TScan Therapeutics

Manager, Quality Systems

TScan Therapeutics$130K — $150K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • MS with 10-12 years or BS with 12-15+ years of experience in an FDA-regulated industry; high school diploma or GED required at minimum.
  • Minimum of 8 years in quality compliance.
  • Experience with Veeva DMS, QMS or similar electronic systems preferred.
  • ASQ Quality Auditor and/or Manager of Quality Certification is a plus.
  • Proficient in reading, writing, and speaking English fluently.
  • Strong documentation and communication skills are essential.
  • Excellent technical writing skills are a plus.

Responsibilities

  • Manage TScan's Vendor Management Program, ensuring GxP vendor qualification.
  • Conduct external audits and oversee pre and post audit activities.
  • Assist in executing TScan's Internal Audit program, including internal audits and related activities.
  • Support Deviation, CAPA, and Change Control programs as needed.
  • Oversee other Quality Management Systems such as Training Management and Document Control programs.
  • Author or revise controlled documents linked to quality systems.
  • Monitor and reconcile controlled documents for GMP manufacturing environments.

Benefits

  • Collaborative and vibrant startup culture.
  • Opportunities for continuous improvement.
  • Potential annual bonus and equity awards.
  • Commitment to adherence to safety procedures and guidelines.
Full Job Description
We are looking for an experienced Quality Assurance professional to join our team as Manager, Quality Systems supporting our novel target identification and validation workflow in house. The ideal candidate should have relevant experience in quality compliance, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role.

Responsibilities:
  • Own and Manage TScan's Vendor Management Program and ensure all GxP vendors are qualified as per approved procedures.
  • Perform external (Vendor) audits and lead pre and post audit activities.
  • Assist in TScan's Internal Audit program. Perform internal audits as required and assist in pre and post audit activities.
  • Assist in managing Deviation, CAPA, Change Control programs as needed.
  • Assist in other Quality Management Systems including but not limited to Training Management and Doc Control programs.
  • Author or revise applicable controlled documents related to quality systems.
  • Generate, Issue and reconcile controlled documents for the GMP manufacturing environment
  • Assists in the identification and implementation of continuous improvement opportunities.
  • Adhere to all cGMPs, compliance/regulatory mandates and quality requirements.
  • Practice safe work habits and adhere to TScan's safety procedures and guidelines.
  • Perform other related duties as assigned to meet departmental and Company objectives.

Requirements:
  • MS with 10-12 yrs /BS and 12-15+ years of experience, minimum of 8 in an FDA-regulated industry; high school diploma or GED required at minimum
  • Experience with Veeva DMS, QMS or other electronic systems is plus.
  • ASQ Quality Auditor and/or Manager of Quality Certification is plus.
  • Must be able to read, write and speak English fluently.
  • Experience in reviewing and creating controlled documents.
  • Must possess strong documentation and communication skills.
  • Excellent technical writing skills a plus
  • Effectively demonstrates understanding of GxPs and Quality Systems and how they apply to specific responsibilities.
  • Must be able to use a company-issued computer and have at least intermediate skills in Microsoft Word, Excel, Outlook, and PowerPoint programs needed to perform job.

Pay Range: $130,000-$150,000

Pay Transparency

TScan Therapeutics' pay ranges are established based on external market data from third-party compensation surveys and our internal benchmarking. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Individual compensation within this range is commensurate with a candidate's specific qualifications, including education, overall experience, relevant experience, and specific skills. We strive to ensure that compensation is competitive, equitable, and aligned with the value each TScanner brings to the role.

Recruitment & Staffing Agencies

TScan Therapeutics does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics' internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of TScan Therapeutics, and TScan Therapeutics will not owe any referral or other fees with respect thereto.

About TScan Therapeutics

TScan Therapeutics is a biotechnology company that develops T-cell receptor therapies for the treatment of cancer. The company's platform uses a proprietary technology to identify and target cancer cells with high specificity. TScan's lead product candidate, TSC-100, is currently in Phase 1 clinical trials for the treatment of solid tumors. The company was founded in 2018 and is headquartered in Cambridge, Massachusetts.
Learn more about TScan Therapeutics
Size
50 employees
Market Cap
$37.5 million
Industry
NASDAQ

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