TScan Therapeutics

Manufacturing Associate II

TScan Therapeutics$95K — $122K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • High School Diploma or GED required; Bachelor's degree preferred.
  • 2-4+ years of experience in cGMP manufacturing in biotech or pharma.
  • Prior cell therapy manufacturing experience highly preferred, advanced biologics experience acceptable.
  • Fluency in reading, writing, and speaking English.
  • Experience in reviewing and creating controlled documents.
  • Ability to lift up to 50 pounds and perform tasks in a compliant manner after safety training.
  • Intermediate skills in Microsoft Office applications.

Responsibilities

  • Execute cGMP manufacturing of TScan cell therapy products while adhering to all relevant guidelines.
  • Complete production documentation for each processing step accurately.
  • Maintain cleanliness and order in the manufacturing area and ensure it is stocked with necessary supplies.
  • Participate in batch record reviews and updates to manufacturing documents.
  • Leverage manufacturing knowledge to suggest process improvements and continuous enhancements.
  • Document all production efforts meticulously in logs and databases.
  • Identify and assist in corrective actions for any processing issues.

Benefits

  • On-site work at a cGMP Manufacturing site in Waltham, MA.
  • Shift schedule including rotating day shifts.
  • Training provided before shift rotation.
  • Opportunities for participating in continuous process improvement initiatives.
Full Job Description
Position Summary:

We are hiring Manufacturing Associate I-II to support and drive our internal Cell Therapy Manufacturing. These positions will be based in our cGMP Manufacturing site in Waltham, MA.

The ideal candidates have demonstrated experience in cell therapy or biologics manufacturing, have robust knowledge of cGMPs, and enjoy fast-paced, collaborative environments. A team player with a sense of urgency will thrive in this role.

This role is on-site and will follow a shift schedule. Roles will train on a Monday - Friday schedule before transitioning to rotating day shifts (including weekends) for operations.

Responsibilities:

Responsibilities include, but are not limited to:
  • Execute cGMP manufacturing of TScan cell therapy products while adhering to cGMPs, SOPs, compliance/regulatory mandates, safety procedures, and quality requirement
  • Accurately complete appropriate production documentation for all processing steps
  • Maintain cleanliness and orderliness of process area, ensuring production area is stocked with supplies
  • Participate in batch record review, procedure revisions, and bill of materials
  • Utilize manufacturing knowledge to improve process operations and assist in the identification and implementation of continuous improvement opportunities
  • Assist in the creation and revision of manufacturing documentation
  • Maintain equipment operation through responsive troubleshooting, repairs, and following operation guidelines
  • Document all production efforts in appropriate logs, forms, reports, and databases
  • Identify and assist in the corrective actions of processing-related issues

Requirements:
  • High School Diploma or GED required, at minimum; Bachelor's degree preferred
  • 2-4+ years of experience in cGMP manufacturing in the biotech or pharmaceutical industry
    • Prior cell therapy manufacturing experience highly preferred, advanced biologics required in lieu of CT
  • Must be able to read, write, and speak English fluently
  • Experience in reviewing and creating controlled documents
  • After safety training, must be able to perform required tasks in a fully compliant manner
  • Must be able to lift and transport (using carts or wheelies) packages weighing up to 50 pounds
  • Extensive walking throughout the facility will be required
  • Demonstrated success in delivery of key milestones against tight timelines
  • Ability to prioritize, manage time well, multitask, troubleshoot
  • 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: $95,000 - $122,500

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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