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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 ...

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 ...

As an independent commercial solutions partner to pharmaceutical and life science companies, we ... The depth of the position demands qualifications developed over a minimum of 7 years of related ...

Showing results 41-60

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 Sep 6, 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.

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.

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 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.

How to become a director pharmaceutical development?

To become a director of pharmaceutical development, candidates typically need a doctoral degree in a related field such as pharmacy, chemistry, or biology, along with extensive experience in drug development and regulatory processes. Strong leadership, project management skills, and knowledge of Good Manufacturing Practices (GMP) are essential. Progression often involves advancing through roles like senior scientist or manager before reaching a director level.

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, Compounding Operations - Romeoville, Illinois

Ro

Romeoville, IL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago


Job description

Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 99% of primary care deserts.
Ro is consistently recognized as a top workplace in Health Care, in New York, and for Women and Parents-earning more than 20 honors from Fortune, Great Place to Work, and PEOPLE since 2021. In 2025 alone, we ranked top 5 among medium workplaces in Health Care and New York, and top 50 nationwide.
The Director, Compounding Operations is the enterprise owner of compounding operations across Ro's pharmacy network. This role is accountable for operational execution, quality, compliance, performance, inspection readiness, and scalable growth across both sterile and non-sterile compounding operations.
Reporting directly to the VP of Compounding & Manufacturing, this leader oversees Lead Compounding Pharmacists across all current and future facilities, including Illinois and Florida. Site-level Lead Compounding Pharmacists and Pharmacists-in-Charge are responsible for local execution, while the Director defines the enterprise operating model, standards, systems, metrics, escalation pathways, and accountability framework required to drive consistent performance across the network. All compounding personnel align indirectly to this role through the site leadership structure.
This is a hands-on enterprise leadership position requiring strong operational discipline, quality oversight, regulatory judgment, and the ability to build and scale controlled compounding operations. The role ensures that practices are standardized, documented, and aligned with USP <795>, <797>, and <800> across all sites.
The Director partners closely with Pharmacists-in-Charge, Quality, Compliance, Operations, Legal, Product, and Supply Chain while maintaining clear accountability for cross-site consistency, performance management, operational controls, and escalation of compounding-related risks.
This leader is ultimately accountable for the systems and controls that support finished-product quality, release readiness, inspection readiness, and overall compounding performance across Ro's pharmacy network.
The role is based on-site in Romeoville, Illinois, with travel to other compounding locations as needed.
What You'll Do
  • Lead end-to-end compounding operations across all sites, ensuring consistent execution, operational efficiency, and full regulatory compliance.
  • Serve as the subject matter expert for USP <795>, <797>, and <800>, maintaining continuous inspection readiness and leading internal, Board of Pharmacy, and regulatory audits.
  • Standardize and continuously improve compounding workflows, batch records, documentation practices, policies and procedures, and training programs across all sites.
  • Establish and enforce rigorous batch record review and verification processes across technicians, pharmacists, and Quality Assurance.
  • Lead deviation investigations and corrective and preventive actions in partnership with the Quality team, serving as the escalation point for compounding and quality-related issues.
  • Partner with Pharmacists-in-Charge and site leadership to strengthen daily execution, accountability, and performance across facilities.
  • Define, monitor, and improve key operational and quality metrics, including deviations, right-first-time performance, and throughput.
  • Produce high-quality, data-driven reports on compounding strategy, operations, quality, and compliance.
  • Ensure the qualification, maintenance, and ongoing compliance of compounding equipment and facilities.
  • Collaborate cross-functionally with Quality, Compliance, Legal, and Product teams to support operational initiatives and new product introductions.
  • Support the hiring, training, and professional development of compounding pharmacists and technicians.
  • Build and sustain a culture of compliance, uncompromising safety, accountability, and operational excellence.

What You'll Bring to the Team
  • Minimum of 5 years of experience in pharmacy compounding operations, with demonstrated expertise in both sterile and nonsterile compounding.
  • Advanced working knowledge of USP <795>, <797>, and <800>, including experience supporting regulatory inspections and internal and external audits.
  • At least 2 years of leadership experience managing pharmacists, pharmacy technicians, or compounding operations teams.
  • Deep, hands-on expertise in sterile and nonsterile compounding environments, including workflows, equipment, documentation, and operational controls.
  • Demonstrated experience partnering with Quality and Compliance teams in a regulated healthcare environment to implement and sustain compounding quality and compliance standards.

Preferred Qualifications
  • Doctor of Pharmacy (PharmD) degree from an accredited college or school of pharmacy preferred.
  • Active, unrestricted pharmacist license in good standing; licensure in multiple states preferred.
  • Strong operational judgment, with the ability to maintain rigorous compliance standards while improving efficiency and execution.
  • Ability to operate independently, make sound decisions, and drive alignment across cross-functional stakeholders.
  • Demonstrated effectiveness in a fast-paced, high-growth, and evolving operational environment.
  • Willingness and ability to travel up to 30%.

We've Got You Covered:
  • Full medical, dental, and vision insurance + OneMedical membership
  • Healthcare and Dependent Care FSA
  • 401(k) with company match
  • Flexible PTO
  • Wellbeing + Learning & Growth stipends
  • Paid parental leave + Fertility benefits
  • Pet insurance
  • Student loan refinancing
  • Virtual resources for mindfulness, counseling, and fitness

We welcome qualified candidates of all races, creeds, genders, and sexuality to apply.
The target base salary for this position ranges from $175,500 to $206,500, in addition to a competitive equity and benefits package (as applicable). When determining compensation, we analyze and carefully consider several factors, including location, job-related knowledge, skills and experience. These considerations may cause your compensation to vary.
At Ro, we believe that our diverse perspectives are our biggest strengths - and that embracing them will create real change in healthcare. As an equal opportunity employer, we provide equal opportunity in all aspects of employment, including recruiting, hiring, compensation, training and promotion, termination, and any other terms and conditions of employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, familial status, age, disability and/or any other legally protected classification protected by federal, state, or local law.
Ro is committed to providing reasonable accommodations for qualified individuals with disabilities in our application and interview process. If you require a reasonable accommodation in the application or interview process, please contact us at [email protected].
See our California Privacy Policy here.
We may use automated tools, including artificial intelligence (AI), to assist with parts of our recruiting and hiring process, such as reviewing applications, evaluating resumes, and assessing responses or job-related qualifications. These tools are used to support our recruitment team and do not replace human judgment. Final hiring decisions are made by humans.