{"id":2889969,"url":"https://alion.io/job/teva-qc-analyst-2","title":"QC Analyst","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":{"grade":"B","score":82,"open_postings":15,"ghost_share":0,"stale_share":0.733,"repost_share":0,"time_to_fill_p50_days":53,"computed_at":"2026-11-06T05:58:05Z"}},"role":"Biotech","role_family":"Biotech","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Troyan, Bulgaria"],"countries":["BG"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-06-02T10:30:22Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-06T13:43:20Z","board_verified":true,"closed_at":null,"days_open":157,"trust":{"level":"ok","repost_count":0,"flags":[],"days_open":156},"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\nThis QC Analyst is responsible for developing, validating, and supporting analytical methods and testing activities for pharmaceutical products, ensuring compliance with regulatory requirements and quality standards throughout product transfer and lifecycle management. The position also prepares analytical documentation for regulatory submissions, collaborates with cross-functional teams, and maintains laboratory operations, equipment, and compliance systems.\nHow You’ll Spend Your Day\nDevelop, validate, optimize, and transfer analytical methods for pharmaceutical products, including preparation of protocols, reports, and supporting documentation.\nPrepare analytical sections of regulatory submissions (CTD format) and support responses to regulatory authority inquiries.\nPerform stability studies, routine analytical testing, and release analyses for pharmaceutical products in compliance with applicable guidelines and regulations.\nPrepare and maintain analytical documentation, including SOPs, specifications, certificates of analysis, validation reports, and laboratory records.\nOperate, maintain, and support qualification of analytical equipment, including preparation of user requirement specifications (URS) for new laboratory instruments.\nCollaborate with cross-functional teams on product transfer projects, regulatory activities, and implementation of new laboratory systems and software.\nEnsure compliance with GMP, pharmaceutical standards, safety procedures, documentation requirements, and laboratory housekeeping practices.\nYour Skills and Experience\nBachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.\nMinimum 1 year of experience in pharmaceutical manufacturing, quality control, analytical development, or a similar laboratory environment.\nKnowledge of analytical method development, validation, stability testing, and pharmaceutical laboratory practices.\nFamiliarity with international regulatory requirements and pharmacopoeias, including Ph. Eur., USP, BP, ICH, EMA, and FDA guidelines.\nProficiency in Microsoft Office and experience working with electronic laboratory and documentation systems.\nGood command of English, both written and verbal.\nStrong problem-solving, collaboration, communication, and organizational skills, with a proactive and results-oriented approach.\nHow We’ll Take Care of You\nDynamic and challenging work environment in the leading pharmaceutical company in the world and the biggest pharmaceutical company in Bulgaria\nCompetitive remuneration with bound performance\nOpportunity for development\nJob specific training\nFood allowance\nOrganized transport Lovech-Troyan-Lovech\nAlready Working @Teva?\nIf you are a current Teva employee, please apply using the internal career site available on \"Employee Central\". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site\nThe internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.\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. 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