Assurance Specialist #26-26140

Us Tech Solutions

Collegeville (PA)

On-site

USD 65,000 - 85,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

US Tech Solutions is seeking a detail-oriented quality documentation professional for an 11-month contract in Collegeville, PA. You will manage controlled document lifecycles, coordinate reviews, and ensure audit-ready records within a regulated tech or life sciences environment.

Responsibilities include end-to-end documentation, stakeholder coordination, and strict adherence to quality processes, with exposure to GAMP 5, 21 CFR Part 11, and SDLC concepts.

Qualifications

  • 3-5 years of experience managing controlled document lifecycles in regulated tech or life sciences.
  • Familiar with GAMP 5 and 21 CFR Part 11 concepts.
  • Strong technical writing with audit-ready records.
  • Experience with QMS/eQMS or document management systems and version control.
  • Proficient in coordinating reviews, approvals and sign-offs with stakeholders.
  • Knowledge of SDLC in Agile/ Scrum or Waterfall environments.
  • Awareness of cloud/security principles and data classification.
  • Experience in pharma or life sciences regulatory contexts.
  • Proficient with Jira and Confluence tooling.
  • Understanding of IQ/OQ/PQ concepts beneficial.

Responsibilities

  • Assist in end-to-end documentation lifecycle management for engineering, ensuring artifacts are produced, reviewed, approved and retained.
  • Liaise with contributors to progress drafts, coordinate reviews and secure approvals.
  • Support documentation reviews from a technical writing perspective and flag issues.
  • Maintain repositories and version control for audit readiness and traceability.
  • Support adherence to risk/issue management policies and report status to the Quality team.
  • Manage routing and finalization of documents, including uploading and sign-offs.

Skills

Document lifecycle
Version control
Technical writing
Stakeholder follow-up
Risk & issue tracking
Quality partner collaboration
SDLC exposure
Information security awareness
Regulated industry experience
Jira & Confluence
Validation/GRC concepts

Education

Bachelor's Degree in a Scientific Discipline

Tools

Confluence
SharePoint

Job description

Duration: 11 Months Contract

Schedule: 08:00 AM - 5:30 PM

Job Description
  • Detail-oriented quality documentation professional with 3-5 years of experience managing controlled document lifecycles in a regulated technology or life sciences environment. Skilled in document review, version control, stakeholder follow-up and tracking of risks, issues and CAPAs through to closure. Working knowledge of the SDLC and computerised systems validation concepts (GAMP 5, 21 CFR Part 11), with awareness of information and cloud security principles. Strong technical writing background, supporting senior quality colleagues in maintaining audit-ready, traceable records.
Responsibilities
  • In coordination with the assigned Quality team member, assist in managing the end-to-end documentation lifecycle for engineering, ensuring that required artifacts are produced, reviewed, approved and retained in accordance with applicable quality processes, and report progress or issues as needed for final review.
  • Proactively liaise with contributors and stakeholders, in consultation with the assigned Quality team member, to progress draft documentation, coordinate reviews and secure requisite approvals.
  • Provide support in documentation review from a technical writing perspective and flag suspected issues, collaborating with the assigned Quality team member where necessary.
  • Maintain documentation repositories and version control practices to preserve audit readiness and traceability, keeping the assigned Quality team member informed of repository status and any version-control concerns.
  • Support adherence to internal policies governing risk and issue management, including follow-up of outstanding or overdue records as assigned by the Quality team, and provide status updates to the assigned Quality team member.
  • Manage document routing and administrative finalization (uploading, version tracking, coordinating sign-offs), in consultation with the assigned Quality team member.
Experience
  • 3-5 years of experience.
Skillsets
  • Document lifecycle: Hands-on experience routing documents through draft, review, approval and retention in a controlled environment (QMS, eQMS or document management system).
  • Version control and repositories: Experience maintaining repositories (such as SharePoint, Confluence or a validated DMS) with traceability and audit readiness.
  • Technical writing and editing: Proofreading, formatting and reviewing technical documents for clarity and consistency, and flagging suspected issues. A writing, English, communications or similar degree, or equivalent demonstrated experience, fits well.
  • Stakeholder follow-up: A record of chasing contributors, reviewers and approvers to meet deadlines, escalating appropriately to a quality lead.
  • Risk and issue record upkeep: Experience tracking deviations, CAPAs, incidents, risks or issues to closure, including overdue items, and providing status updates.
  • Working with a quality partner: Comfortable supporting a more senior quality person, reporting progress and raising issues rather than owning decisions.
  • SDLC exposure: Has worked within or alongside a software development lifecycle (Agile, Scrum or waterfall), for example by producing or managing documentation artifacts such as requirements, specifications, test records or release summaries.
  • Information/cloud security awareness: Understands principles such as access control, data classification, confidentiality and shared responsibility in cloud environments. Certification is not required.
  • Experience in a regulated industry (pharma, life sciences or similar) with 21 CFR Part 11 or Annex 11 familiarity
  • Jira and Confluence, or comparable tools
  • Validation/GRC concepts: Understands the basics of computerized systems validation, qualification and risk-based approaches, ideally GAMP 5 and the idea of a validated state. Hands-on authoring of IQ/OQ/PQ is not required.
Education
  • Bachelor's Degree in a Scientific Discipline.
About US Tech Solutions

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com .

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

AI Statement: By applying, you acknowledge that AI‑assisted tools may be used during hiring.

IND01

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Compliance Specialist - Level 2 US_AGS
Compliance Specialist - Level 2 US_AGS

Lancesoft • Collegeville (PA)

Hybrid
USD 65,000 - 90,000
Document Control Assistant
Document Control Assistant

Kelly Services • Salt Lake City (UT)

On-site
USD 30,000 - 42,000
Quality Assurance Senior Associate #26-27458
Quality Assurance Senior Associate #26-27458

US Tech Solutions • Holly Springs (NC)

On-site
USD 90,000 - 130,000
Document Control Assistant
Document Control Assistant

Kelly • Salt Lake City (UT)

On-site
USD 30,000 - 41,000
Technical Writer # 26-25662
Technical Writer # 26-25662

Us Tech Solutions • Fort Washington

On-site
USD 60,000 - 85,000
Quality Specialist - Remote Opportunity
Quality Specialist - Remote Opportunity

Dayton T. Brown Inc. • United States

Remote
USD 70,000 - 95,000
Tuition reimbursement
Profit sharing
401K with company match
+2
Quality Documentation & Technical Writer
Quality Documentation & Technical Writer

Efficient Auditing • Atlanta (GA)

On-site
USD 70,000 - 90,000
QA Documentation Specialist I
QA Documentation Specialist I

TekWissen LLC • Vacaville (CA)

On-site
USD 27,552 - 34,440
Senior Document Control Specialist
Senior Document Control Specialist

Select Source International • California

On-site
USD 40,000 - 54,000
Quality Specialist
Quality Specialist

Infotree Global Solutions • Salt Lake City (UT)

On-site
USD 30,000 - 39,000