1737- Content Quality Specialist

About the role

LogicSource is an innovative leader in sourcing and procurement services, helping companies increase profits through better buying. Operated by a 500‑person collective of procurement professionals, we are deeply rooted in data and insight‑driven strategic sourcing, category management, operational excellence, and value delivery. Partnering with Fortune 500 companies, we build and nurture strategic relationships while delivering strong execution that drives measurable bottom‑line impact and the development of best‑in‑class procurement capabilities. Learn more about us at www.logicsource.com.

A collaborative, supportive culture where your contributions are valued, and your work makes a meaningful impact. A workplace committed to professional growth with paths to development and advancement. Dedicated to creating an environment for employee success by providing support for long‑term career growth. Committed to work‑life balance by offering flexible PTO. A robust benefits package that includes extensive health, dental, and vision coverage for you and your family. Employer‑funded HRA, a 401(k) match, Healthcare and Dependent Care FSAs, short‑ and long‑term disability coverage, AD&D, life insurance, fertility assistance, and more. Supplemental benefits such as unexpected large expenses related to Accidents, Hospitalization, or Critical Care. Along with support for Maternity/Paternity, FMLA, and Military leave. Offer behavioral health services within the medical support insurance plan and everyday support tools to help with mental health. A business‑casual workplace offering a flexible, hybrid work environment with offices in Westport, CT, and Charleston, SC.

We have an immediate opening for a full‑time Content Quality Specialist (CQS) on one of our client teams. This is a 12‑month contract role. The CQS will regularly engage with stakeholders in marketing, operations, legal, regulatory, medical, and ad agencies. The CQS will document and confirm accuracy of content corrections and alignment across all channels to maximize on‑time review and approval for promotional materials. Scope of work is across all US Business Units (Respiratory, Immunology, Oncology, Vaccines, Infectious Disease, & ViiV), including print and digital materials. The CQS will consult with marketing content owners and negotiate with promotional review team members to resolve content barriers and ensure timely completion of post‑approval content updates.

Responsibilities

• Exhibits traditional editorial/proofreading skills.
• Edit advertising, promotional, and educational projects to ensure:
  • a) accuracy of spelling, grammar, punctuation, syntax, and context;
  • b) accuracy of references and other data;
  • c) compliance with GSK corporate, American Medical Association (AMA), and FDA guidelines;
  • d) correct usage and presentation of GSK trademarks, logos, and corporate branding;
  • e) consistency and accuracy of layout components;
  • f) overall sense, continuity, consistency, and clarity: standardized, industry‑specific editorial practices and methodologies ensure highest‑quality printed, online, and digital content.
• Assumes the risks and responsibilities required of the role as the key contact for changes to regulated GSK promotional content, including mediation and collaboration with team members. The CQS opens meetings, reviews agenda, and maintains team focus on review/comment resolution.
• Increases speed to market and reduces corrections