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:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

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: