Technical Reviewer

Colorado Psychiatric; Longmont, Northern (CO, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Cambrex in Longmont, CO is seeking a Technical Reviewer to independently review analytical data across small and large molecule development, ensuring compliance with cGMP/cGLP and FDA/EU regulations. The role involves evaluating protocols, reports, and laboratory investigations within a fast-paced environment.

You will collaborate with cross-functional teams, manage documentation reviews for project timelines, and support quality systems with strong technical writing and QA principles.

Qualifications

• BA/BS in Life sciences field is required.
• 4+ years of relevant experience in a CDMO/pharma environment.
• Experience in laboratory testing in pharmaceutical/biotechnology industries.
• Strong knowledge of regulatory requirements (FDA, EU, ICH) and GLP/GMP expectations.

Responsibilities

• Perform independent technical review of analytical data and documentation.
• Evaluate protocols and technical reports for qualification/validation and stability.
• Coordinate with analysts and management to document investigations.
• Ensure data meets regulatory requirements and internal procedures.
• Escalate issues that may impact timelines to QA and laboratory management.
• Contribute to department meetings and cross-functional improvements.
• Maintain and advocate for compliant procedures per FDA, EU, and ICH standards.

Skills

Attention to detail

Analytical mindset

FDA/ICH/GMP knowledge

Quality assurance

Technical writing

Education

BA/BS Life sciences

Tools

LIMS/Empower

MasterControl/TrackWise

Microsoft Office

Job description

Cambrex

Technical Reviewer

US-CO-Longmont

Job ID: 2026-4996

Type: Regular Full-Time

# of Openings: 1

Category: Quality Assurance

Cambrex - Longmont

Overview

The Technical Reviewer will work independently to provide a technical review for small and large molecule development and testing data in compliance with cGMP/cGLP standards and FDA / EU regulations. This position specializes in various aspects of technical data and documentation evaluation and review, laboratory investigations, and a variety of routine and non-routine laboratory tasks.

This role will coordinate with appropriate departments and/or cross-functional teams to ensure all applicable documents are reviewed within the specified timeframes. Ability to work within a dynamic and fast paced environment.

Responsibilities

• Responsible for performing an independent technical review of all analytical (small and large molecule entities) GxP testing performed on starting materials, raw materials, intermediates, drug substance, drug product, packaging components, customer samples, stability study samples, in-process testing/checks, etc. for completeness, accuracy and compliance
• Good understanding of analytical laboratory practices and able to apply quality assurance principles to the review process to ensure data is scientifically sound and compliant with all regulatory body requirements and local procedures
• Reviews technical documents such as protocols and technical reports for qualification/validation and stability activities, as required
• Works with analyst and laboratory management to conduct and document laboratory investigations
• Provides accurate and timely delivery of data review and report any findings to the appropriate departments to support overall project due dates
• Escalates issues which may impact timeline to laboratory and quality management
• Ensures all issues/documentation is complete prior to approval
• Participates in department/client meetings, collaborates, and cooperates to achieve cross-functional improvements and business goals
• Good interpersonal skills and willing to ask questions about procedures and concepts
• Participates in the development, implementation, and maintenance of procedures and policies to comply with FDA, EU, and ICH requirements applicable to site's needs
• Able to be trained
• Effectively resolves quality issues and concerns in a timely manner
• Effectively coordinates and organizes tasks to help drive the activities of others; while performing a variety of duties on schedule, with accuracy and competency
• Creates strong and effective working relationships with Quality team, colleagues, and clients

Qualifications / Skills

Knowledge:

• Attention to detail, as well as time and resource management
• Personal and professional integrity and trustworthiness with strong work ethics and the ability to independently with minimal direction
• Promotes a safe environment for work
• Communicates clearly and effectively both orally and in writing with internal and external clients
• Strong knowledge and understanding of LIMS and Empower
• Skilled in MasterControl, Trackwise and/or other QMS software applications, preferred
• Strong knowledge and experience with a wide variety of analytical techniques such as ICP-MS, Patricle Size, XRD, DSC/TGA, NMR. Additional preferred techniques: HPLC, GC, FT-IR, ICP, NIR, UV/Vis, Karl Fischer, Total Particle Counters, required.
• Good understanding and providing effective evaluation of laboratory practices such as raw material, drug substance, drug product and medical device testing, compendia methods (e.g. USP/NF, EP, JP), and method validation/qualification/transfer, as required
• Understanding of microbes (e.g., bacteria, viruses, and fungi) and molecular assays, preferred
• Knowledge of Environmental Monitoring (Air Viable, Total Air Particulate, Surface Viable), Clean Utility Monitoring (Water Sampling, Bioburden, Conductivity, TOC, Coliform and Nitrates) and/or Product Testing (Bioburden, Endotoxin, Host Purity, or Non-Host), preferred

Skills / Abilities:

• Demonstrate the capability for continued upward growth and technical contributions
• Good analytical and problem-solving skills with proven ability to think critically and to focus on details of execution
• Good understanding of current FDA, EU and ICH requirements and implementation for GLP and GMP in the pharmaceutical industry
• Effective team and interpersonal skills with the ability to work across numerous scientific and management disciplines
• Experience in trending analytical data (method data and product data) is preferred
• Experience in trending environmental monitoring/clean room services data is preferred
• Experience in participating and supporting regulatory inspections through explanations of methodologies, investigations, and/or laboratory systems is preferred
• Good technical writing skills
• Experience authoring and reviewing technical documents such as reports and protocols
• Strong Computer Skills
• Microsoft Suite proficiency

Qualifications

• BA/BS in Life sciences field is required
• 4+ years of relevant experience in a CDMO and/or pharmaceutical environment
• Experience in laboratory testing, preferably in the pharmaceutical or biotechnology industries

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