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Director Pharmaceutical Development Jobs in Romeoville, IL

R&D Assay Director - Accellix

Lombard, IL · On-site

$195K - $255K/yr

... pharmaceutical, biotech, or medical device regulated environment, including direct experience in ... Development, or Quality Control functions including 5+ years of specific professional Team ...

R&D Assay Director - Accellix

Lombard, IL · On-site

$195K - $255K/yr

... pharmaceutical, biotech, or medical device regulated environment, including direct experience in ... Development, or Quality Control functions including 5+ years of specific professional Team ...

... pharmaceutical, biotech, or medical device regulated environment, including direct experience in ... Development, or Quality Control functions including 5+ years of specific professional Team ...

Pharmacist Full Time

Joliet, IL · On-site

$52 - $56/hr

... development Vision insurance Pharmacist - Full Time - St. Jude Pharmacy, Joliet, IL $52 to $56 per ... Direct access to ownership and a supportive technician team Strong, stable patient base and a ...

We partner with pharmaceutical, biotechnology, and medical device companies across the full product ... Key Responsibilities Leadership & Talent Development * Manage and mentor high-performing teams ...

We partner with pharmaceutical, biotechnology, and medical device companies across the full product ... Key Responsibilities Leadership & Talent Development * Manage and mentor high-performing teams ...

We partner with pharmaceutical, biotechnology, and medical device companies across the full product ... Key Responsibilities Leadership & Talent Development * Manage and mentor high-performing teams ...

Showing results 21-40

Director Pharmaceutical Development information

See Romeoville, IL salary details

$43.8K

$84.2K

$165.2K

How much do director pharmaceutical development jobs pay per year?

As of Aug 16, 2026, the average yearly pay for director pharmaceutical development in Romeoville, IL is $84,218.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,100.00 and $99,400.00 per year, depending on experience, location, and employer.

How does a director pharmaceutical development typically collaborate with cross-functional teams during the drug development process?

A Director of Pharmaceutical Development regularly collaborates with multidisciplinary teams, including research scientists, regulatory affairs, clinical development, and manufacturing departments. This role acts as a bridge to ensure alignment between scientific objectives, regulatory requirements, and commercial goals. Effective communication and project management skills are crucial, as the director must coordinate timelines, resolve technical challenges, and integrate feedback from different stakeholders to advance projects efficiently. Collaboration is key to ensuring that product development stays on track and meets both quality standards and regulatory expectations.

What does a director pharmaceutical development do?

A Director of Pharmaceutical Development leads and oversees the process of developing new pharmaceutical products, from initial concept through to clinical trials and regulatory approval. They manage teams of scientists, coordinate with regulatory agencies, and ensure projects meet timelines, budgets, and quality standards. Additionally, they collaborate with cross-functional departments such as research, manufacturing, and marketing to align product development with business goals. Their role is crucial in bringing safe and effective medications to market.

What are the key skills and qualifications needed to thrive as a director pharmaceutical development, and why are they important?

To thrive as a Director of Pharmaceutical Development, you need advanced expertise in pharmaceutical sciences, drug development processes, and regulatory compliance, typically supported by a PhD or PharmD and significant industry experience. Familiarity with tools like LIMS, project management software, and knowledge of FDA/EMA submission systems is crucial. Outstanding leadership, strategic thinking, and cross-functional communication skills distinguish top performers in this role. These competencies ensure effective management of complex development pipelines, regulatory success, and alignment with organizational goals.

What is the difference between Director Pharmaceutical Development vs Senior Pharmaceutical Scientist?

AspectDirector Pharmaceutical DevelopmentSenior Pharmaceutical Scientist
CredentialsAdvanced degrees (PhD, PharmD), extensive industry experienceMaster's or PhD in pharmaceutical sciences or related field
Work EnvironmentLeadership roles, strategic planning, cross-department collaborationResearch, formulation, laboratory work
Employer & Industry UsagePharmaceutical companies, biotech firms, R&D divisionsResearch labs, development teams within pharma companies

The main difference is that the Director Pharmaceutical Development oversees strategic development projects and manages teams, while the Senior Pharmaceutical Scientist focuses on hands-on research and formulation work. The director role involves leadership and planning, whereas the senior scientist role emphasizes technical expertise and experimentation.

What cities near Romeoville, IL are hiring for Director Pharmaceutical Development jobs?

Cities near Romeoville, IL with the most Director Pharmaceutical Development job openings:

Director of Client Development - DesignBuild & EPC Capital Projects (Life Sciences)

Paper Converting Machine

Chicago, IL

Full-time

Re-posted 4 days ago


Job description

About Us:

BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.


 

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.


 

Job Description:

Who You'll Work With

You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a worldclass professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.
When you join BW Design Group as a Director, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world's leading companies solve their most difficult problems. You will join our Architecture + Engineering + Construction (AEC) Business and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.

Role Overview

We are seeking a Director, Client Development - Life Sciences Manufacturing (DesignBuild / EPC) to build, secure, and execute largescale capital programs ($100M+), with direct accountability for bookings, commercial strategy, and delivery outcomes. This clientfacing growth leadership role blends strategic client alignment with deep technical expertise to expand multiproject initiatives across pharmaceutical, biotech, medical device, and advanced therapy manufacturing environments-including cGMP facilities, utilities, laboratories, and controlled manufacturing spaces-in both brownfield and greenfield settings.

Operating outside traditional utilization expectations (e.g., billable hours), the role is measured by bookings, marginaware account growth, delivery performance, and longterm client value-empowering you to focus on highimpact client strategy, pursuit leadership, and capital alignment in an entrepreneurial environment. Dedicated preconstruction, engineering, and construction teams support the role, ensuring technical depth and delivery leadership partnership complement your accountability in client development. Success in this role is defined by secured bookings, profitable delivery of multiproject capital programs, and sustained executivelevel client relationships. Programs may span smallmolecule, biologics, advanced therapies, and medical device manufacturing, requiring flexible delivery strategies across diverse regulated environments.

What You'll Do

  • Own bookings targets, pricing strategy, and commercial positioning, developing opportunities into secured designbuild (DB) and engineerprocureconstruct (EPC) initiatives supporting life sciences manufacturing, laboratory, clean utility, and distribution facilities, including validationready environments-leveraging your technical insights to achieve outcomes.

  • Engage client executive stakeholders across Engineering, Manufacturing, Quality, Validation, Operations, Supply Chain, Finance, and Environmental, Health, and Safety (EHS) to align capital investment with capacity growth, regulatory compliance, operational readiness, and speedtomarket objectives.

  • Lead pursuit strategy and executive presentations; negotiate commercial terms, delivery approach, pricing, and risk allocation with direct accountability for contractual outcomes, drawing on technical expertise to build client trust.

  • Lead internal subject matter experts (SMEs) across process, architecture/engineering (A/E), preconstruction, construction, and controls to deliver integrated DB/EPC solutions.

  • Participate in go/nogo reviews, pipeline governance, forecasting, and customer relationship management (CRM) discipline to support predictable growth and backlog health.

  • Serve as executive sponsor through execution and closeout, remaining accountable for client satisfaction, commercial performance, and longterm account profitability.

What You'll Bring

  • 15+ years leading and delivering capital programs for manufacturing clients in a designbuild, EPC, or integrated A/E/C environment-particularly within life sciences, pharmaceutical, biotech, medical device, or other regulated production environments-with personal responsibility for securing work, pricing, and delivery execution.

  • Deep understanding of life sciences manufacturing operations, including cGMP production, people and material flows, cleanroom classifications and pressure cascades, adjacency planning, clean utilities (WFI, PW, clean steam), automation, validation readiness, and operational turnover across manufacturing and support systems.

  • Experience leading large, multidisciplinary delivery teams with authority over scope, cost, schedule, and margin.

  • This role requires ownership of commercial outcomes and delivery risk within a DB/EPC model, using technical expertise to secure and execute highvalue contracts.

  • Use industry experience and technical knowledge in delivery strategy development and cost/schedule derisking, including preconstruction, constructability, phasing, shutdown/tiein planning, commissioning, qualification, and validation (CQV) readiness, operational readiness and turnover (ORAT), and risk management -all to support client pursuits and marginaware growth.

  • Life sciences manufacturing sector experience is strongly preferred; pharmaceutical, biotech, cell & gene therapy, or medical device manufacturing experience applicable.

  • Experience working in qualitydriven and regulated environments; cGMPregulated facilities, FDA/EMA oversight, and validation exposure required.

  • Executivelevel communication skills with the ability to influence and align technical and nontechnical stakeholders.

  • Willingness to travel for client engagement, site walkdowns, and industry events.

  • BS or MS in Engineering, Architecture, Construction Management, or related field.

  • Professional Engineer (PE) preferred but not required; Master of Business Administration (MBA) and/or Project Management Professional (PMP) a plus.

Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Director, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a worldclass engineer and a highly effective leader.
Feel like you're on the path to becoming a Director but you're not quite there yet? We'd love to connect with you to see if we can take you from where you are today and grow you into a BW Design Group Consultant.

#LI-BH1


 

At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.


 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.


Company:

Design Group