Records Management - Physicochemistry

RECORDS MANAGEMENT, PHYSICOCHEMISTRY

Apply now for the position to work as a Consultant for Analytical Methods Validation in the Physicochemistry group from QC. You will be working for a highly reputable multinational CRO. If you are looking to boost your profile with a key player in the market then this is the opportunity for you.

KEY RESPONSIBILITIES

Manage and organize analytical methods and Physical reagents validation activities

for the entire QC Physicochemistry group:

Estimation of workload and planification of activities for the entire Biochemistry group

Follow-up of established planning

Reporting to Physicochemistry management

Produce analytical methods and biological reagents validation files:

Establish strategy for methods to validate and reagents to bridge in collaboration with

supervisor in charge of the method

Translate strategy into validation protocol and experimental plan and communicate with

supervisor and lab technicians in charge of the method

Follow-up of experiments related to validations with laboratories and collect data

Redaction of validation reports and submission to Validation Manager and QA

Expert review of validation data & documents (protocols/reports).

SKILLS REQUIRED:

- Scientific degree
- Bilingual French/English, written competencies in English
- Experience in pharma & GMP is an asset.
- Experience in analytical techniques is an asset and knowledge of biochemical technique
- (ELISA, MSD-HPLC, gel electrophoresis) is highly recommended.
- Confirmed experience in analytical method & reagents validation is highly recommended

Please contact Michael Bailey Associates and ask for Hardeep Dhillon. Michael Bailey International is acting as an Employment Business in relation to this vacancy.