Junior Quality Control Analyst (GMP Lab)

Teva Pharmaceuticals; Cincinnati (OH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

401(k) retirement plan

Paid time off

Job summary

Teva Pharmaceuticals in Cincinnati is seeking a skilled analytical chemist to perform routine and non-routine testing of commercial, validation, and stability samples. You will use HPLC, GC, UV/Vis, KF, and FTIR instruments, with LIMS and Empower for data processing, ensuring compliance with cGMP standards.

Join a collaborative team focused on accuracy, documentation, and continuous improvement. A Bachelor’s in a science field and prior cGMP lab experience are required, with opportunities for

Qualifications

• Bachelor's in science related discipline (Chemistry is preferred)
• Experience in a cGMP laboratory

Responsibilities

• Perform routine and non-routine chemical testing of commercial, validation and stability samples in accordance to written methodology
• Perform qualitative and quantitative analyses using analytical instrumentation such as HPLC; GC, UV/Vis, KF and FTIR.
• Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data
• Analyze data against approved specifications, notifying management of any OOS and aberrant results
• Actively participate in root cause problem solving during laboratory investigations, provide input for effective corrective and preventive actions
• Perform routine maintenance on lab equipment, as needed
• Perform peer review of laboratory testing, as required
• Demonstrate knowledge of USP, cGMP, and FDA regulations
• Create and maintain lab record documentation according to GMPs and GLPs
• Demonstrate the philosophy of Right First Time
• Maintain a clean and safe work environment and follow safety procedures and policies
• Provide feedback on systems and processes to promote continuous improvement and champion selected changes
• Grow in the job, accountable for establishing and accomplishing annual personal development goals
• Contribute to department and site goals
• Communicate clearly within a team environment
• Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives
• Share information with others – keeping management informed and helping department to meet the goals
• Actively participate in regular one-on-one meetings with direct manager
• Communicate external to the department, where applicable
• Collaborate effectively to achieve team and organizational goals
• Prioritize assigned work to maximize time and equipment efficiency
• Work independently with limited supervision for routine assignments
• Troubleshoot problems encountered with methods and instruments
• Responsible for accurate, timely and compliant execution of assigned projects, analytical testing and related documentation

Skills

Analytical testing

HPLC

GC

LIMS

Empower

GMP compliance

Education

Bachelor's in science related discipline (Chemistry preferred)

Tools

HPLC

GC

UV/Vis

KF

FTIR

LIMS

Empower

Job description

Teva Pharmaceuticals in Cincinnati is seeking a skilled analytical chemist to perform routine and non-routine testing of commercial, validation, and stability samples. You will use HPLC, GC, UV/Vis, KF, and FTIR instruments, with LIMS and Empower for data processing, ensuring compliance with cGMP standards.

Join a collaborative team focused on accuracy, documentation, and continuous improvement. A Bachelor’s in a science field and prior cGMP lab experience are required, with opportunities for