Process Scientist

Job Title:

Process Scientist Job Description The Process Scientist I supports the Critical Raw Materials team by manufacturing liquid components used in in‑vitro diagnostic (IVD) products. This role focuses on immune‑system-based reagents such as antibodies, antigens, and serum proteins, which are produced, tested, and prepared for use on diagnostic analyzers. The position combines hands‑on laboratory work with documentation and coordination in a regulated, Good Manufacturing Practice (GMP) environment to help deliver accurate diagnostic solutions that improve patient outcomes. Responsibilities Perform material processing and reagent formulation for bulk intermediates and liquid components used in IVD products. Support the production of serum proteins and OEM liquid products according to established procedures and quality standards. Determine reprocessing needs for calibrators, controls, and antibodies with guidance from established protocols and senior team members. Maintain Good Laboratory Practices (GLP) and contribute to laboratory and equipment upkeep, including routine cleaning, organization, and basic maintenance. Conduct in‑process testing and final quality control (QC) for serum protein products, following documented methods and specifications. Assign calibrator values and control ranges to optimize diagnostic kit performance and ensure reliable analytical results. Monitor internal control supplies, proactively identify low inventory levels, and manufacture new controls as needed to support continuous production. Perform second‑checks on calculations, documentation, and test results to ensure accuracy, compliance, and data integrity. Use laboratory instruments such as pH meters, balances, and mixers to prepare and verify reagents and solutions. Document all laboratory activities accurately and thoroughly in compliance with regulated environment requirements and good documentation practices. Collaborate closely with a cross‑functional, highly collaborative team to support critical raw material supply for diagnostic products. Follow GMP and safety procedures consistently to maintain a controlled, compliant manufacturing environment. Essential Skills Bachelor's degree in Biology, Chemistry, Biochemistry, or a closely related scientific discipline. Ability to work effectively in a regulated environment and follow established procedures and standards. Experience with good documentation practices, gained through academic laboratory work or industry experience. At least 6 months of laboratory experience in an academic or industry setting. Hands‑on experience using laboratory equipment such as pH meters, balances, and mixers. Foundational knowledge of biochemistry, biology, or related laboratory sciences relevant to reagent preparation and testing. Experience with reagent preparation, pipetting, and basic laboratory techniques. High attention to detail and strong organizational skills to ensure accurate processing, testing, and documentation. Self‑starter with the ability to work independently while also contributing to a collaborative team environment. Motivation to perform work that directly improves patient lives through more accurate diagnosis. Comfort working within Good Laboratory Practices (GLP) and adhering to quality and safety standards. Additional Skills & Qualifications Experience working in a GMP manufacturing environment. Previous manufacturing experience in either GMP or non‑GMP settings. Exposure to or experience with in‑vitro diagnostics (IVD) products and processes. Previous experience in biotech, reagent production, or related life science manufacturing. Familiarity with quality control processes for reagents and diagnostic components. Understanding of immune‑system-based reagents such as antibodies, antigens, and serum proteins. Strong communication skills to interact effectively with cross‑functional teams and support collaborative problem‑solving. Demonstrated reliability and strong work ethic, as verified by references. Work Environment This role operates within a GMP manufacturing environment that supports the production of critical raw materials for diagnostic products. The position is primarily first‑shift, Monday through Friday. The team typically starts as early as 5:00 a.m., with flexibility to accommodate a later start time around 7:00 a.m. if needed. Approximately 80% of the work is hands‑on in the laboratory, involving material processing, reagent formulation, in‑process testing, and final QC activities. The remaining 20% is desk‑based, focused on documentation, data review, and coordination. You will work with laboratory technologies and equipment such as pH meters, balances, mixers, and other standard lab instruments in a fast‑paced, highly collaborative team environment. The role is initially open to cover family leave needs, with strong potential to transition into full‑time employment based on performance and organizational growth. The culture emphasizes collaboration, quality, and a shared commitment to improving patient outcomes through accurate diagnostics. Job Type & Location This is a Contract position based out of Stillwater, MN. Pay and Benefits The pay range for this position is $22.00 - $29.00/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 Stillwater,MN.

Application Deadline This position is anticipated to close on Jul 6, 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.