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Company

Original Job Post

Avantor · 1 week ago

Sr. Process Engineer

Ohio, United States

Full-time

Hybrid

Senior Level

7+ years exp

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BiotechnologyElectronics

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Responsibilities

Optimize the Performance Materials organization through process engineering.

Lead engineering projects and deliver innovative solutions in the biopharmaceutical industry.

Work effectively with cross-functional teams and external partners.

Utilize project management methodologies and tools.

Design chemical process and transfer design input for manufacturability.

Collaborate with various teams to deliver process technology solutions.

Implement emerging process technologies to improve performance and efficiency.

Write and review technical documents and lead junior scientists and engineers.

Travel domestically up to 50%.

Qualification

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Biopharmaceutical industryProject managementPMP certificationSchedulingMonitoringManufacturing environmentChemical process designTransfer designManufacturabilityCapital funds request preparationMicrosoft OfficeCommunicationCollaborationProblem-solvingBiopharmaceutical Process DevelopmentQuality by DesignDesign of ExperimentsStatistical Process ControlCross-Functional CollaborationEmerging Process TechnologiesTechnical WritingRegulatory ComplianceTeamworkLeadershipMentoring

Required

BS in Chemical engineering

Experience in engineering, preferably in the biopharmaceutical industry, with a track record of leading engineering projects and delivering innovative solutions

Excellent communication, collaboration, and problem-solving skills, with the ability to work effectively with cross-functional teams, external partners, and senior management

Project management methodologies, tools, and best practices, PMP certification a plus but not required

Planning, scheduling, monitoring, controlling, and reporting project activities and status

Experience in a manufacturing environment, in an engineering capacity involving chemical process design, transfer design input for manufacturability and capital funds request preparation

Collaboration Tools (IE: Microsoft Office)

Preferred

Developing, scaling up, and optimizing process technologies for biopharmaceutical products, such as monoclonal antibodies, recombinant proteins, or vaccines

Applying quality by design (QbD) principles, design of experiments (DOE), and statistical process control (SPC) techniques to process development and validation

Working with cross-functional teams, including R&D, manufacturing, quality, engineering, and regulatory affairs, to deliver process technology solutions that meet business objectives and customer expectations

Evaluating and implementing emerging process technologies, such as continuous manufacturing, single-use systems, advanced analytical tools, or digital transformation, to improve process performance, efficiency, and robustness

Writing and reviewing technical documents, such as protocols, reports, standard operating procedures, risk assessments, and regulatory submissions

Leading and mentoring junior scientists and engineers, as well as collaborating with external partners, such as academic institutions, contract research organizations, or equipment suppliers

MS/PHD in core sciences (Chemistry, Biopharma, Engineering), MBA a plus

PMP certification