Parexel Scientist II or III (Metrology Specialist) Recruitment 2026: Apply Online for Various Vacancies
Scientist II or III – Metrology Specialist – FSP
Job Overview
Parexel International is currently seeking a highly skilled and motivated professional to fill the position of Scientist II or III – Metrology Specialist – FSP. This is a full-time, long-term assignment onsite at one of our premier client locations in Rahway, New Jersey. As a Metrology Specialist under the Functional Service Provider (FSP) model, you will be integrated directly into the client’s operations, combining the stability and benefits of working for a world-class Clinical Research Organization (CRO) with the dynamic exposure of a top-tier pharmaceutical sponsor environment.
Role Overview and Core Mission
The Metrology Specialist plays a critical role in ensuring the integrity, compliance, and operational readiness of both regulated and non-regulated laboratory equipment. In a highly regulated pharmaceutical development environment, the accuracy of analytical instruments is paramount. This role oversees the entire lifecycle of laboratory instrumentation, which spans from the initial acquisition and installation to routine maintenance, computer system validation (CSV), and eventual retirement of regulated systems. By maintaining these systems to the highest standards, you directly support the discovery and development of novel, life-saving therapies.
Key Lifecycle Responsibilities
Your daily activities will involve a blend of hands-on technical troubleshooting, documentation management, and cross-functional collaboration. Key responsibilities include:
- Documentation & Compliance: Preparing, reviewing, and approving critical instrument documentation, including master equipment lists, qualification protocols, and calibration records to ensure audit readiness.
- Vendor Management: Coordinating service activities with external vendors and service engineers, building strong relationships to ensure minimal downtime for critical laboratory assets.
- Technical Troubleshooting: Developing a deep working knowledge of complex laboratory equipment to perform routine maintenance, calibration, and rapid troubleshooting.
- Computer System Validation (CSV): Participating in validation activities for standalone computer systems and software upgrades associated with laboratory instrumentation.
- Quality Assurance: Originating and progressing Notice of Event (NOE) and Change Management (CM) records, performing thorough investigations, and implementing Corrective and Preventive Action (CAPA) plans.
Why Join Parexel FSP?
Parexel FSP offers a unique career path where you can grow your skills in a supportive, collaborative, and inclusive community. We prioritize putting people first, allowing you to achieve your best work. This position offers a comprehensive benefits package, including:
- Full medical, dental, and vision benefits.
- Generous paid time off (PTO) and sick time.
- 401(k) retirement plan with company match.
- Paid holidays and continuous professional development opportunities.
- A work culture that keeps patients at the center of everything we do.
Please note that this position is located onsite in Rahway, NJ, and does not offer visa sponsorship. Candidates must be fully authorized to work in the United States.
About Parexel’s CMC Operations
The CMC (Chemistry, Manufacturing, and Controls) Operations group within Parexel FSP is dedicated to providing pharmaceutical and biopharmaceutical companies with top-tier technical professionals. Our team supports the critical phases of drug discovery, formulation, and analytical development. By joining this group, you become part of a global network of scientists and engineers who are passionate about advancing healthcare. We foster an environment of continuous learning, where you can leverage cutting-edge technologies, participate in process improvement initiatives, and collaborate across multiple testing labs and sites to drive operational excellence.
Key Job Details
| Company Name | Parexel |
| Job Role | Scientist II or III – Metrology Specialist – FSP |
| Experience | Scientist II: B.S. with 1-2 years or M.S. with 0-1 years. Scientist III: B.S. with 3-5 years or M.S. with 1-2 years. |
| Salary Range | Competitive Industry Standards (Full Benefits, 401K, PTO) |
| Job Type | Full-Time |
| Work Mode | Onsite |
| Openings | Various |
| Job Location | Rahway, New Jersey, United States |
Key Responsibilities
- Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation.
- Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships.
- Gain a working knowledge of laboratory equipment to facilitate troubleshooting and/or perform maintenance or calibration activities.
- Participate in computer system validation activities associated with new or upgraded equipment or software packages.
- Support the purchase, installation, and equipment qualification of new laboratory equipment.
- Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training, and cross-site support.
- Originate and progress Notice of Event (NOE) and Change Management (CM) records.
- Perform and document investigations and assist in developing/implementing CAPA plans.
- Represent the laboratory on all aspects of laboratory equipment during audits.
- Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures.
Requirements & Qualifications
- B.S. or M.S. in Chemistry, Biochemistry, Engineering, or a related discipline.
- Experience working within a regulated (GMP) laboratory environment.
- Hands-on experience maintaining, operating, and troubleshooting laboratory equipment (HPLC, GC, UV-Vis, etc.).
- Familiarity with standalone computer system GMP validation requirements.
- Highly organized and capable of multitasking to manage laboratory equipment schedules and documents.
- Capable of working independently under moderate supervision.
- Strong verbal, written, and interpersonal communication skills.
- Familiarity with authoring relevant instrument standard operating procedures (SOPs).
- No sponsorship provided; must have valid US work authorization.
Required Skills
- High-Performance Liquid Chromatography (HPLC)
- Gas Chromatography (GC)
- Ultraviolet-Visible Spectroscopy (UV-Vis)
- Dissolution Systems
- Computer System Validation (CSV)
- GMP Compliance & cGMP Regulations
- Standard Operating Procedures (SOP) Authoring
- Vendor Coordination & Relationship Management
- Notice of Event (NOE) & Change Management (CM)
- CAPA (Corrective and Preventive Actions) Planning
About Parexel
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
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