Job Description
This is a part-time position offering flexibility with work hours, ranging from 20 to 40 hours per week, with a preference for onsite presence at least two days a week, ideally between Tuesday and Thursday. The role involves performing data verification, data analysis, and managing documentation for health authority submissions.
ResponsibilitiesPerform data verification of analytical and process raw data, data analysis, reports, and health authority submissions.Manage, track, and monitor the data verification workload, including forecasting, progress tracking, and deliverables.Coordinate associated documentation by preparing, editing, proofreading, adjudicating reviewer comments with authors and subject matter experts, and uploading into the document management system.Evaluate and suggest improvements for current procedures and best practices for the Biologics program.Collaborate with teams across Quality Assurance, Process Development, MSAT, and Contract Manufacturing Organizations.Support special projects as assigned.Essential SkillsStrong attention to detail and quality mindset.Excellent verbal and written communication skills.Strong organizational skills.Understanding and application of GMP principles, concepts, and practices.Knowledge and familiarity with biologic manufacturing processes and terminology.Knowledge and familiarity with analytical methods, data, and terminology.Knowledge and familiarity with process validation in highly regulated manufacturing environments.Work Environment
The position offers flexibility with a part-time schedule, typically around 20 to 25 hours per week, up to 40 hours depending on workload and schedule needs. Ideally, two days onsite are required between Tuesday and Thursday. Consultants are given the option to take on additional projects if they desire, and schedules are generally determined a couple of weeks in advance.
Pay and BenefitsThe pay range for this position is $35.00 - $45.00/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 hybrid position in Foster City,CA.
Application Deadline
This position is anticipated to close on Jul 17, 2025.
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 actalentaccommodation@actalentservices.com for other accommodation options.