Ambio Inc
Job Description
Job Description Salary: $80,000 - $100,000 DOE Primary Responsibilities: Facilitate problem-solving and decision-making with respect to project deliverables and meeting timelines. Facilitates
timelines/tasks/requests
from project teams and other cross-functional departments. Focuses on proactive planning to manage risk, remove barriers, and meet goals. Ensuring smooth transition of project from development phase to commercialization phase. Facilitates meetings and keep them effective by defining concise agenda, acting as a timekeeper, summarizing action items, and maintaining records. Communicates all pre-defined events to team members. Responsible for directing timely execution of the projects and controlling financial aspects to make sure that the project stays within the allocated budget. Maintain accurate record of all correspondence with partners, vendors, contract labs, etc. Create and use Gantt charts, spreadsheets, or other appropriate tools to manage projects. Schedule meetings and teleconferences. Maintain project specific files such as specifications, batch records, formulation development reports, device analysis reports, formulation characterization reports, quotes, POs, etc. Support internal departments when needed. Manage outside and in-house analytical work for various projects. Responsible for making sure that all projects are invoiced timely. Assist in the preparation of the site for customer and regulatory agency inspections.
Qualifications: MS or PhD in pharmaceutical sciences Leadership ability to lead and execute projects Project and Team management skill to optimize resources and deliver results Ability to identify, assess, and manage risk Ability to lead effective problem solving Able to identify issues requiring escalation Excellent organization skills Strong computer operating skills including Microsoft Project/Gantt Charts Detail oriented with multi-tasking abilities and ability to meet deadlines Seeks consensus but makes decisions Self-motivated, able to work in a team and independently In depth knowledge of generic pharmaceutical industry is essential 3+ years experience in pharmaceutical environment and 2+ years experience in project management Experience in Complex Generics and 505 (b) (2) is a PLUS Strong interpersonal and communication skills (written and verbal) for bridging across diverse cross functional, multi-national, geographically dispersed teams
ADA-These Requirements are a Condition of Employment: Must be able to push, pull, squat, stand and walk through-out the day. Prolonged periods sitting at a desk and working on a computer. Must be able to lift 20lbs.
Job Description Salary: $80,000 - $100,000 DOE Primary Responsibilities: Facilitate problem-solving and decision-making with respect to project deliverables and meeting timelines. Facilitates
timelines/tasks/requests
from project teams and other cross-functional departments. Focuses on proactive planning to manage risk, remove barriers, and meet goals. Ensuring smooth transition of project from development phase to commercialization phase. Facilitates meetings and keep them effective by defining concise agenda, acting as a timekeeper, summarizing action items, and maintaining records. Communicates all pre-defined events to team members. Responsible for directing timely execution of the projects and controlling financial aspects to make sure that the project stays within the allocated budget. Maintain accurate record of all correspondence with partners, vendors, contract labs, etc. Create and use Gantt charts, spreadsheets, or other appropriate tools to manage projects. Schedule meetings and teleconferences. Maintain project specific files such as specifications, batch records, formulation development reports, device analysis reports, formulation characterization reports, quotes, POs, etc. Support internal departments when needed. Manage outside and in-house analytical work for various projects. Responsible for making sure that all projects are invoiced timely. Assist in the preparation of the site for customer and regulatory agency inspections.
Qualifications: MS or PhD in pharmaceutical sciences Leadership ability to lead and execute projects Project and Team management skill to optimize resources and deliver results Ability to identify, assess, and manage risk Ability to lead effective problem solving Able to identify issues requiring escalation Excellent organization skills Strong computer operating skills including Microsoft Project/Gantt Charts Detail oriented with multi-tasking abilities and ability to meet deadlines Seeks consensus but makes decisions Self-motivated, able to work in a team and independently In depth knowledge of generic pharmaceutical industry is essential 3+ years experience in pharmaceutical environment and 2+ years experience in project management Experience in Complex Generics and 505 (b) (2) is a PLUS Strong interpersonal and communication skills (written and verbal) for bridging across diverse cross functional, multi-national, geographically dispersed teams
ADA-These Requirements are a Condition of Employment: Must be able to push, pull, squat, stand and walk through-out the day. Prolonged periods sitting at a desk and working on a computer. Must be able to lift 20lbs.