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QUALITY ASSURANCE SPECIALIST

Salary

$52k - $58k

Min Experience

2 years

Location

Rosenberg, Texas, United States

JobType

full-time

About the job

Info This job is sourced from a job board

About the role

RESPONSIBILITIES: 

 

Documentation: 

 

  • Writes, and approves Non Conformances, deviations, OOS’s, &corrective action/preventative action (CAPA) management that impact plant operations and products and provide recommendations and corrective actions and effectiveness plans.
  • Performs problem analysis and CAPA management. 
  • Acts as a technical resource within the plant for problem solving, training on the Non Conformances/CAPA system, and continuous improvement.
  • Compiles required Non Conformances and CAPA metrics.
  • Assembles Non Conformanceand CAPA information for monthly and quarterly management review presentations.
  • Monitors and analyzes plant Investigation and CAPA metrics and information. Ensures all deadlines are met for action items. 
  • Completes customer complaint investigations as requested and per timelines provided.  
  • Ensures that Non Conformances/CAPA documentation is compliant with site and Corporate policy/procedure requirements. Ensures investigations are approved by correct areas.
  • Assists manufacturing and other departments in identifying root cause and implementing effective corrective actions for those circumstances where quality standards are not met. 
  • Trains new personnel on the Investigations and CAPA system. 
  • Coordinates with QA Manager to determine if batch will be a designated validation or stability batch.
  • Maintains the effectiveness of the investigation system.
  • Other related duties as assigned.

 

 

QUALIFICATIONS: 

 

  • Bachelor’s Degree, preferably in Science, Engineering, Math/statistics, or equivalent combination of education and experience. 
  • 2+ years of non-conformance investigation experience. 
  • 2+ years of experience in GLPor GMP environment.
  • 2+years experience reading, following, writing, reviewing, and approving SOP’s, protocols, technical reports for validations (methods, processes, & cleaning), protocols for equipment validations, summaries of data, annual summary reports for water systems, environmental monitoring, etc.
  • Proficient in MS Office suite of programs (Excel, Office, Outlook, Power-point,etc).
  • Able to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, decimals and percentages; calculate figures and amounts such as proportions and percentages; apply concepts of basic algebra and geometry.
  • Able to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
  • Strong organization, attention to detail, and communication skills, both written and verbal.
  • Able to work with others in a positive team environment.
  • Able to follow instructions and provide guidance and instruction to others.

 


At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. 

All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

About the company

Quality driven pharmaceutical company

Skills

Microsoft Office
Excel
PowerPoint
Word