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Our client, a leading company in the Biopharmaceutical industry is seeking a Technical Expert to join their team on a 12-month contract based in the Berkshire area. This role offers an exciting chance to contribute to the establishment of robust, fit-for-purpose injectable drug product manufacturing processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Technical Expert will be varied; however, the key duties and responsibilities are as follows:
1. Define and select drug product manufacturing processes and parameters for clinical manufacture.
2. Design and execute lab studies related to drug product development activities, capturing and analysing data.
3. Cooperate with a wide range of internal and external stakeholders, including contract manufacturing organisations, as part of a project team.
4. Provide support to ensure timely manufacture of stability and clinical drug product batches.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Technical Expert, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific 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.
Key Words:
Pharmaceutical Development / Drug Product Manufacturing / Injectable Drug Products / Clinical Manufacture / cGMP / Aseptic Conditions / Process Development / Liquid Drug Products / Stability Batches / Regulatory Submissions / CMC / sterile / liquid / GMP
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.
Our client, a leading company in the Biopharmaceutical industry is seeking a Technical Expert to join their team on a 12-month contract based in the Berkshire area. This role offers an exciting chance to contribute to the establishment of robust, fit-for-purpose injectable drug product manufacturing processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Technical Expert will be varied; however, the key duties and responsibilities are as follows:
1. Define and select drug product manufacturing processes and parameters for clinical manufacture.
2. Design and execute lab studies related to drug product development activities, capturing and analysing data.
3. Cooperate with a wide range of internal and external stakeholders, including contract manufacturing organisations, as part of a project team.
4. Provide support to ensure timely manufacture of stability and clinical drug product batches.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Technical Expert, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific 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.
Key Words:
Pharmaceutical Development / Drug Product Manufacturing / Injectable Drug Products / Clinical Manufacture / cGMP / Aseptic Conditions / Process Development / Liquid Drug Products / Stability Batches / Regulatory Submissions / CMC / sterile / liquid / GMP
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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