Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Freelance/Contract Qualified person (QP) - Small Biotech

Company: TEC Group International
Location:
Reference: MGGOSMQP
Closing Date: 28 Feb 19
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

Freelance QP / Contract QP / Qualified Person (QP) / Responsible Person (RP) / Authorized Person (AP)

Requirements:

Freelance QP / Contract QP / Qualified Person (QP) / Responsible Person (RP) / Authorized Person (AP)

I am currently working with an Innovative Biotech that continuously challenges itself to heighten its standards and accomplishments. They Pride themselves on having an excellent culture built with the sharpest minds in Biotech, resulting in a close community where you can see the tangible results of your contributions. Every individual matters to my client, with everyone having a chance to enhance their skills through ongoing development. This company allows you to get stuck into multiple areas with a variety of work to expand your experience.

 

Qualifications/Experience

  • Licence in pharmacy, biology or chemistry
  • Life Science degree
  • Experienced with final certification/release within the EU
  • Quality systems management, audit experience (internal and external) and a strong EU regulatory understanding
  • Experience in GMP Quality environment in a Quality assurance function
  • Experience in undertaking the routine duties of a Qualified Person as well as experience in auditing suppliers, API facilities, drug product manufacturing or testing sites and exposure to more than one dosage form

 

Responsibilities (include but not limited to)

  • Certifies that batches of medicinal products have been manufactured or assembled and checked in compliance with Member State law and in accordance with their Marketing Authorization
  • Certifies batches prior to use in a clinical trial
  • Certifies batches prior to release for sale and placing on the market
  • Ensures the supply chain is secure and counterfeit materials cannot be introduced in the system
  • Support the QA Director to maintain audit schedule
  • To ensure GMP compliance across the Pharmaceutical Services Organisation

 

My name is Megan, I am a consultant specialising within Quality Assurance, to find out about this opportunity, similar opportunities or get expert advice regarding your next step contact me via:

Phone: +44 2085443429

Email: mgoodwin@tgilifesciences.com

LinkedIn: linkedin.com/in/megan-g-821459103

Apply for this job: Freelance/Contract Qualified person (QP) - Small Biotech

Contact Information:

Address:  Head Office
Dowgate Hill House, 14-16 Dowgate Hill, London
EC4R 2SU
England
Tel:  +44 (0) 208 544 3400
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

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 physician.