Quality Assurance Specialist

SRG; England; On-site; GBP 28,000 - 38,000; Full time

Job summary

SRG is recruiting a QA Officer for a well-established GMP manufacturing site in Norfolk. You will work within the QA team to uphold the highest quality standards across processes and products.

Key duties include controlling and reviewing quality documentation, supporting CAPA and QP batch release activities, and driving continuous improvement through quality projects. A scientific degree and GMP QA experience are required.

Qualifications

• Degree or equivalent in a relevant scientific/pharmaceutical field.
• Experience in QA within an GMP environment.
• Excellent attention to detail and passion for quality.
• Strong communication and liaison skills.

Responsibilities

• Control, prepare, review and approve quality documentation.
• Assist in GMP training program delivery.
• Investigate GMP breaches and OOO incidents.
• Support CAPA initiation and implementation.
• Support QP batch release activities.
• Contribute to continuous improvement and quality projects.

Skills

Attention to detail

Quality assurance

Communication

Education

Degree in science

Job description

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 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.