
201 - 500 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syner-G BioPharma Group is the world's leading provider of chemistry, manufacturing and controls (CMC), regulatory affairs, and medical writing solutions for the biopharma sector. They offer comprehensive services that navigate clients through the complexities of pharmaceutical development, regulatory submissions, and quality compliance, ensuring high-quality outcomes. With a multidisciplinary team, Syner-G integrates science, engineering, and regulatory expertise to support drug development from pre-IND to post-approval phases, enabling timely submissions and patient safety adherence.
🕒 May 20
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201 - 500 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syner-G BioPharma Group is the world's leading provider of chemistry, manufacturing and controls (CMC), regulatory affairs, and medical writing solutions for the biopharma sector. They offer comprehensive services that navigate clients through the complexities of pharmaceutical development, regulatory submissions, and quality compliance, ensuring high-quality outcomes. With a multidisciplinary team, Syner-G integrates science, engineering, and regulatory expertise to support drug development from pre-IND to post-approval phases, enabling timely submissions and patient safety adherence.
• Define project goals, scope, objectives, and deliverables in alignment with client requirements. • Lead and motivate project teams, ensuring clear communication, collaboration, and accountability. • Allocate resources effectively, manage project budgets, and monitor expenses to ensure costeffectiveness. • Identify potential risks and issues, develop mitigation strategies, and proactively address challenges to minimize project disruptions. • Maintain strong relationships with clients, vendors, and internal stakeholders, managing expectations and providing regular updates on project progress. • Ensure adherence to quality standards, review project documentation, and facilitate audits to maintain compliance with regulatory requirements. • Oversee the movement of materials, manage labeling processes, and ensure timely delivery of clinical supplies to support trial activities. • Drive process improvements, implement best practices, and seek opportunities to enhance project efficiency and effectiveness. • Prepare comprehensive project reports, documentation, and presentations for internal and external stakeholders.
• Bachelor's degree in science or related field; project management certification (PMP) preferred. • Proven experience in project management, preferably in the pharmaceutical or life sciences industry. • Proficiency in project management tools and software. • Superb leadership, communication, and interpersonal skills. • Excellent organizational and problem-solving abilities. • Knowledge of clinical supply operations and regulatory requirements. • Ability to work effectively in a fast-paced, dynamic environment. • Strong skills in teamwork and collaboration, adaptability and flexibility, initiative and confidence, prioritization, influencing others, critical thinking, and technical tasks proficiency.
• Health insurance • 401(k) matching • Flexible working hours • Paid time off • Remote work options • Professional development opportunities • Generous flexible paid time off program • Company paid holidays
Apply Now🕒 May 20
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