SonicJobs Logo
Left arrow iconBack to search

GLP QA Specialist II

Celldex Therapeutics
Posted 2 months ago, valid for 12 days
Location

Fall River, MA, US

Salary

$87,831 - $114,066 per year

Contract type

Full Time

Health Insurance

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • This role involves maintaining quality systems, tracking QA metrics, and ensuring adherence to FDA GLP requirements while collaborating with cross-functional teams.
  • The ideal candidate should have a Bachelor’s degree in Life Sciences and 1-3 years of QA experience in the Biotech or Pharma industry.
  • Key responsibilities include managing GLP document control systems, laboratory notebooks, and executing GLP QA systems.
  • The expected base salary for this position ranges from $76,374 to $99,189, depending on various factors including experience and education.
  • Celldex is an equal opportunity employer committed to diversity, equity, and inclusion in its workplace.

Overview

This role is responsible for maintaining quality systems, tracking and reporting QA metrics, managing laboratory documentation processes, and ensuring adherence to FDA GLP requirements while partnering with cross-functional teams to drive continuous improvement and quality excellence. The ideal candidate is detail-oriented, highly organized, and capable of working independently and collaboratively to support the integrity, accuracy, and compliance of quality operations across the organization.

 

Responsibilities

  • Maintain GLP document control system including preparing, updating, formatting, distributing, issuing, and tracking GXP documents
  • Manage, distribution, and reconciliation of laboratory notebooks
  • Manage GLP QA periodic reports
  • Assist in GLP QA systems execution supporting GLP testing
  • Create, trend, and report GLP QA Quality Systems information
  • Perform internal GLP audits

Qualifications

  • Bachelor Science (BS)/Bachelor Arts (BA) degree in Life Sciences preferable.

  • 1-3 years QA experience in Biotech/Pharma industry.

  • Strong working knowledge of EDMS (electronic document management system)

  • Strong working knowledge of cGMP/GLP.

  • Strong working knowledge of MS Word,  Excel and related databases
  • The ability to work independently and as part of a team
  • Excellent communication skills.

 

 

CompensationThe expected base salary range for this position is $76,374 to $99,189

We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.

Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.

Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach




Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.