Back to Job SearchROLE OVERVIEW
A leading pharmaceutical company based in the Walloon region of Belgium is seeking a dedicated Production Supervisor to join their dynamic team. As the Production Supervisor, you will play a pivotal role in leading a team of technicians and operators, ensuring the safety, quality, and efficiency of the closed system (liquid) production processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Production Supervisor will be varied however the key duties and responsibilities are as follows:
1. Apply and enforce safety requirements and GMP rules, ensuring compliance with SOPs and regulations.
2. Organise departmental activities, including document and batch record revisions, and coordinate with stakeholders such as Planning, QC, and QA.
3. Lead and develop CAPA initiatives to enhance processes and support new projects, fostering innovation.
4. Participate in production activities to maintain a strong connection with the floor and provide assistance to meet production objectives.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Production Supervisor we are looking to identify the following on your profile and past history:
1. Relevant degree in a related field.
2. Proven industry experience in a pharmaceutical or GMP-regulated environment.
3. A working knowledge and practical experience with traditional software and GMP/ISO regulations.
Key Words:
Production Supervisor / Pharmaceutical / GMP / ISO 9001 / ISO 13485 / 21CFR820 / Quality Assurance / CAPA / Walloon / Belgium / Team Leadership / Process Improvement / Safety Compliance
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.
A leading pharmaceutical company based in the Walloon region of Belgium is seeking a dedicated Production Supervisor to join their dynamic team. As the Production Supervisor, you will play a pivotal role in leading a team of technicians and operators, ensuring the safety, quality, and efficiency of the closed system (liquid) production processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Production Supervisor will be varied however the key duties and responsibilities are as follows:
1. Apply and enforce safety requirements and GMP rules, ensuring compliance with SOPs and regulations.
2. Organise departmental activities, including document and batch record revisions, and coordinate with stakeholders such as Planning, QC, and QA.
3. Lead and develop CAPA initiatives to enhance processes and support new projects, fostering innovation.
4. Participate in production activities to maintain a strong connection with the floor and provide assistance to meet production objectives.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Production Supervisor we are looking to identify the following on your profile and past history:
1. Relevant degree in a related field.
2. Proven industry experience in a pharmaceutical or GMP-regulated environment.
3. A working knowledge and practical experience with traditional software and GMP/ISO regulations.
Key Words:
Production Supervisor / Pharmaceutical / GMP / ISO 9001 / ISO 13485 / 21CFR820 / Quality Assurance / CAPA / Walloon / Belgium / Team Leadership / Process Improvement / Safety Compliance
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.
Your Recruitment Consultant
Share this Job
