Description + Independently initiate, investigate, and complete Minor and low/medium severity Major deviations. + Collaboratively support high severity Major and Critical deviations under supervision. + Translate complex scientific events into clear, concise, and cohesive technical reports. + Conduct Root Cause Analysis (RCA), risk assessments, and impact evaluations on product quality (SISQP). + Identify and implement Corrective and Preventive Actions (CAPAs) to prevent recurrence. + Perform data gathering, trend analysis, cause mapping, and associate interviews. + Facilitate and participate in cross-functional meetings, alignment sessions, and deviation review boards. + Communicate investigation status and outcomes to internal teams and external clients through presentations and reports. + Work on the manufacturing floor to observe processes and collect data for investigations. + Manage multiple investigations and timelines, escalating issues as needed to ensure timely resolution. Skills + Laboratory, Biology, Gmp, Quality control, Microbiology Top Skills Details + Laboratory,Biology,Gmp Additional Skills & Qualifications + Bachelor’s degree in a scientific or technical discipline required. + 3+ years of experience in a GMP-regulated environment, preferably in manufacturing or quality. + Strong technical writing skills with the ability to communicate complex topics to a broad audience. + Proficient in root cause analysis tools, risk assessment methodologies, and deviation management systems. + Experience with client-facing communication, including presentations and facilitated reviews. + Ability to manage multiple priorities in a fast-paced, cross-functional environment. Preferred Skills: + Experience with TrackWise or similar quality management systems. + Strong facilitation and conflict resolution skills. + Familiarity with SISQP principles and regulatory compliance standards. + Positive, proactive, and adaptable mindset with a focus on continuous improvement. Experience Level + Intermediate Level Pay and Benefits The pay range for this position is $20.69 - $24.82/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 Houston,TX. Application Deadline This position is anticipated to close on Aug 11, 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.