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Tier-1 employer and mid-level seniority increase competition, but MES/pharma specialization narrows qualified applicant pool.
Role requires MES, pharma-regulatory and manufacturing domain knowledge, making cross-industry transfers difficult.
Mandatory 5+ years and MES/regulatory experience create strict filters for candidate shortlisting.
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Manage end-to-end business analysis workstreams independently, addressing complex and ambiguous business problems within Pharma Technical Operations Manufacturing Technologies.
Lead requirements gathering, root cause analysis, and contribute to solution selection ensuring strategic alignment and demonstrable business value.
Act as a trusted advisor to cross-functional stakeholders, facilitating workshops, resolving conflicts, mentoring junior analysts, and shaping team methodologies and best practices.
Master’s degree in Engineering, Computer Science, or related technical field.
Minimum 5 years of Business Analysis/Consultancy experience in life sciences, medical, or pharmaceutical sectors in regulated environments.
At least 5 years experience working with Manufacturing Execution Systems, preferably Rockwell PharmaSuite.
Work Experience Required: 5+ years managing end-to-end BA workstreams with demonstrated expertise in MES within regulated environments.
Experienced in managing complex business analysis in pharmaceutical manufacturing, specifically with MES and recipe management in regulated environments.
Strong strategic orientation capable of translating requirements into implementation plans and long-term solution roadmaps.
Proficient in stakeholder management across diverse functions with skills in conflict resolution and mentoring junior analysts.