Center For Pharmaceutical Science And Technology Work Values

Daily Duties at Center For Pharmaceutical Science And Technology:

Developed HPLC assays for small molecules and proteins. Generated reports summarizing formulation/analytical data. Directed regular interaction with clients and presented data to clients during meetings. Transformed problematic formulations leading to an increased shelf life for products.

What they like about Center For Pharmaceutical Science And Technology:

Working for a company with an emphasis on social values and helping society is a clear and important priority for you - a critical factor in who you choose to work for. In contrast to other factors, you place an organization's reputation for fairness and concern for the community above most other aspects of the company. As you search for a new job opportunity, it is usually possible to find out if the company is involved in the community and/or if it is addressing problems and issues in society. Pay special attention to non-profit organizations and those specifically involved in social action. Moreover, speaking with current and former employees should enlighten you to perceptions of the fairness of the company's leaders and the treatment of employees.

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: