1

Avant Assessment Jobs (NOW HIRING)

Azure Cloud Architect

Washington, DC · On-site

$180 - $240/hr

The chosen candidate will be instrumental in devising and executing avant-garde solutions, spanning ... Migration & Hybrid * Experience leading workload assessments with Azure Migrate and mapping ...

Mgr - Safety,Health,Environ

Manchester, PA · On-site

$77K - $104K/yr

At L'Oréal Professional Products Division, we have more than 115 years of avant-garde to define ... Trains and leads employees in risk assessment (SHAP), incident investigation, and effective post ...

Showing results 41-53

Avant Assessment information

See salary details

$31.5K

$117.2K

$147K

How much do avant assessment jobs pay per year?

As of Aug 21, 2026, the average yearly pay for avant assessment in the United States is $117,194.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,500.00 and $124,000.00 per year, depending on experience, location, and employer.

What is an Avant Assessment?

An Avant Assessment job typically involves evaluating language proficiency tests for various languages. Avant Assessment is a company specializing in language assessment, and jobs may include roles such as test raters, item writers, or administrative positions. Raters assess speaking and writing responses based on standardized scoring guidelines. Many positions are remote and require expertise in the language being evaluated.

What does a typical day look like for someone working at Avant Assessment?

A typical day for a professional at Avant Assessment often involves developing, reviewing, or scoring language proficiency assessments, collaborating closely with educators and curriculum specialists, and analyzing test data to ensure accuracy and fairness. You may also spend time maintaining assessment quality by participating in team meetings or professional development sessions. Teamwork and communication are central, as you'll often coordinate with test developers, technology staff, and client support teams. The environment is generally collaborative, with opportunities to contribute ideas for product improvement and innovation. If you enjoy a mix of independent analytical work and cross-functional teamwork, this role offers a dynamic and fulfilling routine.

What are the key skills and qualifications needed to thrive in the Avant Assessment position, and why are they important?

To thrive in a position with Avant Assessment, you generally need a background in language education, standardized assessment design, and linguistic proficiency, often supported by relevant degrees or teaching certifications. Familiarity with computer-based testing platforms, data analysis tools, and learning management systems is highly beneficial. Strong communication, attention to detail, and adaptability are key soft skills that set top performers apart. These qualifications ensure the development, administration, and evaluation of reliable language assessments that meet educational standards.

More about Avant Assessment jobs

What states have the most Avant Assessment jobs?

States with the most job openings for Avant Assessment jobs include:

Infographic showing various Avant Assessment job openings in the United States as of August 2026, with employment types broken down into 82% Full Time, 6% Part Time, and 12% Contract. Highlights an 100% In-person job distribution, with an average salary of $117,194 per year, or $56.3 per hour.

Senior Scientist II, Downstream Development (Scale-Up Laboratory Lead)

Allergan

South San Francisco, CA • On-site

$100 - $130/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


Job description

Job Description

The Biologics CMC Development team at AbbVie has a long and rich history of biologics development. Located in a new state‑of‑the‑art facility in South San Francisco, the team leverages its comprehensive end‑to‑end CMC capabilities to work collaboratively through all phases of CMC development with a primary focus on advancing biologic therapies, such as monoclonal antibodies, bi‑specifics and novel modalities, to human clinical studies and eventual licensure. This role is within a team of highly experienced scientists and managers who have directly enabled the development/IND submissions of 20+ novel oncology drugs and successfully filed two BLAs.

We are seeking a highly motivated Senior Scientist II to join the Downstream Development team as a Scale‑Up Laboratory Purification Leader. In this role, you will lead laboratory‑based scale‑up activities to develop, optimize, and transfer robust, phase‑appropriate downstream processes for biologic drug substance manufacturing. You will provide technical leadership across scale‑up and technology transfer activities while helping advance next‑generation purification platform capabilities.

This role requires strong technical expertise in downstream development, scale‑up and tech transfer, demonstrated leadership skills, and the ability to work effectively in a highly collaborative, team‑based, matrixed environment. This position is an onsite laboratory‑based role and is best suited for someone who thrives in close partnership with scientists, engineers, and manufacturing teams.

Responsibilities
  • Lead downstream scale‑up lab activities and non‑GMP material generation to support CMC development, optimization, and transfer of purification processes for biologic candidates across development stages.
  • Maintain operational readiness of the scale‑up lab, including equipment availability, workflow planning, consumables, and efficient activity scheduling.
  • Serve as a subject matter expert and technical lead for downstream scale‑up and technology transfer; collaborate with and provide technical guidance to project purification development representatives to support transfer to the scale‑up lab and GMP manufacturing.
  • Lead downstream technology transfer activities to internal manufacturing sites and external partners, including transfer package preparation, batch support, and resolution of scale‑up or execution issues.
  • Serve as an AKTA subject matter expert (AKTA Ready, AKTA Ready LX, AKTA Avant, AKTA Pure), including method development and execution using UNICORN software.
  • Drive scientific understanding and execution of downstream unit operations, including resin‑ and membrane‑based chromatography, filtration, viral clearance operations, high‑concentration UF/DF, and formulation.
  • Provide hands‑on leadership in large column packing (AxiChrom, QuickScale, BPG), buffer preparation, equipment setup, and unit operation execution.
  • Develop and implement scale‑up lab operational workflows, procedures and documentation to enable efficient, reliable, and compliant execution of downstream development activities.
  • Design and execute scale‑down and scale‑up studies to build process understanding, assess robustness, and improve manufacturing readiness.
  • Troubleshoot process and equipment issues efficiently; work closely with vendors to resolve problems and provide feedback to improve systems and workflows.
  • Identify and implement next‑generation purification platform strategies and workflow improvements to enhance scalability, robustness, efficiency, and cost effectiveness.
  • Partner effectively across a matrixed organization with upstream, analytical, drug product, manufacturing, and engineering teams.
  • Mentor junior scientists and, where applicable, manage direct reports through strong planning, communication, and scientific judgment.
  • Author and review technical reports, development summaries, transfer documentation, and regulatory support documents.
  • Work efficiently and collaboratively to meet program milestones while maintaining high standards for safety, documentation, and data integrity.
  • Promote a strong safety culture by ensuring scale‑up lab activities, equipment use, and material handling practices are executed in accordance with site safety and compliance requirements.
Qualifications Basic:
  • Degree in Chemical Engineering, Biochemistry, Chemistry, or other relevant scientific discipline with a B.S. and typically 12+ years of experience, M.S. and typically 10+ years of experience, or Ph.D. and typically 4+ years of experience.
  • Significant experience in downstream/purification process development within a biologics CMC environment.
  • Demonstrated expertise in process scale‑up, scale‑down model execution, and technology transfer.
  • Must be an AKTA systems expert, including deep hands‑on experience with UNICORN software.
  • Hands‑on experience operating large‑scale TFF processes (hundreds of grams; e.g., Allegro, Cytiva, Repligen, or manually operated skids), packing 3–20 L columns with affinity and polishing resins, using single‑use technologies (e.g., SUMs, pre‑packed columns, AKTA flow kits, TFF flow kits), operating large‑scale filtration processes including depth filtration, virus filtration, and chromatography membrane filtration, and executing large‑volume formulations.
  • Experience with large column packing, buffer preparation, equipment troubleshooting, and day‑to‑day laboratory execution.
  • Proven ability to troubleshoot equipment issues and work effectively with vendors on repairs, reliability improvements, and technical feedback.
  • Demonstrated leadership skills with ability to lead projects, influence decisions, and mentor others.
  • Working knowledge of analytical methods such as HPLC, CE, UV‑based quantitation, and impurity characterization used to support downstream development.
  • Must work effectively in a team‑based, highly collaborative, matrixed environment.
  • Strong written and verbal communication skills, including technical writing and scientific data presentation.
  • Ability to independently design, execute, and interpret experiments to solve complex technical problems.
  • Strong understanding of biochemistry and bioprocess engineering principles relevant to downstream development and scale‑up.
  • Strong attention to detail and documentation practices.
Preferred:
  • Experience leading or overseeing a downstream scale‑up laboratory or comparable technical development function.
  • Hands‑on experience supporting transfer of purification processes to pilot‑scale, GMP manufacturing, or external CDMOs.
  • Experience with monoclonal antibodies, bispecifics, or other complex biologic modalities across multiple scales.
  • Experience advancing platform purification strategies or implementing next‑generation technologies to improve robustness, cost, and efficiency.
  • Knowledge of statistical tools and data analysis approaches that support process understanding and scale‑up decisions.
Additional Information
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long‑term incentive programs.
Equal Opportunity Employer

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.

Contact

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation: https://www.abbvie.com/join-us/reasonable-accommodations.html

#J-18808-Ljbffr