The Company – Syner-G Pharma Consulting, LLC:

  • A young, dynamic, entrepreneurial and growing regulatory and technical consulting firm providing specialized consulting and contracting services in the areas of Chemistry, Manufacturing and Controls (CMC) for biopharmaceutical companies (small molecule and biologic products)
  • Adept in developing risk-based CMC strategies in accordance with cGMP for 21st Century initiatives and Quality by Design (QbD) principles
  • Distinguish ourselves by our passion for creativity and innovation
  • Offer flexible work environment allows for on-site, off-site and virtual-office scenarios
  • Clients include national and multinational pharmaceutical companies

The Candidate:

  • An aspiring science professional driven by learning and applying scientific principles to solve CMC technical and project management challenges
  • A hands-on Project Coordinator with a strong understanding of the pharma industry to assist in the planning and coordination of external client projects.
  • The client-facing position contributes to the company’s success by facilitating efficient and focused project team planning and coordination
  • The position will play a key role maintaining coordination and communication between internal departments and its customers.
  • The individual will develop cross-functional expertise and will have the opportunity to gain significant exposure to many aspects of the business.
  • Has a passion to help patients by enabling the expeditious development and approval of high-quality, life-saving medicines
  • Has a BS or MS in biochemistry, chemistry, molecular biology, chemical or bio engineering fields with atleast 2-3 years of industry experience in pharma/biopharma settings
  • Familiar with FDA, ICH and other relevant CMC/Quality and cGMP guidance documents is a place
  • An “outside the box thinker” who is not limited by dogmas but have a passion for applying current scientific and technical principles to design innovative strategies and solve technical CMC challenges
  • Should be diligent in paying attention to details and take pride in delivering high quality output within defined timelines
  • Should be fluent in MS Office (Word/Excel/PowerPoint/Project) suite of products and familiar with CMC documentation as well as experienced in the use of Gantt charts
  • A great team player with leadership qualities to work with cross-functional teams
  • Has excellent written and verbal communication skills
  • Additional desired qualification/experience: Graduate degree is a plus

Critical success factors:

  • Likes working in entrepreneurial settings and takes responsibility and ownership for the deliverables
  • Independent thinker and self-motivated
  • Enjoys learning and applying problem solving skills in a fast-paced setting
  • A sense of urgency and appreciation for the expedited development of life-saving medicines
  • Strong appreciation for science-based CMC development
  • Comfortable with multitasking and making decision and progress under ambiguous scenarios
  • Comfortable and confident in presenting ideas to large audiences and in smaller client settings.
  • Understanding of client needs for continuous improvement
  • Understanding of regulatory, technical and quality
Job Category: Project Manager
Job Type: Full Time

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