USA - Bioanalyst - II - USD

Pfizer; New Haven, Northern (CT, KY); Hybrid; USD 29,000 - 36,000; Full time

Job summary

Pfizer in New Haven, CT is seeking a Bioanalyst to conduct laboratory tests supporting research, development, and quality control in early-phase trials. The role blends office-based quality oversight (75%) with hands-on lab support (25%) during peak times, offering a development path into bioanalytical quality and operations.

The successful candidate will manage inventory, ensure data integrity, and support GxP processes while collaborating with lab scientists and project leads in a fast-paced

Qualifications

• Bachelor's degree in biology, biochemistry, or a related field.
• 2–4 years of work experience in a laboratory setting preferred.

Responsibilities

• Enhance Operational Excellence through efficient use of lab inventory and asset management.
• Master GxP Document Lifecycle through use of lab procedural documents as well as submission-ready lab study plans and reports.
• Ensure Data Integrity through quality review of cumulative data tables against source.
• Drive Project Timelines through frequent communication and coordination with lab scientists and project leads and biweekly study management meetings.
• Provide Critical GxP Lab Support through routine qualification of equipment, software, and the processing/management of human biospecimens.

Skills

Analytical skills

Time management

Lab safety knowledge

Communication teamwork

Data analysis tools

Education

BSc in biology/biochemistry

Tools

Data analysis software

Job description

The main function of a Bioanalyst is to conduct laboratory tests and/or analyses to support research, development, and quality control in the life sciences. This will be a development opportunity to a lab generalist looking to specialize in bioanalytical quality and operations in an early-phase clinical trial unit. The position is primarily office-based (75%) with a focus on quality oversight while also requiring hands-on lab support (25%) during peak times.

Job Responsibilities

• Enhance Operational Excellence through efficient use of lab inventory and asset management.
• Master GxP Document Lifecycle through use of lab procedural documents as well as submission-ready lab study plans and reports.
• Ensure Data Integrity through quality review of cumulative data tables against source.
• Drive Project Timelines through frequent communication and coordination with lab scientists and project leads and biweekly study management meetings.
• Provide Critical GxP Lab Support through routine qualification of equipment, software, and the processing/management of human biospecimens.

Skills

• Strong analytical and problem-solving skills, Attention to detail and accuracy in data recording.
• Exceptional time management with ability to multi-task.
• Knowledge of laboratory safety and regulatory requirements.
• Effective communication and teamwork abilities.
• Familiarity with data analysis software and tools.

Education/Experience

Bachelor's degree in biology, biochemistry, or a related field required and 2-4 years of work experience in a laboratory setting preferred.

Pay Rate Range

• Min Pay Rate $21
• Max Pay Rate $26

Currency USD

Unit hourly

Additional Notes

Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.

This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.

Benefits Information

• Comprehensive Benefits Package available based on eligibility
• Short-Term Disability (STD)
• Long-Term Disability (LTD)
• Supplemental and Voluntary Life Insurance