Study Director / Project Manager

Location
Surrey
Salary
Experience dependant
Posted
15 Mar 2017
Closes
12 Apr 2017
Ref
J3601
Contact
Megan Rich
Contract Type
Permanent
Hours
Full Time
We are currently looking for a Study Director / Project Manager to join a growing pharmaceutical company based in the Surrey area. As the Study Director / Project Manager you will be responsible for leadership and flawless execution of method development scientific research studies in the required timeframe to a high quality standard in line with GxP and GMP regulations.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Study Director / Project Manager will be varied however the key duties and responsibilities are as follows:

1. Leading GMP Method Development studies acting as the single point of control through study lifecycle, ensuring work is scheduled and performed as per agreed study protocol for both GMP and GxP studies.

2. Write and review Method Development study protocols, reports, SOPs and policies to agreed timelines as defined by Project timelines. You will be required to manage several work stages simultaneously.

3. Technical Review / Scientific interpretation of data, highlighting any unusual or atypical results and leading appropriate investigations. You will be responsible for leading deviations, investigations, OOS or OOT investigations with minimal support.

4. You will liaise with customers about specific study results as required in support of analytical product representative and support customer audits and regulation.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Study Director / Project Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in a life sciences related discipline, plus relevant experience gained within a GMP BioPharmaceutical environment.

2. Proven industry experience with a range of analytical techniques, specifically chromatographic techniques such as HPLC and GC.

3. As this is a Senior role with client facing responsibilities, you will be expected to demonstrate excellent communication and organisational skills. You will also be expected to have experience working within the limits of safety, quality, cost and regulation.

Key Words: Project Manager | Study Director | Stability | Pharmaceutical | GMP | Analytical | Projects | HPLC | GC | Method Development | GxP | Chemistry

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors and is made up of a collaboration of scientists supporting science. We look forward to helping you with your next career moves.