





Tier-1 employer, mid-level program role, metro location, and generalist requirements increase applicant competition.
Requires pharmaceutical/life-sciences regulatory and GMP expertise, making cross-industry transfers less transferable.
Explicit 2+ years, industry-specific GMP/regulatory requirements and preferred PMP increase filtering.
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Coordinate and manage complex cross-functional programs from initiation to delivery ensuring alignment with business objectives and customer needs.
Manage program scope, schedule, and budget within a dynamic matrix environment with internal and external stakeholders.
Drive decision-making, maintain program control, and deliver results supporting the mission of enabling healthier, cleaner, and safer outcomes.
Advanced degree in Engineering, Life Sciences, Chemistry, Business Administration, or related field.
Minimum 2 years of program/project management experience in pharmaceutical, biotechnology, or life sciences industry.
Strong knowledge of GMP, quality systems, and regulatory requirements in pharmaceutical manufacturing.
English proficiency required; PMP or equivalent certification preferred; 10-15% travel may be required.
Experienced program manager with demonstrated success coordinating cross-functional teams in matrix organizations within life sciences/pharmaceutical sectors.
Strong financial acumen with budget management and forecasting experience, and advanced proficiency in project management tools.
Detail-oriented, proactive risk manager with strong stakeholder engagement skills and a data-driven approach to decision-making.