Biomedical Engineer Part Time Jobs in Columbus, OH

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Job Title: Validation Specialist
Job Description
The Validation Specialist supports the qualification and validation of laboratory and manufacturing equipment, systems, and processes within a state-of-the-art life sciences facility. This role begins with hands-on work in temperature mapping, periodic review, pipette validation, and biosealer validation, and progresses to the validation of bioreactors over time. The Validation Specialist works across quality laboratories, cleanrooms, and warehouse areas to ensure equipment and processes meet regulatory, quality, and internal compliance standards. This position is well-suited for recent graduates or early-career professionals in life sciences or engineering who are eager to grow their expertise in equipment validation and Good Manufacturing Practice (GMP) environments.
Responsibilities

• Perform temperature mapping, periodic reviews, pipette validation, and biosealer validation, gradually expanding responsibilities to include bioreactor validation.
• Develop and execute equipment qualification protocols for manufacturing, processing, and filling equipment, as well as facilities and utilities that support these operations.
• Support project-based validation activities, completing one project before moving to the next, such as validating multiple pieces of laboratory equipment for new cleanroom openings.
• Analyze data generated by validation studies using statistical methods to determine process capabilities and assess performance.
• Gather and organize relevant documentation, including executed batch records, certificates of analysis, equipment logs, equipment qualifications, and raw material certificates of analysis.
• Investigate and resolve deviations or exceptions from predefined acceptance criteria identified during validation and qualification activities.
• Draw conclusions from data, observations, deviations, exceptions, and investigations to determine whether a process is considered valid.
• Review calibration and qualification records supplied by third-party vendors to ensure completeness, accuracy, and compliance.
• Author and review department standard operating procedures (SOPs) to support validation and qualification activities.
• Author, review, and execute User Requirements Specifications (URS), Functional Design Specifications (FDS), Risk Assessments (RA), Design Qualifications (DQ), and qualification test protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Write clear and comprehensive summary reports and closeout reports for validation and qualification protocols in accordance with established validation and qualification procedures and policies.
• Maintain protocols and system documentation in an orderly library so that information can be readily provided to regulatory bodies when required.
• Ensure that protocols, verifications, validation plans, and summary reports generated during validation and qualification activities are stored and archived according to internal procedures.
• Maintain current knowledge in compliance, validation, and relevant regulatory requirements by engaging with quality assurance, quality control, regulatory sources, professional periodicals, and appropriate training programs.
• Work proactively to uphold a high level of compliance in all validation-related activities and recommend improvements where appropriate.
• Develop and execute cleaning validation and verification protocols for manufacturing and processing equipment to ensure consistent and compliant operations.

Essential Skills

• Education in a relevant discipline such as Life Science, Chemical Engineering, Biomedical Engineering, or Biochemical Engineering.
• Open to entry-level graduates or individuals with 0-2 years of industry experience.
• Some prior work experience, which may include part-time roles or positions held during school, demonstrating reliability and professional behavior.
• Ability to work with laboratory equipment and follow detailed procedures for validation and qualification.
• Strong attention to detail and documentation skills for compiling batch records, certificates, logs, and validation reports.
• Capability to analyze data using basic statistical methods to evaluate process capabilities and validation outcomes.
• Effective written communication skills to author and review SOPs, URS, FDS, RA, DQ, and IQ/OQ/PQ protocols, as well as summary and closeout reports.
• Ability to investigate deviations and exceptions, identify root causes, and document findings and conclusions clearly.
• Organizational skills to maintain orderly validation libraries and ensure proper storage of protocols, plans, and reports.
• Motivation to learn and maintain up-to-date knowledge in compliance, validation practices, and relevant regulatory guidance.

Additional Skills & Qualifications

• Prior hands-on experience working with laboratory equipment.
• Any industry experience in life sciences, pharmaceuticals, or related fields.
• Familiarity with Good Manufacturing Practice (GMP) environments and regulatory expectations.
• Exposure to FDA-regulated or pharmaceutical settings.
• Knowledge of equipment validation concepts and practices, including IQ, OQ, and PQ.
• Understanding of or experience with cleaning validation and verification activities.
• Interest in working with bioreactors and complex manufacturing or processing equipment.
• Experience reviewing calibration or qualification records from third-party vendors.
• Comfort working in project-based environments, managing multiple validation tasks over time.

Work Environment
The Validation Specialist works in a modern, state-of-the-art facility that supports rapid growth in the life sciences sector. The role involves time spent in cleanrooms, quality laboratories, warehouse areas, and dedicated desk space. Approximately 25% of the workday is spent within various laboratory and controlled environments performing hands-on validation and qualification activities, while about 75% is spent at a desk performing data analysis, documentation, protocol development, and report writing. The position involves regular interaction with laboratory equipment, manufacturing and processing systems, and supporting utilities, with a strong emphasis on compliance, quality, and safety throughout all work areas.
Job Type & Location
This is a Contract to Hire position based out of Columbus, OH.
Pay and Benefits
The pay range for this position is $24.00 - $26.00/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 Columbus,OH.
Application Deadline
This position is anticipated to close on May 27, 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.
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