QC Associate I Microbiology
About The Position
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. Join Lonza in Vacaville, CA, as QC Associate I (Microbiology). This position will perform a broad variety of basic and moderate complex tests in support of GMP operations. Responsible for sampling of utility systems and manufacturing process spaces in Vacaville and performing a variety of chemical and microbiological analyses. Actively participate in continuous improvement to maintain company’s right to operate, supply to patients and cost effectiveness. Shift: Back Half Night: 8pm-6:30am What you will get: The full-time base annual salary for this position is expected to range between $65,000 to $105,000. 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 What you will do: Perform testing of routine and non-routine samples and documents according to GMP Review data and assess against established acceptance criteria, identify discrepancies. Provide input to design of quality investigations and CAPA initiatives as needed. Perform routine lab maintenance; order and maintain lab supply inventory. Receive and provide training Coordinate with customers to support operational activities, identify and support resolution of technical problems. Consistently meeting production schedules, actively participate in group and project teamwork; project and process improvements. Adhere to GMP policies and procedures, including documentation activities. What we are looking for: B.S./B.A degree in Life Science or related field. Experience is in pharmaceutical or biopharmaceutical industry desirable. Knowledge of assays/laboratory functions; prepare basic and complex. reagents as assigned. Experience working in a GMP environment. 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.
Requirements
- B.S./B.A degree in Life Science or related field.
- Knowledge of assays/laboratory functions; prepare basic and complex. reagents as assigned.
- Experience working in a GMP environment.
Nice To Haves
- Experience is in pharmaceutical or biopharmaceutical industry desirable.
Responsibilities
- Perform testing of routine and non-routine samples and documents according to GMP
- Review data and assess against established acceptance criteria, identify discrepancies.
- Provide input to design of quality investigations and CAPA initiatives as needed.
- Perform routine lab maintenance; order and maintain lab supply inventory.
- Receive and provide training
- Coordinate with customers to support operational activities, identify and support resolution of technical problems.
- Consistently meeting production schedules, actively participate in group and project teamwork; project and process improvements.
- Adhere to GMP policies and procedures, including documentation activities.
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
