Full-Time

Laboratory Investigator

Updated on 9/12/2026

LFB

LFB

1,001-5,000 employees

Public health biopharmaceuticals via plasma-derived products

No salary listed

Les Ulis, France

Hybrid

Telework is available up to two days per week after the probationary period is validated.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Six Sigma
GMP
FDA Regulations

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Requirements
  • A BAC+5 diploma, pharmacist qualification, or engineering qualification in science, process, or process engineering is required.
  • At least five years of professional experience in the pharmaceutical industry is required.
  • Knowledge of regulations such as Good Manufacturing Practices and Food and Drug Administration requirements is required.
  • Knowledge of pharmaceutical processes is required.
  • Knowledge of continuous-improvement tools and processes is required.
  • Knowledge of problem-solving methods is required.
  • Knowledge of risk-analysis methods is required.
  • Experience using software and computer systems is required.
Responsibilities
  • Handle complex critical and major investigations, including those with significant quality or customer-service impact or potential implications for product release, such as deviations, complaints, pharmacovigilance notifications, and other alerts.
  • Analyze deviations, assess their impacts, and determine root causes.
  • Define preventive and corrective actions and CAPA plans for the relevant deviations.
  • Provide methodological and analytical or testing expertise to Control Laboratories teams when needed.
  • Participate in working groups and cross-functional projects.
  • Contribute to the evolution and continuous improvement of the LFB deviation-management system and processes.
  • Report alerts and follow-up activities to the responsible pharmacist.
  • Present investigation conclusions, impact analyses, and proposed action plans to the responsible pharmacist and management during critical-deviation review committees.
  • Present handled deviations to the French National Agency for Medicines Safety when needed as part of the batch-release process.
  • Participate in drafting alert forms and presenting the subject when an alert is made to health authorities.
  • Participate in internal and external audits or inspections and present handled topics to auditors or inspectors.
Desired Qualifications
  • Knowledge of Six Sigma, with Yellow Belt or Green Belt certification or training, is desirable.

LFB is a French biopharmaceutical company that develops and manufactures medicines from plasma and biotech products. It collects plasma, fractionates it into medicines, and also produces recombinant proteins for rare diseases in immunology and hemostasis, sold in many countries. It stands out because it started as a state-initiated public health mission and remains state-owned with the French State as sole shareholder, plus vertical integration through acquisitions of plasma collection firms. Its goal is to ensure a reliable supply of essential medicines for public health while growing as a global biopharma player.

Company Size

1,001-5,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Courcebœufs, France

Founded

1994

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Simplify Jobs

Simplify's Take

What believers are saying

  • Arras released first medicines in 2025, proving commercialization after heavy capital spending.
  • LFB signed a 2026 collaboration with Sartorius to accelerate client programs and GMP manufacturing.
  • France 2030 funding and the 2026 Alès expansion add capacity and roughly fifty jobs.

What critics are saying

  • EFS must raise plasma collections to 1.4 million liters by 2028 or Arras underutilizes.
  • LFB BIOMANUFACTURING still depends on Sartorius for cell line development, limiting full-stack control.
  • A single French industrial base creates existential exposure to contamination, recalls, or regulatory shutdowns.

What makes LFB unique

  • French state-owned sole domestic plasma fractionator anchors national medicine supply.
  • Arras plant, authorized in 2025, centralizes production and triples plasma-derived capacity.
  • Europlasma and Amber Plasma give LFB 24 Central European collection centers.

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Benefits

Health Insurance

401(k) Retirement Plan

Remote Work Options

Unlimited Paid Time Off

Flexible Work Hours

Paid Vacation

Hybrid Work Options

Wellness Program

Mental Health Support

Phone/Internet Stipend

Home Office Stipend

Stock Options

Company Equity

Conference Attendance Budget

Family Planning Benefits

Fertility Treatment Support

Professional Development Budget

Education allowance

Tuition Reimbursement

Growth & Insights and Company News

Headcount

6 month growth

7%

1 year growth

7%

2 year growth

6%
MyPharma Editions
May 30th, 2024
LFB Acquires Amber Plasma in Czech Republic

Title: "LFB Acquires Amber Plasma in the Czech Republic" LFB and its subsidiary Europlasma have acquired Amber Plasma, which operates 12 plasma collection centers in the Czech Republic. This acquisition increases Europlasma's total to 24 centers in Central Europe, enhancing LFB's plasma collection capacity. The move supports LFB's goal to meet growing patient demand and will aid in the launch of a new production site in Arras, France, tripling its medication production capacity.