About the Role
Our client, a globally respected pharmaceutical company, is seeking a highly motivated and experienced Senior Pharmaceutical Project Manager to lead key initiatives from their **Vereeniging, Gauteng, ZA** office. This role is pivotal in overseeing the successful execution of complex projects, from drug development and clinical trials to manufacturing scale-up and regulatory submissions. The ideal candidate will possess a strong understanding of the pharmaceutical lifecycle, exceptional leadership skills, and a proven ability to manage cross-functional teams and timelines effectively. This on-site position requires a dedicated professional committed to driving project success and ensuring the timely delivery of critical pharmaceutical advancements within the **Vereeniging** region.
Key Responsibilities
- Lead and manage the planning, execution, and closure of pharmaceutical projects, ensuring they are completed on time, within scope, and within budget.
- Develop comprehensive project plans, defining objectives, deliverables, milestones, resource requirements, and risk mitigation strategies.
- Coordinate and collaborate with cross-functional teams, including R&D, Clinical Operations, Regulatory Affairs, Manufacturing, and Quality Assurance.
- Manage project budgets, track expenditures, and provide regular financial reports.
- Identify potential project risks and issues, and develop proactive strategies to address them.
- Communicate project status, progress, and key decisions to stakeholders, including senior management, through regular reports and presentations.
- Ensure compliance with all relevant regulatory guidelines (e.g., GMP, ICH) and company policies throughout the project lifecycle.
- Facilitate project meetings, ensuring clear agendas, action items, and follow-up.
- Mentor and guide project team members, fostering a collaborative and high-performance work environment.
- Manage vendor and external partner relationships as required for project success.
Requirements
- Bachelor's degree in Pharmacy, Science, Engineering, Business, or a related field.
- A Master's degree or PMP certification is highly desirable.
- A minimum of 7 years of experience in project management, with at least 5 years specifically within the pharmaceutical or biotechnology industry.
- Proven track record of successfully managing complex pharmaceutical projects from initiation to completion.
- In-depth understanding of the drug development process, clinical trials, and pharmaceutical manufacturing.
- Strong knowledge of regulatory requirements (e.g., FDA, EMA, SAHPRA).
- Excellent leadership, communication, negotiation, and interpersonal skills.
- Proficiency in project management software (e.g., MS Project, Jira).
- Strong analytical, problem-solving, and risk management abilities.
- Ability to manage multiple projects simultaneously and prioritize effectively.
Benefits
- Our client offers a highly competitive salary package, along with performance-based bonuses and potential for long-term incentives.
- Comprehensive health, dental, and vision insurance are provided.
- A generous retirement savings plan with employer match is available.
- This on-site role offers stability and the opportunity to lead impactful projects.
- Continuous professional development, training opportunities, and career advancement within a leading pharmaceutical organization are key.
- Paid time off and company holidays are provided.
- Join a team dedicated to advancing healthcare.