Manufacturing Associate

Job Title:

Manufacturing Associate Job Description We are seeking a passionate and curious Manufacturing Associate to join our dynamic team. This role is ideal for individuals who thrive on tackling new challenges, solving complex problems, and continuously learning. As a Manufacturing Associate, you will have the opportunity to drive impactful projects, collaborate with innovative minds, and explore new avenues. Your curiosity will not only fuel your personal growth but also contribute to the team's success. Responsibilities Execute process recipes and monitor equipment and processes. Perform basic tasks, including sampling and routine maintenance of lab equipment. Assist in media and buffer compounding. Comply with written procedures for safety requirements, cGMP practices, standard operating procedures, and manufacturing documentation. Perform and monitor critical processes such as single-use bioreactor operations, perfusion, chromatography, product filtration, and solution preparation. Support the introduction of new products and technologies into the facility. Initiate non-conformances (NC). Execute Electronic Batch Records (EBR) using the Manufacturing Execution System (MES). Draft and revise manufacturing procedures and standard operating procedures as necessary. Support operations of glasswasher and autoclave. Perform other duties as assigned. Essential Skills Strong focus on right the first time and attention to detail. Effective task/time management organizational skills. Capacity to develop solutions to technical issues of moderate scope. Ability to organize, analyze/interpret, and effectively communicate individual results. Motivated, self-starter with strong mechanical aptitude. Good interpersonal, team, and communication skills. Excellent oral and written communication skills. Additional Skills & Qualifications Bachelor's degree in Science or Engineering; or Associate's degree in a science-related area and relevant experience; or High school diploma or GED and 3+ years of relevant experience. 3+ years experience within the Biotech/Pharmaceutical industry supporting Downstream Manufacturing Operations. Experience with UF/DF Filtration and Tangential Flow Filtration techniques SAP Production Data Specialist. Experience in drug manufacturing documentation processing. Work Environment The role is 100% onsite in Redmond, WA, supporting drug manufacturing in a GMP environment. The facility operates 24 hours a day with day, swing, and night shifts. Day shift runs from Wednesday to Saturday (7:00am

• 6:00pm), swing shift from Wednesday to Saturday (12:00pm
• 11:00pm) with a 10% premium above base pay, and night shift from Wednesday to Friday with every other Saturday (7:00pm
• 8:00am) We reserve the right to pay above or below the posted wage based on factors unrelated to sex, race, or any other protected classification.

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. This temporary role may be eligible for the following: Medical, Dental & Vision 401(k)/Roth Basic/Supplemental Life & AD&D Short and long-term disability

HSA & DCFSA

Transportation benefits Employee Assistance Program Company Paid Time off or State Sick Leave Job Type & Location This is a Contract position based out of Redmond, WA. Pay and Benefits The pay range for this position is $30.00

• $42.00/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 Redmond,WA.

Application Deadline This position is anticipated to close on May 25, 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. 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.