QA/RA Pharmaceutical Senior Specialist

Real Staffing
11 Sep 2018
17 Sep 2018
Contract Type
Full Time
Essential Functions:

Extensive knowledge in cGMP / Pharma regulations, with a minimum of 10 years proven experience in a relevant field.
Previous experience of submitting, and maintaining a site for a drug license (Phase II clinical use only)
Previous experience in document design
Good project Management skills, with the expectation of managing the project, and liaising with the customer of key milestones / deliverables
Perform certain Customer Support activities with existing customers as directed.


10+ years of Regulatory experience, preferably in pharma drug development.
Bachelors degree in relevant field.
Exceptional organizational, communication (verbal and written) and interpersonal skills.
Business acumen and Customer Relationship Management skills.
Effective PC skills including Excel, Word, PowerPoint and Outlook.
Ability to work independently and remotely. Position allows flexible schedule and is not expected to require F/T hours. Visits to the UK office (Glasgow, would be expected 12 days per month, minimum)

To find out more about Real please visit

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy Registered office 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom Partnership Number OC387148 England and Wales Advertised through Zoek 868c86eba54e4929be5302c31d5d2ee59

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