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:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

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: