Quality Control Analyst, Environmental Monitoring

Quality Control Analyst, Environmental Monitoring

Location: This is an on-site position located in Pearland, TX.

The purpose of this role is to support the Quality Control, Environmental Monitoring team in maintaining the cleanrooms for aseptic manufacturing for both At Rest and In Operation conditions. This role will also be central in all processes associated with environmental monitoring and is integral with environmental investigations, excursion report writing, and general upkeep of the micro department.

Shift available: Sunday - Wednesday, 8am-6:30pm 

What you will get:

A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus.

• Medical, dental and vision insurance.

• 401(k) matching plan.

• Life insurance, as well as short-term and long-term disability insurance.

• Employee assistance programs.

• Paid time off (PTO).

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do:

• Performance of environmental monitoring. Level 3 gowning qualification is required. There will be events where many hours within the cleanroom at level 3 gowning is required. Work hours may vary dependent on the demands of individual manufacturing events.

• Assist with the maintenance of laboratory/media supplies and equipment.

• Support investigations for environmental excursions; assist and revise standard operational procedures, trend reports, deviations, and corrective actions.

• Perform water sampling and gas testing.

• Execute aseptic process validations, EM performance qualifications, and gowning qualifications.

• Inspect aseptic process qualification units.

• Maintains compliance with all required training and assists with training of fellow analysts.

What we are looking for:

• Bachelor's degree with concentration in Life Sciences or Microbiology/Biology.

• Intermediate knowledge in cGMP principles.

• Experience working in pharmaceutical industry, including aseptic gowning.

• Acquires and documents training on all laboratory general tasks and is capable of performing assigned test methods and using associated instrumentation.

• Understanding of basic laboratory equipment and aseptic technique a plus.

• Records test results and maintain raw data and accurate laboratory records.

• Experience in QC and environmental monitoring a plus.

About Lonza:

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.