Analytical Services Contractor

About the role

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.

Responsibilities

• Review laboratory notebooks from Analytical Development scientists for:
  • Completion and compliance with GDP
  • Accuracy and clarity of data
  • Suitability of analytical methods and data to support development goals
• Provide technical support for separation-based assays, including:
  • HPLC such as RPLC, AEX, CEX, HIC, etc.
  • GC
  • CE‑SDS
• Review and provide feedback on analytical methods, ensuring compliance with internal standards and GMP requirements.
• Assess and review qualification protocols and reports for analytical methods that are going to be transferred to quality control team for GMP manufacturing support and release testing.
• Support preparation and review of development reports.
• Review and assist in generation of Certificates of Testing (CoT) for development batch release and stability time points.
• Ensure data and documentation meet all regulatory and internal compliance standards.

Qualifications

• Bachelor’s degree or higher in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
• 5+ years of industry experience in analytical development or quality control within a regulated (GMP) biopharmaceutical or pharmaceutical environment.
• Strong working knowledge of separation-based analytical techniques, particularly HPLC, GC, and CE‑SDS.
• Demonstrated experience in reviewing laboratory notebooks, technical reports, and GMP documents.
• Familiarity with method development and qualification principles.
• Excellent attention to detail, strong organizational skills, and the ability to manage multiple priorities.
• Effective communication and collaboration skills for cross‑functional teamwork.
• Proficiency in document management systems is a plus.

Skills

• Experience with stability testing and strong familiarity with ICH guidelines, including but not limited to: ICH Q1A–