Quality Control Analyst I

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

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You’ll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You’ll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

How You’ll Spend Your Day

• 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
• Basic knowledge and understanding of USP, cGMP, and FDA regulations
• Create and maintain lab record documentation (notebooks and computer based) 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 and well within a team environment
• Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives
• Shares 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 - routinely solve, choosing among clearly defined alternatives
• Responsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation

Your Skills And Experience

Any equivalent combination of education, training, and/or experience that fulfills the requirements of the position will be considered.

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

How We’ll Take Care Of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

We Offer a Competitive Benefits Package, Including

• Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
• Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
• Time Off: Paid Time Off including vacation, sick/safe time, caretaker time, 13 paid Holidays and 3 paid floating holidays.
• Life and Disability Protection: Company paid Life and Disability insurance.
• Additional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to [e-mail] with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.

Important notice to Employment Agencies - Please Read Carefully

Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.