Senior Project Manager - Biopharmaceuticals

Prior experience in the pharmaceutical or biotech industry is required for this position. MMR Consulting is a prominent engineering and consulting firm dedicated to advancing the pharmaceutical and biotechnology sectors in the US and Canada. We offer a range of services including Engineering, Project Management, and Consulting. Our engineering expertise spans Process, Automation, and Facilities, while our pharmaceutical knowledge encompasses Oral Solid Dosage, Semi-Solids, Liquid-Dosage (both TS and Aseptic), API manufacturing, and Biotechnology, including Vaccines, Monoclonal Antibodies, Cell & Gene Therapy, and mRNA technologies. Join our dynamic team where you will collaborate with skilled engineers engaged in the design, commissioning, and qualification of various processes and facilities. This role involves working directly at client sites, primarily located in the Bradley, IL area (1.5 hrs. drive from Chicago). Key Responsibilities Provide expert technical guidance on engineering assessments, project management, design, commissioning, and start-up of facilities and equipment for projects including upgrades, renovations, and expansions. Lead or assist in project execution from feasibility through to completion, encompassing all project phases: Feasibility Assessments Concept Design, Basic Design, Detailed Design Procurement Construction / Installation Project Controls and Monitoring Commissioning & Qualification Prepare comprehensive business cases, outlining project purposes, risks, budgets, schedules, and resource requirements. Effectively manage relationships with other engineering firms, equipment vendors, construction companies, and internal/external stakeholders to drive project success. Oversee Capital Projects and review technical documentation, including P&IDs, specifications, layouts, manuals, and datasheets. Embed safety practices into all project aspects (HAZOP reviews, PHSRs, and design review sessions with EHS representatives). Prepare and review automation sequences as necessary for Process Automation. Coordinate across various engineering disciplines and departments (Process, Automation, Facilities, Procurement, Construction Management, Commissioning, Qualification & Validation, Manufacturing, EHS, Quality & Compliance). Utilize project management tools to streamline project execution, including procurement tracking, vendor management, and risk register logs. Organize and lead meetings with cross-functional teams to expedite project progress, facilitate decision-making, and provide updates. Occasional travel may be required for vendor meetings or Factory Acceptance Testing (FATs). Support during critical phases such as construction and commissioning may require extended hours or shutdown coverage. Engage in client management to maintain key relationships and support business development initiatives. Conduct site visits while adhering to safety protocols, including wearing necessary PPE. Supervise contractors during the critical installation of process equipment and related utilities. Perform additional tasks as assigned by client or MMR based on project needs. This role involves compliance with client safety regulations, including any applicable COVID-19 vaccination protocols. Qualifications Over 10 years of engineering or project management experience in the pharmaceutical or biotech industry, with proficiency in cGMP operations. Capital project management experience is essential. Demonstrated leadership ability to drive complex projects involving multiple stakeholders. Mentorship skills to support and develop junior and mid-level team members. Basic proficiency in AutoCAD is preferred. Bachelor's degree in Mechanical, Chemical, or Electrical Engineering is required. Project Management certification is highly advantageous. Willingness to travel as necessary, particularly to the US. Contact us to apply: recruitment@mmrengineering.com Salary range: $70,000 - $120,000 based on experience. Equal Employment Opportunity and Reasonable Accommodations MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are dedicated to providing reasonable accommodations to individuals with disabilities globally. If you require a reasonable accommodation due to a medical condition or disability during the application or interview process, please let us know.