An excellent opportunity has arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company.

G-Pharm is the leading company in its field of research and development of prescription medicines to meet patient needs in a wide range of therapeutic indications.

The Role
Test and report on stability protocol time-points according to the relevant test methods, SOPs and protocols, under the direction of the Stability Laboratory Manager and/or Head of Analytical R&D.

Key Responsibilities
• The job holder is responsible for maintaining cGxP and H&S knowledge applicable to the job
• Perform all duties in accordance with safe working practices and where applicable GMP
• Provide clear and accurate records of all work performed
• Notify the Laboratory Manager and/or the Head of Analytical R&D of any OOS results
• Enter data into the appropriate records
• Report promptly any problems occurring at any phase of a study to the Laboratory Manager and/or the Head of Analytical R&D
• Ensure all equipment is fully calibrated and serviced in accordance with company procedures
• Maintain all areas of the laboratory in a clean and tidy state
• Work independently but readily provide support, training or coaching to other team members
• Ensure Compliance Wire Core SOPS are read
• Ensure any other relevant SOPs and Test methods have been read
• Ensure training records are kept up to date
• Carry out any other duties as required by the management

Essential Skills
Knowledge/Experience:
• Scientific based degree and laboratory experience
• Extensive practical experience with HPLC
• Previous experience with Dissolution Testing
• Previous experience of QC or Stability Analysis
• Previous experience of working in a GMP environment

Skills:
• Competent in the use of general laboratory instrumentation and devices e.g. pipettes, balances etc.
• Working knowledge of Excel and Word
• Excellent attention to detail - the job role requires checking of analytical data, reviewing of SOP’s, Test Methods, Protocols and Reports
• Communication skills including written and verbal - the job role requires writing of various analytical documents including Test methods, SOPs and protocols

To apply please send your CV with salary expectations via the apply online button:

Due to the high volume of applications we receive if you do not hear from us within two weeks of applying then unfortunately you have not been successful on this occasion. We do thank you for your interest in working for G-Pharm and wish you every success with future applications