Job Title: Manufacturing Associate IIJob Description We are seeking a dedicated Manufacturing Associate II to perform critical manufacturing tasks involving reagents and buffers. The role requires troubleshooting formulations, filling processes, packaging, and analytical techniques. You will be responsible for conducting Quality Control procedures, performing data collection and analysis, processing work orders to complete products, and executing and improving batch records and SOPs. The position also involves identifying gaps and weaknesses in SOPs, maintaining inventory through cycle counts, and working collaboratively within a fast-paced environment. Responsibilities + Perform assigned manufacturing tasks for reagents and buffers. + Troubleshoot formulations, filling processes, and packaging. + Conduct Quality Control procedures for consumables. + Collect and analyze data. + Process work orders to complete products to inventory. + Execute and improve batch records and SOPs. + Identify gaps and weaknesses in SOPs and formulations. + Maintain correct inventory of materials through cycle counts, ordering, and receipt. + Operate in a fast-paced environment with rapidly shifting priorities. + Collaborate with scientists, engineers, and manufacturing personnel to support R&D and process improvement activities. + Fill support and kit support - able to lead a line. + Perform simple buffer formulation under 50L. + Other duties as assigned. Essential Skills + Proficiency in formulations, reagents, and Quality Control. + General laboratory skills including UV VIS. + Experience with SOPs, BRs, and WIs. + Hands-on experience with pH, conductivity meter, UV-vis, and standard lab equipment. + Strong analytical, verbal, and written communication skills using Excel, Word, and similar programs. Additional Skills & Qualifications + Experience with developing and updating BOMs is preferred. + Experience in formulation, fill, packaging, and chromatography in a laboratory setting is preferred. + Bachelor of Science degree in biology, biochemistry, chemistry, molecular biology, or other related life science discipline preferred. + 0-2 years of relevant experience in consumable manufacturing (an equivalent combination of experience and education may be considered). Work Environment This role operates within a multi-disciplinary startup focused on innovating genetic analysis tools for research and clinical markets. The work environment is characterized by improved data quality and simplified workflows that benefit discoveries and diagnoses in healthcare. The position is on the first shift, and you will be responsible for reagent formulation, quality control of reagent consumables, calibration, validation, and troubleshooting of equipment and instruments. Pay and Benefits The pay range for this position is $23.00 - $23.00/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 San Diego,CA. Application Deadline This position is anticipated to close on Jun 20, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.