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Laboratory Support Supervisor

GloucestershirePermanent
Experience Dependant
Job Reference: J5632046
Updated On: 10/09/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Manufacturing Organisation

Skills: Chemistry - Analytical - Team Leader / Supervisor (5 staff max), Chemistry - Analytical - Development and Validation Analyst, Validation - Equipment Validation, Validation - Cleaning Validation

Job Information

Role Overview

We are currently looking for a Laboratory Support Supervisor to join a leading Heath Care company based in the Gloucestershire area. As the Laboratory Support Supervisor you will be responsible for overseeing the stability program, performing validation testing, cleaning validation studies, method transfers and analytical method development. As well as equipment procurement, qualification, validation and completing IQ OQ PQ documentation.

Key Duties and Responsibilities

Your duties as the Laboratory Support Supervisor will be varied however the key duties and responsibilities are as follows:

1. As the Laboratory Support Supervisor you will Liaise and supervisor laboratory contract service providers. Oversee the Analytical method Development and Validation, schedule and produce annual report for the Validation Master Plan.

2. You will perform analytical work for method transfers and carry out training of Quality Control staff where necessary and associated reporting as well as taking as a supervisory role establishing and maintaining Laboratory Support KPIs.

3. As the Laboratory Support Supervisor you will have an understanding of the process of equipment procurement and lead IQ/OQ/PQ projects for the lab.

4. You will ensure the design and implementation of qualification/validation studies for equipment/systems/processes and subsequent reporting. As well as ensure laboratory equipment is suitably qualified, calibrated and maintained.

Role Requirements

To be successful in your application to this exciting opportunity as the Laboratory Support Supervisor we are looking to identify the following on your profile and past history:

1. Relevant degree in a scientific discipline or equivalent industry experience.

2. Proven industry experience in Analytical method development and validation within a healthcare or pharmaceutical company.

3. A working knowledge and practical experience with equipment qualification, validation, calibration and maintenance.


Key Words: IQ, OQ, PQ, Cleaning Validation, Equipment Validation, Validation Master Plan, Equipment Qualification, Method Development, Method Validation.
Edward McNulty
Your Recruitment ConsultantEdward McNultyEdward.mcnulty@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We 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 recruitment processionals and scientists. We look forward to helping you with your next career moves.