects.
  • Support instrument setup, calibration, and routine maintenance under supervision.
  • Other assigned tasks
  • 2. Study coordination and documents/Data archival
  • Support study PIs with project documentation and study setup tasks.
  • Assist in compiling data summaries, study logs, and project documents and reports.
  • Assist and maintain study records, worksheets, and study files according to SOPs.
  • Ensure all documents are reviewed, signed, and filed accurately.
  • Support document archival and retrieval activities per GLP/GCLP and company retention requirements.
  • Assist with electronic document uploads and metadata entry in LIMS or document management systems.
  • Follow all company SOPs, GLP/GCLP requirements, and data integrity standards.
  • 3. Continuous improvement
  • Identify opportunities to improve relative workflows or documentation processes.
  • Support implementation of digital tools for study tracking or data management.
  • Participate in cross-functional process improvement initiatives.

Qualifications

Education

• Bachelor’s degree in Life Sciences, Biology, Chemistry, Biochemistry, or a related scientific discipline.

Experience

  • 0–3 years of experience in lab assistant, document management, or records management (preferably in a regulated industry such as pharmaceutical, biotech, or CRO).
  • Experience with document control systems (e.g., SharePoint, Documentum, or similar).
  • Familiarity with regulatory documentation standards (e.g., GxP, GLP) preferred.

Skills

  • Strong organizational and time management abilities with attention to detail.
  • Excellent communication and interpersonal skills.
  • Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Analytical mindset with focus on process accuracy and compliance.

Core Competencies

  • Accountability and ownership
  • Process-oriented and detail-focused
  • Team collaboration and cross-functional coordination
  • Data and document integrity awareness
  • Problem-solving and initiative-taking

Preferred Qualifications

  • Experience in a laboratory, clinical, or regulatory documentation setting.
  • Knowledge of long-term data retention and archival best practices.
  • Familiarity with electronic archiving systems and metadata management.

Salary and Benefits

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Requirements

Candidates must hold a Bachelor’s degree in Life Sciences or a related scientific discipline. The role requires 0–3 years of experience in a laboratory or document management setting, preferably within a regulated industry.

  • bachelor degree
  • Documentation
  • Microsoft Office Suite
  • Organizational skills
  • Communication skills
  • LIMS
  • Attention to detail
  • Time management
  • Process improvement
  • Instrument maintenance
  • Data integrity
  • Laboratory operations
  • Regulatory documentation
  • Sample management
  • GLP compliance
  • Data archival
  • GCLP compliance

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Exton, Pennsylvania
Posted
Aug 18, 2026
Application
Employer website
Frontage Laboratories logo

Hiring organization

Frontage Laboratories

Frontage Laboratories is a US-based Contract Research Organization (CRO) that was initially established in New Jersey in April 2001 and later relocated to Pennsylvania in 2004. As an FDA-registered and inspected global pharmaceutical development and manufacturing organization,...

IndustryResearch Services
TypePublic Company
Size1,001-5,000 employees
View profile

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Market context

Pennsylvania Laboratory Applications Roles Favor Scientific Training

Pennsylvania laboratory application specialist roles typically value life sciences graduates who can support laboratory workflows, documentation, and regulated processes. Competition may favor candidates with even limited laboratory or document management experience, particularly in regulated settings, plus clear communication and organizational skills. Review the AI-summarized requirements and benefits here—covering degree, experience, insurance, disability coverage, and 401(k)—to save research time, then tailor your application to relevant documentation experience.

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