An excellent development opportunity for an experienced Quality Assurance professional to join one of our global pharma clients in the capacity of QA Manager. This role holds full accountability for the UK and Ireland and offers the opportunity to work on global projects alongside the Global QA Director. This is a highly visible role offering fantastic long-term growth and development opportunities.
Hospira is the world’s leading provider of injectable drugs and infusion technologies. Through its broad, integrated portfolio, Hospira is uniquely positioned to Advance Wellness™ by improving patient and caregiver safety while reducing healthcare costs. The company is headquartered in Lake Forest, Ill., and has approximately 14,000 employees. Learn more at www.hospira.com.
This is an excellent opportunity for a QA Manager looking for an exciting challenge in this growing global pharma organisation. The role will be accountable for QA activities relating to the manufacture, packaging, testing, storage and distribution of investigational medicinal products ensuring compliance with current GMP, internal Quality Systems, Corporate expectations and Industry Standards.
I am currently working with one of the World's leading Biopharmaceutical companies, based in Switzerland who are actively seeking a Senior GCP Professional to join their established and successful QA team. This role requires an experienced Auditing professional who is looking to join an expanding team. There is a real potential for future progression due to the companies excellent pipeline and plans over the coming years.
Salary: c £60-70,000 and 20% Bonus and Benefits
An excellent opportunity has arisen with a leading, global Pharmaceutical organisation for a highly experienced Quality Manager/QP to lead the quality activities for the Quality Assurance team, ensuring all goods manufactured and services provided by the organisation meet the quality requirements of the company, clients and regulatory authorities.
I am working with one of the most reputable and successful Biopharmaceutical companies Worldwide, who are actively seeking a Senior Clinical Quality Assurance Professional to join their expanding and growing organisation. The ideal candidate will be an experienced GCP Audit professional and will have conducted investigator site, vendor, system and other Audits. This opportunity is perfect for a Senior Auditor/Manager who is looking to join a company where they can truly build a career!
Quality Systems Manager, East Anglia / Cambridge Global Pharmaceutical Company
Quality Systems Manager required for a leading Pharmaceutical manufacturing site. You will be responsible for the implementation of quality improvement programs and will work closely with QA and plant management teams to assure systems are effectively implemented and maintained to ensure compliance with regulatory requirements. This is a permanent role and candidates must be eligible to work in the UK. ...
A fantastic opportunity has arisen for an experience Regulatory Affairs Manager to join a leading global pharmaceutical company in Belgium.
As the Regulatory Affairs Manager you will manage the Site Conformance team as well as provide site assistance. You will offer regulatory conformance and CMC expertise to ensure products issued from the site are in line with the receiving market and approved data.
I am currently recruiting for a contract Medical Writer on behalf of a specialist medical service provider. My client is looking for someone who has a strong understanding of CSRs as this will be a primary responsibility.
I am also recruiting for permanent medical writing opportunities, so if you are interested please forward your CV to the email address mentioned in the advert.
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her