Job Title:

ScientistJob Description The Scientist will perform analytical testing on client samples using UV/Vis spectroscopy, filtration techniques, and microscopy in a regulated laboratory environment. This role focuses on generating high-quality data while ensuring all work complies with FDA regulations and cGMP standards. It is an excellent opportunity for professionals from pharmaceutical, medical device, biotech, contract testing, or other regulated laboratories who want to contribute to the expansion and build-out of a growing testing facility. Responsibilities

+ Perform analytical laboratory testing on client samples by following established standard operating procedures (SOPs) and approved test methods.

+ Analyze samples using UV/Vis spectroscopy to generate accurate and reliable quantitative and qualitative data.

+ Conduct filtration testing, including membrane filtration, particulate evaluations, and related filter integrity assessments.

+ Use microscopy to examine and identify particles, contaminants, and key sample characteristics.

+ Record and review laboratory data in compliance with cGMP and Good Documentation Practices (GDP), ensuring data integrity and traceability.

+ Maintain accurate laboratory records and enter results into laboratory information management systems (LIMS) or electronic lab notebooks (ELN) when applicable.

+ Ensure all testing activities align with FDA and other relevant regulatory requirements and internal quality standards.

+ Prepare reagents, solutions, and standards needed for routine and specialized testing activities.

+ Maintain, calibrate, and troubleshoot laboratory equipment to support consistent and reliable operation.

+ Participate in investigations involving out-of-specification (OOS), out-of-trend (OOT) results, deviations, and other quality events.

+ Assist with updating SOPs and supporting audits, inspections, and continuous improvement initiatives within the laboratory.

+ Contribute to the ongoing expansion of testing services by supporting new methods, technologies, and process improvements as the laboratory grows. Essential Skills

+ Bachelor's degree in chemistry, biology, materials science, or a closely related scientific discipline. + 1-3 years of hands-on laboratory experience in a GMP-regulated laboratory environment.

+ Industry experience performing UV/Vis spectroscopy for analytical testing.

+ Practical experience with filtration testing, including membrane filtration, particulate testing, and filter integrity testing.

+ Experience using microscopy to identify and characterize particles and contaminants in samples.

+ Familiarity with maintaining a lab notebook or working within an electronic lab notebook (ELN) system.

+ Working knowledge of cGMP requirements and Good Documentation Practices (GDP) in a regulated laboratory setting.

+ Ability to follow detailed SOPs and test methods accurately and consistently.

+ Strong attention to detail and commitment to data integrity and regulatory compliance. Additional Skills & Qualifications

+ Experience working in a contract testing laboratory environment.

+ Instrumentation experience with HPLC, FTIR, and particle sizing equipment.

+ Exposure to method validation or technology transfer activities within a regulated setting.

+ Prior experience authoring CAPA (Corrective and Preventive Action) investigations.

+ Familiarity with USP, EP, and ICH guidelines and understanding of FDA regulatory expectations.

+ Ability to support audits and contribute to continuous improvement initiatives in the laboratory.

+ Strong problem-solving skills and ability to participate effectively in OOS, OOT, and deviation investigations. Work Environment The role is based in a brand-new contract testing laboratory that focuses on supporting pharmaceutical and medical device clients. The team is in an early growth phase and is adding key roles to help build out the business and expand testing services. You will work with modern analytical instrumentation and laboratory systems in a cGMP-compliant environment, collaborating closely with other scientists and quality-focused professionals. The setting offers the opportunity to influence laboratory processes and contribute to a culture of continuous improvement and scientific excellence. Job Type & Location This is a Contract to Hire position based out of Minnetonka, MN. Pay and Benefits The pay range for this position is $25.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Minnetonka,MN.

Application Deadline This position is anticipated to close on Sep 18, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.