Research Analyst II

Overview

The Global Material and Parenteral Packaging Sciences team-part of the Product Development Science & Technology (PDS&T) organization-is seeking a highly motivated Research Analyst II to support the development of Container Closure Systems (CCS) for novel parenteral and biotechnological products. This role directly contributes to the advancement of AbbVie's key pipeline programs, including monoclonal antibodies, antibody-drug conjugates, and therapeutic toxins.

The successful candidate will apply scientific and technical expertise to characterize CCS components (vials, prefilled syringes, cartridges) with a strong emphasis on Container Closure Integrity (CCI), process capability, and method development.

Key Responsibilities

• Prepare, execute, and evaluate laboratory experiments supporting the development of CCS for new parenteral drug products, including vials, prefilled syringes, cartridges, and lyophilized products.

• Perform technical evaluation, implementation, and continuous improvement of CCI and process methods in accordance with holistic CCI strategy and current regulatory expectations.

• Conduct performance analyses using force analyzers and support method development, qualification, and validation activities.

• Maintain laboratory equipment, ensuring compliance with maintenance schedules, documentation standards, and required training.

• Provide technical support for innovative CCS landscaping programs, including implementation and characterization using various CCI techniques.

• Collaborate with internal AbbVie partner laboratories, external laboratories, and pharmaceutical manufacturing sites to support CCS and process qualification.

• Coordinate suppliers for materials, instrumentation, and services necessary for laboratory operations.

• Document all work in compliance with applicable GxP guidelines and internal procedural requirements.

• Author comprehensive, scientifically robust laboratory reports, development reports, and risk assessments suitable for regulatory submissions.

• Adhere to all relevant safety standards and promote safe laboratory practices.

• Demonstrate ability to work independently, adapt to evolving project priorities, and proactively drive projects to completion.

Qualifications

• Bachelor's degree in pharmacy, biology, biotechnology, chemistry, process engineering, material sciences, physics, or related scientific discipline, with 2+ years of relevant experience; or a Master's degree with no additional experience required.

• Strong technical and scientific understanding of parenteral drug product development and Container Closure Integrity (CCI) test methods.

• Ability to interpret scientific literature and apply theoretical principles to solve problems within the relevant scientific discipline in a timely manner.

• Demonstrated ability to manage multiple projects concurrently, work effectively in team environments, and navigate shifting priorities.

• Strong verbal and written communication skills with the ability to prepare detailed scientific and project documentation.

• High level of motivation, strong attention to detail, and a proactive approach to laboratory responsibilities.

Preferred / Nice-to-Have Skills

• Experience working in regulated environments (GxP, GMP).

• Previous work in a laboratory, manufacturing, or R&D setting.

• Prior hands-on experience with CCI techniques (e.g., vacuum decay, helium leak, MicroCT).

• Familiarity with analytical instrumentation and testing techniques.

• Understanding of process qualification within pharmaceutical manufacturing.

Additional Skills Not Required

(Included only because they were referenced but not applicable to this role)

• Experience with UX, SEO, Tableau, or dashboard development.

• Familiarity with data visualization or reporting best practices.

Job Type & Location

This is a Contract position based out of North Chicago, IL.

Pay and Benefits

The pay range for this position is $30.00 - $34.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in North Chicago,IL.

Application Deadline

This position is anticipated to close on Feb 20, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.