Workforce Genetics

60 Workforce Genetics Jobs Hiring Near You

CSV Engineer (6mo. Contract-to-Hire) Location: Baltimore, MD Company Join a premier global Contract Development and Manufacturing Organization (CDMO) that is rapidly expanding its state-of-the-art ...

About LifeSprout LifeSprout was founded in September 2015 as a Johns Hopkins University spinout. We are a medical device company creating revolutionary products for aesthetic and reconstructive ...

The geneticist clinician will provide inpatient consultation to pediatric and adult patients ... We believe in creating a talented, engaged, and driven workforce through on-going development and ...

Workforce Manager

$65K - $75K/yr

The Workforce Manager is responsible for supporting workforce management systems, forecasting ... genetic information, pregnancy, marital status, sex, gender, gender identity, gender expression ...

New

Analyze various workforce management data points for accuracy. ESSENTIAL JOB FUNCTIONS Gather and ... genetic information (including testing or characteristics) or another protected status as defined ...

Analyze various workforce management data points for accuracy. ESSENTIAL JOB FUNCTIONS Gather and ... genetic information (including testing or characteristics) or another protected status as defined ...

Job Summary: We are seeking a proactive Workforce Supervisor to lead and support our production ... genetic information, or any other status protected by law. Surge is committed to providing access ...

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Workforce Genetics Jobs Information

Infographic showing various job openings at Workforce Genetics in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% Physical job distribution.

Quality Remediation Project Lead

Workforce Genetics

Baltimore, MD

$70 - $100/hr

Full-time

Posted 18 hours ago

Posted today


Job description

Workforce Genetics is assembling a high-impact, 5-person contingent quality team to support a premier pharmaceutical manufacturing facility in the Greater Baltimore Area. The site is executing an intensive quality remediation project to address an active backlog of open investigations, deviations, and CAPAs. The primary immediate objective is an aggressive clearance of high-priority deviations.


We are actively recruiting 1 Project Lead for this dedicated, 6+ month on-site project.


Responsibilities:

  • Scope: Serves as a hands-on manager and project lead who tracks daily completion metrics, identifies systemic workflow blockers, updates operational leadership, and coordinates directly with global QA teams while actively assisting in writing deviations.


General Candidate Profile & Technical Requirements

  • Experience: Minimum 5–6 years within biopharma/GMP compliance environments, specifically showing history managing quality, compliance or manufacturing writing teams, efficient and high quality project delivery.
  • Core Competency:
  • Proven expertise in systematic root-cause analysis (RCA) methodologies and standard cGMP technical writing.
  • Strong preference for professionals with eclectic experience across upstream processing, downstream processing, and fill lines. Familiarity with Oral Solid Dose (OSD) manufacturing and visual inspection processes is a significant advantage.
  • A formal academic degree is not strictly required; technical mastery, an ability to write cleanly under tight compliance timelines, and a strong history on the manufacturing floor are the primary drivers for selection.


Core Hours: Mon–Fri, 8AM–5PM (Standard Business Hours)