Analytical Validation Engineer

Piper Companies; Titusville (NJ); On-site; USD 80,000 - 100,000; Full time

Job summary

An innovative firm is on the lookout for an Analytical Validation Engineer to support critical commissioning and decommissioning activities for a leading pharmaceutical company. This role requires expertise in laboratory operations and a solid background in GMP environments. You will engage in various responsibilities, including instrument qualification and laboratory investigations, while collaborating with a dynamic team. If you thrive in a fast-paced environment and possess strong analytical and problem-solving skills, this is an exciting opportunity to make a significant impact in the pharmaceutical sector.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401K

Paid Time Off

Sick Leave

Holidays

Qualifications

• 5+ years of experience in a GMP environment is required.
• Strong interpersonal skills and ability to manage multiple tasks.

Responsibilities

• Support laboratory investigations from initiation to conclusion.
• Hands-on experience with GMP laboratory instruments.

Skills

Pharmaceutical Laboratory Operations

Root Cause Analysis

Analytical Skills

Problem-Solving

Education

Bachelor’s Degree in Chemistry

Bachelor’s Degree in Biology

Bachelor’s Degree in Biochemistry

Tools

HPLC (Waters)

AA

NIR

ICP

FT-IR

Gas Analyzers

Particle Counters

Job description

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Job Overview

Piper Companies is seeking an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Titusville, NJ area.

Responsibilities

1. Experience in Pharmaceutical Laboratory Operations.
2. Familiarity with laboratory instrument selection, installation (IQ/OQ), and qualification (PQ).
3. Support for laboratory investigations from initiation to conclusion, including root cause analysis, CAPA implementation, and final report writing.
4. Hands-on experience with GMP laboratory instruments (e.g., AA, HPLC (Waters), Autotitrators, NIR, ICP, FT-IR, particle counters, Gas analyzers).

Qualifications

1. Bachelor’s Degree in Chemistry, Biology, or Biochemistry with at least 5 years of GMP environment experience.
2. Ability to manage multiple projects/tasks independently.
3. Strong interpersonal skills, including flexibility, collaboration, and teamwork.
4. Self-starter with innovative problem-solving capabilities.
5. Analytical skills, critical thinking, and application of key concepts.

Compensation

1. Salary Range: $55 - $60/hr.
2. Benefits include Medical, Dental, Vision, 401K, PTO, Sick Leave, and Holidays.

Additional Information

Applications open on 02/12/2025 and will be accepted for at least 30 days.

Job Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Quality Assurance
• Industries: Business Consulting and Services