Quality Control Microbiologist (Contract)

• 13659 HumanHire Sacramento, CA Job Details Contract $35
• $50 an hour 16 hours ago Benefits Flexible schedule Qualifications Biology Engineering equipment malfunctions diagnostics Teamwork Investigations regulatory compliance Defect resolution root cause analysis Cleanroom environmental monitoring Preventive action implementation Laboratory instrument validation Microbiology testing Production deviation management Laboratory experience Quality control preventive actions Corrective and preventive actions (CAPA) GMP Cleanroom protocols Internal investigations Personal protective equipment (PPE) adherence Industrial equipment troubleshooting Data summary reports Quality reports Manufacturing facility experience Production validation processes Bachelor's degree Scientific writing Cleanroom gowning procedures Quality assurance experience within pharmaceutical industry Regulatory/legal compliance standards in production Cleanroom experience Environmental monitoring Biomedical regulatory compliance Full Job Description Quality Control Microbiologist•(Contract) Remote/Flexible Schedule | Sacramento, CA (Hybrid as Needed) $35.

00

• $50.00 per Hour | 6-Month Contract (July
• December) We are seeking a Quality Control Microbiologist with 2-3+ years of GMP Quality Control experience in the biotechnology, pharmaceutical, cell therapy, or life sciences industry.

Required Experience:

2-3+ years of Quality Control Microbiology experience in a GMP-regulated environment Experience managing CAPAs (Corrective and Preventive Actions) , including investigating quality issues, identifying root causes, implementing corrective actions, and preventing recurrence Experience reviewing Environmental Monitoring (EM) deviations Experience reviewing Personnel Monitoring (PM) deviations Experience troubleshooting laboratory or manufacturing equipment Experience writing validation reports and supporting validation activities Working knowledge of FDA regulations, cGMP requirements, and Quality Management Systems (QMS) Quality Control Microbiologist (Contract) Join an innovative biotechnology company developing next-generation cell therapies that are transforming the lives of patients. We are seeking an experienced Quality Control Microbiologist to support our Quality team during a six-month contract assignment. This Quality Control Microbiologist position offers a flexible work schedule with the majority of work performed remotely. Occasional onsite work at one of our Sacramento facilities will be required based on operational needs. If you're passionate about GMP quality systems, microbiology, and supporting groundbreaking therapies, we'd love to hear from you. Why You'll Love This Opportunity $35.00

• $50.

00 per hour Approximately 6-month contract (July through December) Primarily remote with flexible work hours Opportunity to support cutting-edge cell therapy manufacturing Collaborative, mission-driven team environment Meaningful work that directly impacts patient lives Position Summary The Quality Control Microbiologist plays a critical role in maintaining and improving Quality Management Systems while ensuring products meet regulatory and quality standards prior to release. This individual will manage deviations, CAPAs, document control, validation activities, equipment troubleshooting, and batch disposition while partnering closely with Manufacturing, Quality Assurance, and Research teams. Key Responsibilities Quality Systems Management Manage quality systems including: Deviations Change Controls CAPAs (Corrective and Preventive Actions) Document Control Investigate quality events and determine root cause Implement and document corrective and preventive actions Review and approve change controls Track completion of quality records and quality metrics Environmental & Personnel Monitoring Review Environmental Monitoring (EM) results and deviations Review Personnel Monitoring (PM) results and investigate deviations Support investigations and implement corrective actions when required Equipment & Validation Troubleshoot laboratory and manufacturing equipment issues Support equipment qualification and validation activities Prepare and review validation reports Batch Disposition Review manufacturing batch records Evaluate documentation for product release Make timely batch disposition decisions Partner with Manufacturing and Quality teams to ensure products meet regulatory and quality standards Document Control Maintain controlled quality documentation Ensure documentation complies with FDA and cGMP requirements Perform periodic document reviews Regulatory Compliance Maintain compliance with FDA regulations and cGMP requirements Support internal and external audits Ensure quality systems remain audit-ready Training & Collaboration Train and mentor employees on quality systems and compliance Serve as a quality resource for cross-functional teams Promote continuous quality improvement initiatives Qualifications Required Bachelor's degree in Biology, Biochemistry, Immunology, Microbiology, or another related scientific discipline 2-3+ years of Quality Control, Microbiology, GMP Manufacturing, Analytical Development, or Pharmaceutical/Biotechnology Quality experience Strong understanding of FDA regulations, cGMP requirements, and Quality Management Systems Experience with CAPA investigations, deviation management, validation documentation, and equipment troubleshooting Preferred Cell therapy or biopharmaceutical manufacturing experience Internal audits Batch record review and disposition Document Control systems Environmental Monitoring (EM) Personnel Monitoring (PM) Quality Management Systems (QMS) We're Looking For Someone Who Has Excellent attention to detail and commitment to data integrity Strong organizational and documentation skills Ability to manage multiple priorities in a fast-paced GMP environment Strong written and verbal communication skills Excellent problem-solving and analytical abilities Ability to work independently and collaboratively with cross-functional teams Work Environment Majority of work performed remotely Flexible work schedule Must be available to work onsite at either Sacramento location as business needs require Comfortable participating in virtual meetings Occasional overtime, weekends, holidays, or on-call support may be required Physical Requirements Must meet cleanroom gowning requirements, including wearing appropriate PPE when onsite Visual acuity of 20/20 (corrected or uncorrected) Normal color vision required for inspection activities Must comply with all GMP cleanroom standards regarding PPE, cosmetics, jewelry, and gowning requirements Compensation $35.00

• $50.

00 per hour , based on experience and qualifications. Apply Today! If you're an experienced Quality Control Microbiologist with hands-on GMP experience, CAPA management, Environmental Monitoring, validation reporting, and equipment troubleshooting, we'd love to hear from you. Join a team developing innovative cell therapies that are changing patients' lives.

Pay:

$35.00

• $50.

00 per hour

Work Location:

Hybrid remote in Sacramento, CA 95837