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Our client is seeking a skilled Validation Specialist to join a leading pharmaceutical company based in the LOCATION area. As the Validation Specialist, you will play a crucial role in addressing a significant deviation within a biological bulk production facility. This assignment is initially planned for 3 months, with a preferred start date before August 4th.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Specialist will be varied; however, the key duties and responsibilities are as follows:
1. Actively participate in the investigation within a multidisciplinary team.
2. Coordinate qualification and validation activities related to the deviation.
3. Draft impact analysis and qualification/validation documentation in compliance with GMP.
4. Execute and/or review qualification tests, such as HVAC and thermal validation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Validation Specialist, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Extensive industry experience in pharmaceutical validation.
3. A working knowledge and practical experience with GMP, CFR, and pharmaceutical manufacturing processes.
4. Fluent in French
Key Words:
Validation Specialist / Pharmaceutical Validation / GMP / CFR / Qualification / Validation / HVAC / Thermal Validation / Cleaning Validation / Sterilization / Pharmaceutical Manufacturing
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 is seeking a skilled Validation Specialist to join a leading pharmaceutical company based in the LOCATION area. As the Validation Specialist, you will play a crucial role in addressing a significant deviation within a biological bulk production facility. This assignment is initially planned for 3 months, with a preferred start date before August 4th.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Specialist will be varied; however, the key duties and responsibilities are as follows:
1. Actively participate in the investigation within a multidisciplinary team.
2. Coordinate qualification and validation activities related to the deviation.
3. Draft impact analysis and qualification/validation documentation in compliance with GMP.
4. Execute and/or review qualification tests, such as HVAC and thermal validation.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Validation Specialist, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Extensive industry experience in pharmaceutical validation.
3. A working knowledge and practical experience with GMP, CFR, and pharmaceutical manufacturing processes.
4. Fluent in French
Key Words:
Validation Specialist / Pharmaceutical Validation / GMP / CFR / Qualification / Validation / HVAC / Thermal Validation / Cleaning Validation / Sterilization / Pharmaceutical Manufacturing
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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