Tecnico de Produccion (Temporal)

634 Glaxo Wellcome, S.A.; Aragón; On-site; EUR 38,000 - 64,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive program

Job summary

GlaxoSmithKline plc is seeking an on-site specialist to support the production of oral solid dosage products in Spain. You will collaborate with operators, engineers and quality teams to keep lines safe, compliant, and efficient.

We value hands-on problem solvers who learn quickly and can lead small improvement projects within a GMP environment, contributing to patient outcomes.

Qualifications

• University degree or vocational qualification in engineering, pharmacy, chemistry or a related technical field, or equivalent practical experience.
• At least 2 years’ experience in a pharmaceutical or regulated manufacturing environment.
• Practical knowledge of GMP and quality practices in pharmaceutical industry.
• Experience working on oral solid dosage packaging lines.
• Basic user skills in production systems such as SAP or electronic batch records.

Responsibilities

• Operate and monitor OSD packaging lines (Blister and Bottle) to meet production plans, safety and quality targets.
• Investigate deviations, support root cause analysis, and help implement corrective and preventive actions.
• Follow, maintain and suggest improvements to Standard Operating Procedures and work instructions.
• Support internal and external audits and help maintain compliance with Good Manufacturing Practice (GMP).
• Record production data accurately and use SAP or local systems for transactions and reporting.
• Contribute to continuous improvement projects using practical problem solving and production data.

Skills

GMP knowledge

Deviation investigation

CAPA

Lean Six Sigma

Automation awareness

Problem solving

Regulatory compliance

Data integrity

FDA/regulatory experience

Education

University degree in engineering, pharmacy, chemistry or related technical field

Tools

SAP

Electronic batch records

Job description

Business Introduction

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccine manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary

You will support on-site production of oral solid dosage (OSD) products. You will work with operators, engineers and quality colleagues to keep production lines safe, compliant and efficient. We value hands‑on problem solvers who learn quickly and share ideas. This role offers clear growth opportunities to build technical skills, lead small improvement projects and contribute to work that helps patients. Join us to unite science, technology and talent to get ahead of disease together.

Responsibilities

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

• Operate and monitor OSD packaging lines (Blister and Bottle) to meet production plans, safety and quality targets.
• Investigate deviations, support root cause analysis, and help implement corrective and preventive actions.
• Follow, maintain and suggest improvements to Standard Operating Procedures and work instructions.
• Support internal and external audits and help maintain compliance with Good Manufacturing Practice (GMP).
• Record production data accurately and use SAP or local systems for transactions and reporting.
• Contribute to continuous improvement projects using practical problem solving and production data.

Why You?

Basic Qualifications

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

Basic Qualifications

• University degree or vocational qualification in engineering, pharmacy, chemistry or a related technical field, or equivalent practical experience.
• At least 2 years’ experience in a pharmaceutical or regulated manufacturing environment.
• Practical knowledge of GMP and quality practices in pharmaceutical industry.
• Experience working on oral solid dosage packaging lines.
• Basic user skills in production systems such as SAP or electronic batch records.

Preferred Qualifications

• Experience with continuous improvement methods such as Lean or Six Sigma.
• Experience in deviation investigation, CAPA and structured root cause analysis.
• Familiarity with automation, process control systems, or industrial digital tools.
• Experience in problem-solving or improvement methodologies (for example Orange Belt/Green Belt).
• Experience in FDA-regulated environments or working with international supply chains.

Location and Working Model

This is an on-site position in Spain. You will be based at the manufacturing site and work closely with production and engineering teams.

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 Spanish

Salary Range / Rango salarial en España

EUR 38,100 to EUR 63,500. The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.

Why GSK?

We are a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Find out more on our career site.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.