Explore recent issues of Contract Pharma covering key industry trends.
Read the full digital version of our magazine online.
Stay informed! Subscribe to Contract Pharma for industry news and analysis.
Get the latest updates and breaking news from the pharmaceutical and biopharmaceutical industry.
Discover the newest partnerships and collaborations within the pharma sector.
Keep track of key executive moves and promotions in the pharma and biopharma industry.
Updates on the latest clinical trials and regulatory filings.
Stay informed with the latest financial reports and updates in the pharma industry.
Expert Q&A sessions addressing crucial topics in the pharmaceutical and biopharmaceutical world.
In-depth articles and features covering critical industry developments.
Access exclusive industry insights, interviews, and in-depth analysis.
Insights and analysis from industry experts on current pharma issues.
A detailed look at the leading US players in the global pharmaceutical and BioPharmaceutical industry.
Browse companies involved in pharmaceutical manufacturing and services.
Comprehensive company profiles featuring overviews, key statistics, services, and contact details.
A comprehensive glossary of terms used in the pharmaceutical and biopharmaceutical industry.
Watch in-depth videos featuring industry insights and developments.
Listen to expert discussions and interviews in pharma and biopharma.
Download in-depth eBooks covering various aspects of the pharma industry.
Access detailed whitepapers offering analysis on industry topics.
View and download brochures from companies in the pharmaceutical sector.
Explore content sponsored by industry leaders, providing valuable insights.
Stay updated with the latest press releases from pharma and biopharma companies.
Explore top companies showcasing innovative pharma solutions.
Meet the leaders driving innovation and collaboration.
Engage with sessions and panels on pharma’s key trends.
Hear from experts shaping the pharmaceutical industry.
Join online webinars discussing critical industry topics and trends.
A comprehensive calendar of key industry events around the globe.
Live coverage and updates from major pharma and biopharma shows.
Find advertising opportunities to reach your target audience with Contract Pharma.
Review the editorial standards and guidelines for content published on our site.
Understand how Contract Pharma handles your personal data.
View the terms and conditions for using the Contract Pharma website.
What are you searching for?
Dick will be responsible for all manufacturing operations
November 25, 2013
By: Tim Wright
Editor-in-Chief, Contract Pharma
Catherine Dick has been appointed to the new role of site manufacturing manager at Aesica’s Cramlington, UK facility. Ms. Dick will be responsible for all manufacturing operations from product introduction through all aspects of the manufacturing process. She will also work to ensure that activities are kept on schedule for products during the remainder of 2013, including the completion of manufacturing on approximately four new products due to be brought on to the Cramlington site in 2014. Ms. Dick brings extensive experience and knowledge of operations at Cramlington, having joined Aesica in 2007 as the site’s quality manager. In 2010, she was promoted to head of Quality for UK API, responsible for the quality and regulatory compliance of all products manufactured across both the Cramlington and the Queenborough API manufacturing sites. Recently, she headed the latest Queenborough API MHRA site inspection. Also, Mark Dawson has been appointed head of Quality at the Cramlington facility. He has more than 25 years of experience in the API industry having held various roles at the site within the Quality Control, EH&S and Warehousing departments. In his most recent role, he spent 13 years as part of the production management team responsible for the day-to-day running of the process plants at the Cramlington site. Steve Barker, operations director, API Business Unit at Aesica said, “Catherine possesses strong expertise and a solid knowledge of implementing work on multiple, quality APIs. The acumen she brings to the role coupled with the collective quality measures we are taking will ensure the company operates to the most rigorous, cost effective and timely manufacturing processes.”
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !