Responsibilities:

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Operate, set up and monitor semisolid production equipment to meet quality and production targets.
• Complete clear and accurate production and batch records according to procedures.
• Perform line clearances, cleaning, and shift handovers to keep the work area safe and compliant.
• Support preventive and unplanned maintenance and work with engineering to reduce downtime.
• Identify and raise issues, support investigations, and help implement corrective actions.
• Suggest and support continuous improvement ideas to increase efficiency and reduce waste.

Why you?

Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• High school diploma or equivalent; technical or vocational diploma is an advantage.
• Minimum 1 year relevant experience in manufacturing, processing or technical operations.
• Willingness to work on-site and follow shift patterns, including nights or weekends as required.
• Ability to follow written procedures and keep accurate records.
• Good attendance, punctuality and a strong safety mindset.
• Willingness to learn digital production systems such as SAP or other electronic record systems.

Preferred Qualification:

If you have the following characteristics, it would be a plus:

• 2 5 years experience in pharmaceutical, food or other regulated manufacturing environments.
• Technical diploma or associate degree in a relevant field.
• Basic English reading skills to follow procedures and read documentation.
• Experience with Good Manufacturing Practice (GMP) and data integrity principles.
• Experience in continuous improvement activities or use of improvement tools.
• Basic computer skills and experience with electronic batch records or ERP systems

How to apply?

If this role feels like the right step for you, we would love to hear from you. Please submit your CV and a short note explaining your interest and what you hope to achieve in this role. If you need support with your application or require reasonable adjustments, contact our recruitment team and we will support you. Applications are reviewed on a rolling basis apply soon.

Skills

• Data Integrity
• Detail-Oriented
• Digital Fluency
• Emergency Response
• Financial Acumen
• GxP Regulations
• Lean Management
• Manufacturing Processes
• Problem Solving
• Production Management
• Project Coordination
• Quality Compliance
• Regulatory Compliance
• Risk Awareness
• Site Operations

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Contact information:

You may apply for this position online by selecting the Apply now button.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Desired Candidate Profile

• High school diploma or equivalent; technical or vocational diploma is an advantage.
• Minimum 1 year relevant experience in manufacturing, processing or technical operations.
• Willingness to work on-site and follow shift patterns, including nights or weekends as required.
• Ability to follow written procedures and keep accurate records.
• Good attendance, punctuality and a strong safety mindset.
• Willingness to learn digital production systems such as SAP or other electronic record systems.
• 2 5 years experience in pharmaceutical, food or other regulated manufacturing environments.
• Technical diploma or associate degree in a relevant field.
• Basic English reading skills to follow procedures and read documentation.
• Experience with Good Manufacturing Practice (GMP) and data integrity principles.
• Experience in continuous improvement activities or use of improvement tools.
• Basic computer skills and experience with electronic batch records or ERP systems