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Process Development Associate

KentPermanent
£37,000 - £46,000 per annum
Job Reference: J5634842
Updated On: 18/05/2021
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Biotechnology

Skills: Biochemistry - Fermentation / USP, Biochemistry - Manufacturing / Plant Scale Purification, Quality Assurance - GMP, Biochemistry - Technology Transfer, Process Development - Biotechnology / Biopharma

Job Information

Role Overview

We are currently looking for a Process Development Associate to join a leading Biopharmaceutical company based in the Kent area. As the Process Development Associate you will be responsible for qualifying and introducing new fermentation biotechnology processes for the transition into production.

Key Duties and Responsibilities

Your duties as the Process Development Associate will be varied however the key duties and responsibilities are as follows:

1. You will work closely with internal research staff, contributing to the design of experiments, qualifying the performance of equipment and ensuring projects are in accordance with any quality, regulatory and collaborator requirements.

2. You will author and approve a range of documentation including Technology Transfer, Process Qualification and Process Outline documentation.

3. As the Process Development Associate, you will identify opportunities to improve manufacturing processes and initiate Process Change documentation.

4. You will support the completion of new collaborator projects, working closely with R&D staff to support the process development and project execution.

Role Requirements

To be successful in your application to this exciting opportunity as the Process Development Associate we are looking to identify the following on your profile and past history:

1. Relevant BSc, MSc or PhD in a scientific discipline e.g. Biochemical Engineering, Biotechnology, Bioprocessing

2. Proven industry experience in a Process Development or Technology Transfer role working closely with fermentation biopharmaceutical processes.

3. A working knowledge and practical experience with process driven documentation or production regulations e.g. GMP regulations, ISO regulations, Process Qualification documentation

Key Words: Process Development | Fermentation | Technology Transfer | Tech Transfer | Bioprocessing | Bioprocess | Biopharmaceutical | Biochemical Engineering | GMP | ISO | Process Qualification | Process Outline | Process Change | Quality System | Kent | South East | CDMO |
Jogesh Bowry
Your Recruitment ConsultantJogesh Bowryjogesh.bowry@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.