Back to Job SearchOur client is seeking a talented Process Development Scientist to join a leading pharmaceutical company based in the Berkshire area. As the Process Development Scientist, you will play a pivotal role in the establishment of robust, fit-for-purpose injectable drug product manufacturing processes from toxicology studies or first in human until BLA approval.
This is an initial 12 month contract with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Process Development Scientist will be varied however the key duties and responsibilities are as follows:
1. As the Process Development Scientist, you will define and select drug product manufacturing processes and parameters for clinical manufacture, ensuring alignment with regulatory requirements.
2. As the Process Development Scientist, you will cooperate with a wide range of internal and external stakeholders, including contract manufacturing organizations, as part of a project team.
3. As the Process Development Scientist, you will design and execute lab studies related to drug product development activities, capture and analyse data, and author related documentation.
4. As the Process Development Scientist, you will provide support to ensure timely manufacture of stability and clinical drug product batches, including process performance qualification/validation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Process Development Scientist we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in liquid drug product development and/or manufacturing within the pharmaceutical industry.
3. A working knowledge and practical experience with cGMP manufacturing under aseptic conditions, such as vial, cartridge, and pre-filled syringe filling.
Key Words: Drug Product Manufacturing / Injectable Drug Products / Pharmaceutical Manufacturing / cGMP / Aseptic Processing / Drug Product Development / Stability Batches / Clinical Manufacture / Process Validation / Regulatory Submissions
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
This is an initial 12 month contract with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Process Development Scientist will be varied however the key duties and responsibilities are as follows:
1. As the Process Development Scientist, you will define and select drug product manufacturing processes and parameters for clinical manufacture, ensuring alignment with regulatory requirements.
2. As the Process Development Scientist, you will cooperate with a wide range of internal and external stakeholders, including contract manufacturing organizations, as part of a project team.
3. As the Process Development Scientist, you will design and execute lab studies related to drug product development activities, capture and analyse data, and author related documentation.
4. As the Process Development Scientist, you will provide support to ensure timely manufacture of stability and clinical drug product batches, including process performance qualification/validation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Process Development Scientist we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in liquid drug product development and/or manufacturing within the pharmaceutical industry.
3. A working knowledge and practical experience with cGMP manufacturing under aseptic conditions, such as vial, cartridge, and pre-filled syringe filling.
Key Words: Drug Product Manufacturing / Injectable Drug Products / Pharmaceutical Manufacturing / cGMP / Aseptic Processing / Drug Product Development / Stability Batches / Clinical Manufacture / Process Validation / Regulatory Submissions
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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