Center For Pharmaceutical Science And Technology Work Values

Daily Duties at Center For Pharmaceutical Science And Technology:

Performed initial and time-point stability analysis of samples for Phase I and II clinical trials. Qualified analytical assays including the writing of qualification reports and standard operating procedures. Supported manufacturing activities of various formulations for Phase I and II clinical trials

What they like about Center For Pharmaceutical Science And Technology:

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

Tags

Formulation development, Project management, cGMP training, Standard operating procedures, Data and document review, Shipping/cold chain logistics, Product scale-up, Technology transfer

Skills

Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts., Sales Support, Software Implementation, Requirements Analysis & Specification, Leadership , Chemistry Manufacturing Control – directed formulation/process design, scale-up, technology transfer, manufacturing and process/analytical method validation; cleanroom manufacturing. , Project Management – managed activities and optimal performance of internal cross- functional project teams and external groups of clients, analytical outsourcing and shipping logistics (including cold chain). , Quality – executed project success from quality by design for GLP/GMP conformance., Regulatory – contributed as effective team member for clients’ IND (US and MHRA) and NDA filings; executed regulatory strategy/timeline and budget/resources in alignment with FDA/ICH guidance for API, product development and product stability. , Operations – built and maintained effective business/personal relationships in the US and other countries (UK, Italy, Spain, Australia, New Zealand), experienced as contract manufacturer and outsource customer.

These are some of the questions we asked our climbers about their experiences with Center For Pharmaceutical Science And Technology: