{"id":2796729,"url":"https://alion.io/job/teva-quality-control-analyst-ii-2","title":"Quality Control Analyst II","company":{"id":1822915,"name":"Teva","domain":"teva.com","url":"https://alion.io/company/teva-com","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Eightfold","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"middle","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Cincinnati, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":57000,"max_usd":104000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":3690},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":true,"technologies":[],"status":"live","first_seen_at":"2026-07-28T19:30:12Z","employer_posted_date":"2026-10-14","last_verified_at":"2026-10-20T01:43:08Z","board_verified":true,"closed_at":null,"days_open":83,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":83},"description":"We Are Teva\nWe’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.\nOur Team, Your Impact\nFinished product team is looking to add an experienced analyst with a high understanding of instrumentation and a desire to be multifunctional within the team. They will be performing critical testing on the release of pharmaceuticals for human consumption along with ensuring that instrumentation is maintaned, qualified, calibrated and in good working order.\nHow You’ll Spend Your Day\nPerform routine and non-routine chemical testing of commercial, validation and stability samples in accordance to written methodology\nPerform qualitative and quantitative analyses using analytical instrumentation such as HPLC; GC, UV/Vis, KF and FTIR. \nUtilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data \nAnalyze data against approved specifications, notifying management of any OOS and aberrant results\nActively participate in root cause problem solving during laboratory investigations, provide input for effective corrective and preventive actions\nPerform routine maintenance on lab equipment as needed\nPerform metrology calibrations and preventative maintenance tasks, as needed\nKnowledge and understanding of USP, cGMP, and FDA regulations\nCreate and maintain lab record documentation (notebooks and computer based) according to GMPs\nDemonstrate the philosophy of Right First Time\nMaintain a clean and safe work environment and follow safety procedures and policies\nProvide feedback on systems and processes to promote continuous improvement and champion selected changes\nGrow in the job, accountable for establishing and accomplishing annual personal development goals\nCommunicate clearly and well within a team environment\nParticipate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives \nShares information with others - keeping management informed and helping department to meet the goals\nActively participate in regular one-on-one meetings with direct supervisor\nCommunicate external to the department and vendors\nCollaborate effectively to achieve team and organizational goals\nYour Skills and Experience\nAny equivalent combination of education, training, and/or experience that fulfills the requirements of the position will be considered.\nEducation/ Experience\nBachelors degree required\nA minimum of 3 years of experience in a pharmaceutical environment or similar regulated environment\nKnowledge/ Skills/ Abilities\nBasic knowledge and understanding of USP, cGMP and FDA regulations\nCreate and maintain lab record documentation (notebooks and computer based) according to GMPs\nMaintain a clean and safe work environment and follow safety procedures and policies.\nUse of Empower and intergrated LMS systems\nExperience calibrating HPLCS/GC Systems\nAbility to maintain, diagnose and work on laboratory instrumentation\nAlso Good to Have\nPrioritize assigned work to maximize time and equipment efficiency\nWork independently with limited supervision for routine assignments\nTroubleshoot problems encountered with methods and instruments - routinely solve, choosing among clearly defined alternatives\nResponsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation\nHow We’ll Take Care of You\nAt 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.\nWe offer a competitive benefits package, including:\nComprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls. \nRetirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan. \nTime Off: Paid Time Off including vacation, sick/safe time, caretaker time, 13 paid Holidays and 3 paid floating holidays. \nLife and Disability Protection: Company paid Life and Disability insurance. \nAdditional 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.\nAlready Working @Teva?\nMake sure to apply through our internal career site on Twist-your one-stop shop for career development\nTeva’s Equal Employment Opportunity Commitment\nTeva 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.\nPlease 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  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.\nImportant notice to Employment Agencies - Please Read Carefully\nTeva 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. 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