- 経験
- 12–18 yrs
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 1時間前
- 作業モード
- 在任中
- 教育
- 卒業生であれば誰でも
- 資格
- Candidates having any graduate degree are eligible to apply.
- 再開する
- 応募必須
勤務地
仕事内容
Role Overview
This position involves leading application management services (AMS) assessments, designing solutions, supporting proposals, and ensuring delivery quality within the Life Sciences domain.
Key Responsibilities
- Analyze portfolios and conduct workshops for solution development.
- Create solution designs and estimation models.
- Evaluate vendors and rationalize applications.
- Manage stakeholders and develop transformation roadmaps.
Domain & Platforms
Expertise spans Pharma R&D, Labs, Clinical, Manufacturing, Quality, Regulatory, TechOps, Commercial, and enterprise integrations.
Mandatory knowledge in platforms including Discovery, Preclinical, Lab Informatics, ELN, LIMS, GeneData, Benchling, BIOVIA, and Revvity.
Proposal Responsibilities
- Assess application inventories and map criticality.
- Define support models and plan transitions.
- Estimate efforts with SLA/KPI frameworks.
- Recommend modernizations and assess risks.
Regulatory & Compliance
- Understand and ensure adherence to GxP, GAMP5, 21 CFR Part 11, Annex 11.
- Maintain data integrity, computer system validation (CSV), audit readiness, and validation lifecycle awareness.
Qualifications & Skills
- Bachelor's or Master's degree in Engineering, Pharmacy, Biotechnology, Life Sciences, or equivalent.
- Substantial Pharma domain experience with excellent stakeholder communication.
- Preferred: global delivery experience, Agile/SAFe methodologies, cloud platforms, AI/Data knowledge, and related platform certifications.
スキル
ステークホルダーとのコミュニケーション
ベンダー評価
Cloud Technologies
AI and data analytics
Pharma R&D domain expertise
Application management services (AMS)
Pharma platforms (LIMS, ELN, BIOVIA, Revvity)
Regulatory compliance (GxP, GAMP5, 21 CFR Part 11)
Solution design and estimation
Transformation roadmap development
Agile/SAFe methodologies