Note: The job is a remote job and is open to candidates in USA. Teva Pharmaceuticals is a leading innovative biopharmaceutical company dedicated to addressing patients’ needs. They are seeking a Quality Control Analyst I to perform chemical testing and analyses, maintain laboratory records, and contribute to continuous improvement initiatives.
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
- 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
Skills
- 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
- BS or higher in science related discipline, chemistry is preferred
Benefits
- 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.
- 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
Company Overview
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