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Pharmaceutical Sales jobs in Hyderabad, Telangana

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    • Lead and manage end-to-end regulatory activities predominantly for US ANDA submissions and post-approval lifecycle management for complex sterile dosage forms.
    • View all AVEVA DRUG DELIVERY SYSTEMS INC jobs - Kukatpally, Hyderabad, Telangana jobs - Team Leader jobs in Kukatpally, Hyderabad, Telangana
    • Salary Search: Team Leader, RA salaries in Kukatpally, Hyderabad, Telangana
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    • Effective Promotion of company’s products to achieve the Sales Budgets assigned to your.
    •  Implementing market & business strategy designed by the management.
    • May direct the work of other lower level sales professionals or manage sales processes and / or accounts involving multiple team members.
    • Relevant experience in pharmaceutical sales/marketing.
    • Revenue growth and sales targets.
    • Experience: 5 years in pharma sales / marketing / business…
    • Project Management for both internal and client projects.
    • Implement project management tools and methodologies to track the project progress and identify…
  • Job Description: * ales & Marketing * Communication Skills * Customer Relationship Management * Time Management * Territory Management * Product Knowledge *…
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    • Experience* : 0 to 6 Months( Fresher can also apply).
    • It's a field job.*.
    • Job Types: Full-time, Permanent, Fresher.
    • Freshers or candidates with experience in pharmaceutical sales can apply.
    • Basic knowledge of pharmaceutical products and medical terminology.
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    • Candidate Profile Experience in pharmaceutical sales; prior First Line Management experience preferred.
    • Maintain and monitor primary & secondary sales records.
    • Drive sales of medical capital equipment across government hospitals and institutions.
    • Achieve sales targets while providing regular market intelligence and…
    • Achieving assigned primary sales targets and expanding market coverage.
    • Onboarding Distributors under the appointed Super Stockist.
    • Generate prescriptions and achieve sales targets product-wise, value-wise both in primary and secondary sales on monthly as well as yearly basis.
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    • Be responsible for receiving and checking all deliveries.
    • Ensure all stock is stored in the correct manner.
    • Keep a record of and report any frequent shortages…
    • Build a performance-driven and compliant sales culture.
    • Maintain business hygiene by reducing sales returns and minimizing expiries.
    • Build a performance-driven and compliant sales culture.
    • Maintain business hygiene by reducing sales returns and minimizing expiries.

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Job Post Details

Team Leader, RA - job post

AVEVA DRUG DELIVERY SYSTEMS INC
3.7 out of 5 stars
Kukatpally, Hyderabad, Telangana
₹13,00,000 - ₹20,00,000 a month
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Job details

Pay

  • ₹13,00,000 - ₹20,00,000 a month

Location

Kukatpally, Hyderabad, Telangana

Full job description

  • Lead and manage end-to-end regulatory activities predominantly for US ANDA submissions and post-approval lifecycle management for complex sterile dosage forms.
  • Guide and supervise a team of 4–5 senior regulatory associates, providing strategic direction, mentoring, and performance oversight.
  • Act as a regulatory lead in cross-functional teams (CFTs) involving R&D, QA, QC, AR&D, Formulation, and Project Management to resolve regulatory deficiencies and plan responses.
  • Strategize and draft FDA deficiency responses, ensuring alignment with regulatory expectations and internal timelines.
  • Liaise with R&D for preparing controlled correspondences, pre-submission meetings and teleconferences packages, as needed.
  • Ensure timely and compliant filing of supplements (PAS, CBE-30, CBE-0), annual reports, and amendments.
  • Monitor and interpret evolving FDA regulations and guidances; assess impact and implement regulatory strategy changes accordingly.
  • Represent Regulatory Affairs in partner meetings and contribute to regulatory planning and communication with external stakeholders and business partners.
  • Review and approve critical CMC documentation, bridging technical content with regulatory requirements.
  • Drive continuous improvement in regulatory processes, systems, and team capabilities.
  • 15+ years of experience in US Regulatory Affairs with a strong focus on sterile injectable products and complex generics.
  • Proven experience with microsphere formulations, peptides, BFS, nasal sprays, ophthalmics, ointments, and other sterile/non-oral dosage forms.
  • In-depth knowledge of US FDA regulations, eCTD submissions, and FDA communication pathways.
  • Hands-on experience in handling FDA queries, CRLs, and working closely with CFTs to compile timely and high-quality responses.
  • Strong leadership, project management, and cross-functional collaboration skills.
  • Excellent communication, analytical, and problem-solving abilities.
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