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QA Analyst II
QA Analyst IIAlcon • Houston, TX, United States
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QA Analyst II

QA Analyst II

Alcon • Houston, TX, United States
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a QA Analyst II supporting our QC, Analysis and Test Service Team, you will be trusted to provide total quality management for the testing phase of the production process to ensure that final products meet the company standards at Houston, Texas in US.

Key Responsibilities :

  • Perform bioburden, endotoxin testing. and environmental monitoring.
  • Lead all aspects of routine monitoring program / special projects.
  • Perform biological indicator testing for annual requalifications.
  • Identify microorganism isolates recovered through characterization, gram stain, fungal stain, or through use of the Biolog Microorganism Identification system.
  • Support project related microbiological testing.
  • Qualify new laboratory equipment as needed.
  • Support laboratory team and daily microbiology laboratory operations, including lab organization / cleaning, routine equipment maintenance, supply inventory, media growth promotion etc.

Minimum Requirements :

  • Bachelor's Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)
  • The ability to fluently read, write, understand and communicate in English
  • Work hours : Monday through Friday / 8 : 00am - 5 : 00pm
  • Travel Requirements : 0 to 10%
  • Relocation assistance : No
  • Sponsorship available : No
  • Preferred Requirements :

  • Three (3) to Five (5) years applicable experience in the pharmaceutical field or related industry, a part of Quality Control Microbiology group preferred.
  • Proven excellent written / verbal / interpersonal / communication.
  • Ability to perform effectively in a fast paced, team-oriented environment.
  • Experience with laboratory requirements and equipment.
  • Bachelor's Degree in Science ( Microbiology or Biological Sciences).
  • Proficient in Microsoft Office (Word, PowerPoint, Excel, etc.).
  • Experience with Aseptic Technique, Bioburden Testing, Environmental Monitoring, Endotoxin Testing, and Gram and Fungal Stain.
  • Experience with Biolog Microorganism Identification System, Report Writing, Deviation Management.
  • Equipment Qualification and Standard Operating Procedure writing.
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