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Latest HRS Jobs
QA Officer

J5342WiltshirePharmaceutical
Permanent£25,000 to £30,000 per annumFull Time11/04/2018Quality Assurance
Quality Assurance – Auditing
Quality Assurance – Compliance
Quality Assurance - Validation
Quality Assurance – GMP
Quality Assurance – GLP
Quality Assurance - GDP
Quality Assurance – GCP
Quality Assurance - ISO9001
Quality Assurance - GxP
Permanent£25,000 to £30,000 per annumFull Time11/04/2018Quality Assurance
Quality Assurance – Auditing
Quality Assurance – Compliance
Quality Assurance - Validation
Quality Assurance – GMP
Quality Assurance – GLP
Quality Assurance - GDP
Quality Assurance – GCP
Quality Assurance - ISO9001
Quality Assurance - GxP
Further Information
Job Description:
Hyper Recruitment Solutions are currently looking for a Quality Assurance Officer to join a leading Pharmaceutical company based in the Wiltshire area. As the Quality Assurance Officer you will be responsible for maintaining GMP compliance across the manufacturing site.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:
1. You will be maintaining high quality processes, ensuring compliance to GMP and MHRA and FDA regulations through product development from the development phase (equipment and process validation), through to commercialisation, working with a wide variety of products.
2.You will be responsible for making sure staff are adhering to SOP's throughout business areas including manufacturing, packaging and cleanroom environments.
3. You will be responsible for completing internal area and system audits, whilst taking appropriate action to ensure full compliance with SOP's, working in a fast-paced environment.
4. Completing reviews and closures of batch records with associates. You will gain experience of validating equipment involved in the sterile manufacture of a pharmaceutical product.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Quality Assurance Officer we are looking to identify the following on your profile and past history:
1. Relevant degree in a science based discipline, (Biology, Chemistry, Pharmacy).
2. Proven industry experience in a pharmaceutical Quality Assurance setting, working within a QMS system.
3. A working knowledge and practical experience with the production of a sterile pharmaceutical product, and manufacture of products as set out in the Orange Guide.
Key Words: | GMP | cGMP | Quality Assurance | QA | Sterile | Licensed Medicines | Quality Management System | Change Control | CAPA's | Deviations | Supplier Management | Compliance | Audits | Specialist | Associate | Aseptic | Biologics | Quality | Clean Rooms | LIMS | IQ | OQ | PQ |
Hyper 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.
Hyper Recruitment Solutions are currently looking for a Quality Assurance Officer to join a leading Pharmaceutical company based in the Wiltshire area. As the Quality Assurance Officer you will be responsible for maintaining GMP compliance across the manufacturing site.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:
1. You will be maintaining high quality processes, ensuring compliance to GMP and MHRA and FDA regulations through product development from the development phase (equipment and process validation), through to commercialisation, working with a wide variety of products.
2.You will be responsible for making sure staff are adhering to SOP's throughout business areas including manufacturing, packaging and cleanroom environments.
3. You will be responsible for completing internal area and system audits, whilst taking appropriate action to ensure full compliance with SOP's, working in a fast-paced environment.
4. Completing reviews and closures of batch records with associates. You will gain experience of validating equipment involved in the sterile manufacture of a pharmaceutical product.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Quality Assurance Officer we are looking to identify the following on your profile and past history:
1. Relevant degree in a science based discipline, (Biology, Chemistry, Pharmacy).
2. Proven industry experience in a pharmaceutical Quality Assurance setting, working within a QMS system.
3. A working knowledge and practical experience with the production of a sterile pharmaceutical product, and manufacture of products as set out in the Orange Guide.
Key Words: | GMP | cGMP | Quality Assurance | QA | Sterile | Licensed Medicines | Quality Management System | Change Control | CAPA's | Deviations | Supplier Management | Compliance | Audits | Specialist | Associate | Aseptic | Biologics | Quality | Clean Rooms | LIMS | IQ | OQ | PQ |
Hyper 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.
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