Genezen

Process Engineer I

BS in Chemical or Mechanical Engineering; 0-3 years experience; strong written and spoken communication; multi-tasking; on-call; pharma equipment experience; cell culture/protein purification desirable.

Associate, Quality Operations

Bachelor’s degree in science; 3-5 years QA experience in pharma/biologics; knowledge of cGxPs, clean rooms; experience with early phase clinical trial production; strong cross-functional collaboration.

Director of Business Development

5+ years sales/technical or client relationship experience; CRM; biology/biotech background; strong negotiation; experience in regulated environments.

Stability Manager, Quality Control 

Stability Manager

8+ years CDMO experience; leadership of stability programs; GMP knowledge; experience with deviations, CAPAs, change controls; analytical method familiarity.

QC Analyst - Bioassay Temp - 2nd Shift (1-9:30pm)

QC Analyst

BA/BS in Biochemistry/Cell Biology; 2+ years lab QC experience; cell culture and cell-based assays; MS Word, Excel, LIMS; good communication and organization.

Automation Engineer I/II/III

Automation Engineer

Bachelor's in engineering or computer science; 2-8+ years; PLC/SCADA; cGMP/21 CFR Part 11; pharma equipment commissioning; on-call; Lexington, MA.

Manufacturing Supervisor - 1st Shift

Manufacturing Supervisor

Lead GMP manufacturing operations; ensure safety, cGMP compliance, and scheduling; supervise upstream/downstream and cell/virus banking teams.

Manufacturing Technician I/II/III (2nd Shift)

Manufacturing Technician

2-4 years cGMP manufacturing experience; high school diploma required; degree in Life Sciences/Engineering preferred.

Manufacturing Supervisor - 2nd Shift (2:00-10:30pm)

3-5+ years of cGMP manufacturing leadership; Bachelor's in Life Sciences/Engineering; strong documentation and scheduling skills; GMP audits readiness.

Validation Engineer II/III (CSV)

Validation Engineer

5+ years validation experience; BS in Engineering; GMP knowledge; strong communication; familiarity with regulatory standards (21 CFR Part 11, ICH Q7A, GAMP 5).

Lead, QCTS Data Integrity & Computerized Systems

Lead for QC data integrity and computerized systems; 10+ years GMP/CSV/IT experience; expertise in 21 CFR Part 11, EU Annex 11; GDP; Excel; data governance; strong communication.

Sr/Principal Scientist - Upstream Process Development

Upstream Process Development Scientist

Senior scientist with MSc/PhD in bioprocess engineering or life sciences; 8+ years (MSc) or 6+ years (PhD) experience in upstream development, tech transfer, GMP manufacturing, and cross-functional collaboration.

Validation Technician I/II

Validation Technician

1+ years in a regulated (cGMP) environment; AS degree or certificate in science/tech; strong communication; calibration experience.

Specialist I/II/III, Calibration

Calibration Specialist

3-5 years calibration/metrology experience; associates and bachelor degrees; CMMS experience; strong communication and mechanical skills.

Sr. Program Manager

Program Manager

Senior Program Manager with 5+ years pharma/biotech project management; BS in life sciences or related field; PMP preferred; strong communication; MS Project experience; 3+ years life science lab experience desired.

Title	Location	Date
Process Engineer I Full Time · $65K-$85K · 0+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Apr 14, 2026
Associate, Quality Operations Full Time · 3+ YOE Fishers or Indianapolis or Lexington · Onsite	Fishers or Indianapolis or Lexington Onsite	Apr 8, 2026
Director of Business Development Full Time · $165K-$185K · 5+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Apr 6, 2026
Stability Manager, Quality Control Full Time · $130K-$150K · 8+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Apr 6, 2026
QC Analyst - Bioassay Temp - 2nd Shift (1-9:30pm) Temporary · 2+ YOE Lexington, Massachusetts, United States · Onsite	Lexington, Massachusetts, United States Onsite	Mar 31, 2026
Automation Engineer I/II/III Full Time · $65K-$130K · 2+ YOE Lexington, Massachusetts, United States · Onsite	Lexington, Massachusetts, United States Onsite	Mar 28, 2026
Manufacturing Supervisor - 1st Shift Full Time · 5+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Mar 27, 2026
Manufacturing Technician I/II/III (2nd Shift) Full Time · 2+ YOE Lexington, Massachusetts, United States · Onsite	Lexington, Massachusetts, United States Onsite	Mar 25, 2026
Manufacturing Supervisor - 2nd Shift (2:00-10:30pm) Full Time · 3+ YOE Lexington, Massachusetts, United States · Onsite	Lexington, Massachusetts, United States Onsite	Mar 20, 2026
Validation Engineer II/III (CSV) Full Time · $90K-$130K · 5+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Mar 19, 2026
Lead, QCTS Data Integrity & Computerized Systems Full Time · $110K-$150K · 10+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Mar 19, 2026
Sr/Principal Scientist - Upstream Process Development Full Time · $120K-$170K · 8+ YOE Lexington, Massachusetts, United States · Onsite	Lexington, Massachusetts, United States Onsite	Mar 12, 2026
Validation Technician I/II Full Time · $56K-$79K/yr · 1+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Mar 6, 2026
Specialist I/II/III, Calibration Full Time · 3+ YOE Fishers or Lexington · Onsite	Fishers or Lexington Onsite	Jan 30, 2026
Sr. Program Manager Full Time · 5+ YOE Lexington or Fishers · Onsite	Lexington or Fishers Onsite	Sep 12, 2025

Activities	Viral vector manufacturingProcess developmentCell transduction servicesAnalytical testing servicesGMP production
Headquarters	US
Industries	BiotechnologyPharmaceuticals
Name	Genezen
Employees	217
Type	Private
Tagline	Produces viral vectors for cell and gene therapy programs.
Founded	2,014
Website	genezen.com
Latest Funding Round	Private Equity
Latest Funding Year	2,023
Latest Funding Amount	18,500,000
Latest Investors	Ampersand Capital Partners

Genezen

About Genezen