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Director Major Pharmaceuticals Jobs (NOW HIRING)

Role Overview The Senior Director, Sales - Large Pharma US, Clinical & Patient Technology is ... Established senior-level and executive relationships within major pharmaceutical organizations.

Role Overview The Senior Director, Sales - Large Pharma US, Clinical & Patient Technology is ... Established senior-level and executive relationships within major pharmaceutical organizations.

Role Overview The Senior Director, Sales - Large Pharma US, Clinical & Patient Technology is ... Established senior-level and executive relationships within major pharmaceutical organizations.

Role Overview The Senior Director, Sales - Large Pharma US, Clinical & Patient Technology is ... Established senior-level and executive relationships within major pharmaceutical organizations.

Role Overview The Senior Director, Sales - Large Pharma US, Clinical & Patient Technology is ... Established senior-level and executive relationships within major pharmaceutical organizations.

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Director Major Pharmaceuticals information

What does a director in major pharmaceuticals do?

A Director in Major Pharmaceuticals oversees key operations within a pharmaceutical company, such as research and development, regulatory affairs, manufacturing, or marketing. They are responsible for setting strategic goals, ensuring compliance with industry regulations, managing budgets, and leading cross-functional teams. Their role is crucial in bringing new drugs to market, optimizing processes, and driving business growth while maintaining high standards of quality and safety.

What are some common challenges faced by a director in major pharmaceuticals, and how can they navigate these effectively?

Directors in major pharmaceutical companies often face challenges such as balancing regulatory compliance with innovation, managing cross-functional teams, and keeping projects on timeline amid shifting priorities. Navigating these successfully requires strong leadership, the ability to collaborate with R&D, regulatory, and commercial teams, and proactive communication skills. Staying current on industry regulations and fostering a culture of transparency and adaptability can help address these challenges and ensure project success.

What are the key skills and qualifications needed to thrive as a director in major pharmaceuticals, and why are they important?

To thrive as a Director in Major Pharmaceuticals, you need a deep understanding of drug development, regulatory compliance, and business strategy, typically supported by an advanced degree in pharmacy, life sciences, or business administration. Familiarity with regulatory systems (such as FDA, EMA), clinical trial management software, and pharmaceutical quality standards is essential. Exceptional leadership, strategic thinking, and strong communication skills enable effective team management and cross-functional collaboration. These skills and qualifications are crucial for ensuring successful product development, regulatory approval, and organizational growth in a highly regulated industry.

What cities are hiring for Director Major Pharmaceuticals jobs?

Cities with the most Director Major Pharmaceuticals job openings:

What are the most commonly searched types of Major Pharmaceuticals jobs?

The most popular types of Major Pharmaceuticals jobs are:

What states have the most Director Major Pharmaceuticals jobs?

States with the most job openings for Director Major Pharmaceuticals jobs include:

Infographic showing various Director Major Pharmaceuticals job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution.

Senior Project/Program Director (Pharmaceutical - Construction)

Cumming Group

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 days ago


Job description

At Cumming Group, you will work on some of the world's most exciting projects in a dynamic environment where your success is measured by the impact you make. We are one of the fastest-growing project and cost management consultancies in the United States, as reflected in our top 10 rankings in ENR. With over 60 offices globally, an extremely diverse project portfolio, and double-digit year-over-year revenue growth, the opportunities to make your mark are limitless!

The Senior Project Director will serve as the owner's representative for a major pharmaceutical manufacturing capital program in Houston, TX. This role will lead a portfolio of concurrent projects, providing strategic direction and accountability across scope, cost, schedule, safety, quality, risk, and operational readiness. The ideal candidate has led individual project scopes exceeding $100 million and brings deep experience delivering complex pharmaceutical or biotechnology manufacturing facilities. This position requires a consistent on-site presence at the client location.

Essential Duties & Responsibilities:

  • Provide executive oversight for a portfolio of major capital projects and interdependent workstreams.
  • Represent the client's interests throughout design, procurement, construction, commissioning, qualification, start-up, and turnover.
  • Lead Project Directors, Project Managers, consultants, contractors, vendors, and functional project teams.
  • Establish portfolio governance, execution strategies, reporting requirements, decision pathways, and escalation protocols.
  • Integrate project scope, schedules, budgets, risks, resources, and cross-project dependencies into a coordinated execution plan.
  • Maintain accountability for portfolio cost, schedule, safety, quality, and delivery performance.
  • Review project plans, forecasts, schedules, risk registers, change requests, and recovery strategies, intervening when performance is at risk.
  • Lead resolution of significant technical, commercial, contractual, construction, and stakeholder issues.
  • Direct value engineering, constructability, design optimization, and lifecycle-cost initiatives.
  • Ensure project delivery aligns with client standards, manufacturing requirements, GMP expectations, and applicable regulatory and safety requirements.
  • Oversee contracting and procurement strategies, contractor performance, commercial negotiations, claims, and change management.
  • Align engineering, construction, quality, validation, operations, maintenance, and environmental health and safety stakeholders.
  • Provide executive reporting on progress, financial performance, risk exposure, critical decisions, and corrective actions.
  • Ensure facilities and systems are commissioned, qualified, documented, and ready for start-up and operational turnover.
  • Develop and mentor project leadership while driving accountability and consistent execution across the portfolio.

Knowledge & Skills Required:

  • Ability to provide executive oversight across multiple concurrent projects and interdependent workstreams.
  • Strong command of project governance, project controls, integrated scheduling, forecasting, risk management, contingency, and change control.
  • Deep understanding of pharmaceutical facility design, construction, commissioning, qualification, validation, start-up, and operational turnover.
  • Strong commercial and contractual judgment, including procurement strategy, contractor performance, negotiations, claims, and dispute resolution.
  • Working knowledge of GMP, OSHA, environmental, permitting, and process-safety requirements.
  • Ability to align engineering, construction, quality, validation, operations, maintenance, and EHS stakeholders around shared project objectives.
  • Ability to identify emerging issues, make timely decisions, and direct corrective or recovery strategies.
  • Strong executive communication, stakeholder management, negotiation, and team-leadership capabilities.

Preferred Education and Experience:

  • Education: Bachelor's degree in engineering, Construction Management, Architecture, or a related technical discipline.
  • Experience: 15+ years of progressive capital project leadership experience, including:
  • Direct responsibility for individual project scopes exceeding $100 million.
  • Leadership of multiple major projects or workstreams being executed concurrently.
  • Owner's representative or comparable client-side project leadership experience.
  • Delivery of large, complex pharmaceutical or biotechnology manufacturing projects.
  • Experience with API, biologics, fill-finish, advanced manufacturing, laboratory, pilot plant, or similar regulated facilities is preferred.

Preferred Certification: PMP, CCM, PE, or comparable professional credential.

#LI-SJ2

Cumming Group is committed to providing Equal Employment Opportunity in its personnel policies and practices. It is Cumming Group's policy to recruit, hire, train and promote Team Members and applicants for employment without regard to race, color, creed, religion, age, sex, marital status, registered domestic partner status, genetic information, sexual preference, sexual orientation, gender (including gender expression and gender identity), pregnancy (including childbirth or related medical conditions, including breastfeeding), military service, national origin, ancestry, citizenship, physical disability, mental disability, veteran status or any other protected classification under federal, state, or local law. All such decisions are based on (1) individual merit, qualifications, and competence as they relate to the particular position, and (2) promotion of the principle of equal employment opportunity.

All other terms and conditions of employment, such as compensation, benefits, transfers, layoff, return from layoff, training, education, and social and recreational programs, are administered without regard to the characteristics described above. To this end, Cumming Group complies with all provisions of Title VII of the Civil Rights Act of 1964 as amended, all of the rules, regulations and relevant orders of the Secretary of Labor, and all similar state and local laws.

The salary range for this full-time role is $168,300.00-$235,633.37 per year. Ranges are determined based on the position, geography, client and industry experience and level, and represent a good faith effort to provide a fair and equitable salary. This range reflects base salary only, and not the total compensation package. Cumming Group reserves the right to pay more or less than the posted range, depending on a candidate's experience, skills, and qualifications, including client requirements.

In addition to base salary, Cumming Group offers a comprehensive benefits package including:

  • Medical
  • Dental Insurance
  • Vision Insurance
  • 401(k)
  • 401(k) Matching
  • Paid Time Off
  • Paid Holidays
  • Short and long-term disability
  • Employee Assistance Program