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Quality Assurance Specialist ll

TalentZok

San Diego, CA

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JOB DETAILS
SALARY
$29–$39 Per Hour
SKILLS
Analysis Skills, Biology, Biotech and Pharmaceutical, Chemistry, Communication Skills, Continuous Improvement, Corrective Action, Current Good Manufacturing Practice (cGMP), Detail Oriented, Documentation, FDA Requirements, GMP (Good Manufacturing Practices), Manufacturing, Manufacturing Operations, Microsoft Office, Multitasking, Operational Improvement, Operational Support, Organizational Skills, Procedure Development, Product Support, Production Control, Quality Assurance, Quality Control, Quality Management, Quality Metrics, Record Keeping, Regulations, Regulatory Compliance, Regulatory Requirements, Standard Operating Procedures (SOP), Team Player
LOCATION
San Diego, CA
POSTED
6 days ago
Quality Assurance Specialist II - Simply Biotech 

OVERVIEW 
Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the duties listed below. 
  
Immediate opening for a Quality Assurance Specialist II in San Diego, CA who possess: 
  • BS - Chemistry, Biology, Pharmaceutical Sciences
  • Quality Assurance Experience - 3+ yrs.
  • GMP level Audits/CDMO a +/pharma or biotech
 
Email resumes to

info@simplybiotech.com

 or call 949.204.3861. 
       
FULL DESCRIPTION: The Quality Assurance Specialist II supports quality and compliance activities within a regulated manufacturing environment. This role helps ensure products and processes meet established quality standards, regulatory requirements, and internal procedures. The successful candidate will have experience working in cGMP operations, strong attention to detail, and the ability to collaborate effectively across departments.
 
    
The selected candidate will be responsible for:    
  •  Review manufacturing and laboratory documentation to ensure accuracy, completeness, and compliance with quality standards.
  • Support material and product disposition activities in accordance with established procedures.
  • Assist with investigations related to deviations, quality events, corrective actions, and process changes.
  • Participate in audit preparation efforts and support regulatory inspection activities.
  • Ensure documentation practices comply with company procedures and regulatory expectations.
  • Work closely with Production, Quality Control, and other departments to address quality concerns and support operational improvements.
  • Maintain quality records and documentation within paper-based and electronic systems.
  • Assist with the creation, revision, and maintenance of standard operating procedures and related quality documents.
  • Provide quality oversight during manufacturing operations as needed.
  • Contribute to continuous improvement initiatives and other quality-related projects.
 
   
 The selected candidate will also possess:  
  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or another related scientific field; equivalent industry experience may be considered.
  • Approximately 3-5 years of experience in Quality Assurance within pharmaceutical, biotechnology, life sciences, or other regulated manufacturing environments. 
  • Experience working within cGMP quality systems is preferred. 
  • Understanding of applicable regulatory requirements, including FDA and international quality standards. 
  • Experience supporting investigations, CAPAs, document control, and quality system processes. 
  • Familiarity with electronic quality management systems (eQMS) and Microsoft Office applications. 
  • Strong organizational, analytical, and communication skills. 
  • Ability to manage multiple priorities and work effectively in a team-oriented environment. 
 
Salary Range: $29 to $39/hour

For immediate and confidential consideration, please email your resume to

info@simplybiotech.com

 or call 949.204.3861. 
  
More information can be found at www.simplybiotech.com. 
 


About the Company

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TalentZok

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