{"id":3927030,"url":"https://alion.io/job/teva-assoc-dir-regulatory-affairs","title":"Assoc Dir Regulatory Affairs","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":"A","score":89,"open_postings":41,"ghost_share":0,"stale_share":0.439,"repost_share":0.024,"time_to_fill_p50_days":52,"computed_at":"2026-11-10T06:52:35Z"}},"role":"Biotech","role_family":"Biotech","seniority":"staff","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bengaluru, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":12,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-11-05T10:30:45Z","employer_posted_date":"2026-11-06","last_verified_at":"2026-11-10T18:03:48Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"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\nThe Associate Director, Regulatory Affairs - APAC Lifecycle Management is responsible for leading a team of Regulatory Affairs professionals supporting post-approval and lifecycle management activities across the Asia-Pacific (APAC) region. The role provides strategic and operational leadership for regulatory maintenance activities, ensuring compliance, regulatory excellence, and uninterrupted product supply across a diverse portfolio of innovative medicines, biologics, biosimilars, and/or generic products. The role is expected to partner closely with market RA regulatory affairs, global regulatory, CMC, labeling, safety, supply chain, quality, and commercial stakeholders.\nHow You’ll Spend Your Day\nLeadership & People Management\nLead, coach, and develop a team of Regulatory Affairs professionals supporting APAC lifecycle management activities\nEstablish a centralized hub model with clear objectives, performance expectations, and development plans for team members.\nFoster a culture of accountability, collaboration, innovation, and continuous improvement.\nBuild regulatory capabilities and succession plans across the organization.\nDrive employee engagement and talent development within the team.\nRegulatory Strategy & Execution\nDevelop and oversee regulatory lifecycle strategies across APAC markets, support individual markets as per business need with regulatory submissions.\nEnsure timely execution of post-approval submissions, including:\nVariations and amendments\nManufacturing and site changes\nLabeling updates\nSafety-related updates\nRenewals and license maintenance activities\nProduct transfers and divestments\nAssess regulatory risks and develop mitigation strategies.\nPortfolio & Compliance Management\nEnsure continuous regulatory compliance and maintenance of product registrations across APAC markets.\nMonitor upcoming regulatory commitments, regulatory intelligence, and submission requirements.\nMaintain inspection readiness and support responses to regulatory agency requests.\nEnsure robust tracking and management of regulatory commitments, approvals, and implementation requirements.\nCross-Functional Collaboration\nPartner with Market Regulatory Affairs to ensure alignment of regional and global regulatory strategies.\nCollaborate with CMC, Quality, Supply Chain, Manufacturing, Pharmacovigilance, and Labeling teams to enable successful product lifecycle changes.\nSupport business continuity and product supply through proactive regulatory planning.\nServe as the primary regulatory representative for APAC lifecycle management initiatives for APAC markets.\nOperational Excellence\nDrive standardization, harmonization, and process improvements across APAC regulatory operations to establish the hub model across the team\nLeverage digital tools and regulatory information management systems to improve efficiency.\nMonitor team performance using KPIs and business metrics.\nLead resource planning and workload prioritization across the APAC portfolio\nYour Skills and Experience\nBachelor's degree in Life Sciences, Pharmacy, Biotechnology, Regulatory Affairs, or related discipline.\nAdvanced degree (MSc, PharmD, MBA, Ph.D or equivalent) preferred\n12-15 Years of Regulatory Affairs experience within the pharmaceutical; biotechnology, or related healthcare industry with 7+ years experience in direct people management.\nSignificant experience managing post-approval lifecycle activities across multiple APAC markets.\nPrior people leadership experience, including management of direct reports and geographically dispersed teams.\nExperience supporting innovative medicines, biologics, biosimilars, or generics portfolios.\nDemonstrated success leading complex cross-functional programs.\nGood leadership, project management and communication skills\nExcellent analytical, problem-solving, and self-learning skills.\nAbility to work independently and effectively in a cross-functional team environment; manage multiple projects simultaneously.\nDetail-oriented with a high level of accuracy in work deliverables.\nStrong organizational and time management skills.\nExcellent spoken and written English is essential\nHow We’ll Take Care of You\nAt Teva India, care is at the heart of how we work. From your first day, you’ll be welcomed into a people-first culture built on inclusion, respect, and belonging.\nThat support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You’ll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.\nYour growth matters too. You’ll have opportunities to build future-ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI-enabled Teva Twist program, R&D Academy, continuing education, and mentorship.\nJoin our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.\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.","description_format":"text","description_chars":6698,"description_truncated":false,"requirements":{"experience_years_min":12,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":true},"security_clearance":false,"languages":[{"language":"English","level":"All levels","optional":false}]},"benefits":["Health insurance"],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology","Prescription Drugs","Biologics & Biosimilars","Generic Drugs"],"lifecycle":[{"event":"open","at":"2026-11-07T20:15:27Z"}],"visa":[],"liveness":{"score":90,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.903,"p_room":1,"age_days":4,"expected_fill_days":52,"reasons":["conf:5","velocity","win:early","comp:brand"],"computed_at":"2026-11-10T06:52:35Z"},"pay":null,"html_url":"https://alion.io/job/teva-assoc-dir-regulatory-affairs","json_url":"https://alion.io/job/teva-assoc-dir-regulatory-affairs.json","meta":{"generated_at":"2026-11-10T21:54:38Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":372,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-11T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.1,"usd":0.01,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":1822915},"rest":"https://alion.io/mcp/rest/get_company?id=1822915"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fteva-assoc-dir-regulatory-affairs"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":2,"usd":0.2},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fteva-assoc-dir-regulatory-affairs"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.1,"usd":0.01},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fteva-assoc-dir-regulatory-affairs"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/teva-assoc-dir-regulatory-affairs\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fteva-assoc-dir-regulatory-affairs"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3927030}},{"tool":"search_jobs","arguments":{"company":"teva.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3927030},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. Docs: https://alion.io/developers"}}