WHY YOU?

Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

• Graduate (or equivalent) qualification or equivalent time in role
• Attention to detail, ability to function in an atmosphere of constant change with detailed accuracy. Working knowledge of analytical techniques, manufacturing, packaging, and stability testing procedures.
• Demonstrate good leadership qualities and interpersonal skills.
• An in-depth knowledge of cGLP, cGMP’s and SOP’s throughout GMS and Quality Assurance.
• Detailed knowledge and understanding of Out of specification investigations and regulatory requirements.
• Understanding / ability to demonstrate use of continuous improvement techniques.

Please take a copy of the Job Description, as this will not be available post closure of the advert.
When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.

To lead and motivate a team of analysts to carry out analytical checks of products in a compliant and timely manner.
We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.
Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK

In this role you will:

• Responsible for testing, approval review of raw materials, intermediates and finished products ensuring accuracy, completeness, adherence to specifications
• Responsible for the management of out of specification investigations within the team and presenting OOS final review form to QP for sign off. Periodic review of trends and take ownership of corrective actions to improve laboratory not right first time levels.
• Responsible for a team of QC analysts providing guidance, support and training to ensure high performance in line with GSK people policies.
• Responsible for promoting and following site and laboratory safety practises to ensure compliance with EHS regulations
• Identify and implement opportunities within QC processes to enhance efficiency and reduce errors through the GSK Global Production System (GPS)