Quality Assurance Officer

SRG; Gorleston-on-Sea; On-site; GBP 32,000 - 42,000; Full time

Job summary

SRG is recruiting a Quality Assurance Officer to join a GMP manufacturing site in Norfolk. You will be part of the QA team, ensuring quality across processes and products while working with experienced QA professionals.

The role involves documenting control and approval of quality records, supporting CAPA processes, audits and batch release activities within a busy GMP setting. Strong attention to detail and excellent communication are essential.

Qualifications

• A degree or equivalent qualification/experience in a relevant scientific / Pharmaceutical field.
• Prior experience of Quality Assurance in a GMP Environment.
• Excellent attention to detail with a passion for Quality.
• Good communication skills with the ability to liaise & influence effectively.

Responsibilities

• Control, prepare, review and approve Quality documentation.
• Assist in the development and delivery of GMP quality training programs.
• Investigate GMP breaches and OOO incidents.
• Recommend, implement and review CAPAs.
• Support site audits and QP batch release activities.
• Contribute to ongoing continuous improvement and quality projects.

Skills

Quality Assurance

GMP Experience

Attention to detail

Communication skills

Education

Bachelor's degree in science

Job description

Quality Assurance Officer Norfolk

SRG are recruiting for a QA Officer to join a well established GMP manufacturing site based in Norfolk. The site manufactures a wide range of essential Pharmaceuticals, Medical devices and Personal care products.

Based within the QA team, you will be working alongside an experienced team of QA professionals to ensure the highest quality standards are maintained in a busy GMP manufacturing environment.

The Role

As a QA Officer, you will be responsible for ensuring & monitoring the quality of processes and products on site. Key duties will include:

• Controlling, Preparing, review & approval of Quality documentation.


• Assisting in the development & delivery of GMP quality related training programs.


• Investigating any GMP breaches OOO incidents


• Recommending, implementing & reviewing CAPAs


• Supporting site audits.


• Supporting QP batch release activities


• Supporting ongoing continuous improvement & quality projects.

Required

• A degree or equivalent qualification/experience in a relevant scientific / Pharmaceutical field.


• Prior experience of Quality Assurance in an GMP Environment.


• Excellent attention to detail with a passion for Quality


• Good communication skills with the ability to liaise & influence effectively.