Process Technologist - 12 Month FTC/Secondment - Multiple Positions Available

GlaxoSmithKline plc; Eggleston; On-site; GBP 35,000 - 52,000; Full time

Benefits offered by this job

Annual bonus

Healthcare

Pension plan

Shares scheme

Job summary

GlaxoSmithKline plc in the United Kingdom is seeking a Process Technologist to join a team supporting the production area, delivering technical service, new product introductions and troubleshooting in a GMP/EHS-compliant environment.

You will design and optimise manufacturing processes, validate new technologies through tech transfer with R&D, and manage multiple projects with a data-driven approach to maintain high quality and productivity.

Qualifications

• Bachelors/Masters/PhD degree in Chemistry, Biology, Engineering or another related field.
• Technical or industry experience within pharmaceuticals or biotechnologies.
• Excellent problem-solving and analytical skills.
• Effective communication and teamwork abilities.
• Experience with cGMP, industry standards and regulatory requirements.

Responsibilities

• Process Design, Development and Improvement: Design and develop manufacturing processes to improve efficiency and quality while reducing waste.
• Process Validation: Input into specifications and assist tech transfer and validation of processes.
• Project Delivery: Manage multiple priorities and deliver project milestones in an agile way.
• Operational Support: Diagnose and resolve process issues using RCA and monitor performance with data.
• Quality Compliance: Lead or assist in FMEAs, risk assessments, deviations, change controls and CAPA closures.
• Safety Compliance: Ensure processes adhere to safety regulations and policies.

Skills

Problem solving

Analytical skills

Communication

Teamwork

Education

Bachelor's/Master's/PhD in Chemistry, Biology, Engineering

Job description

As a Process Technologist, you will work as part of a team supporting the production area providing a technical service. This will involve provision of a New Production Introduction, troubleshooting, working on technical projects & supply of technical data. Your role will span work undertaken in the production environment. All work must be conducted in compliance with specified GMP and EHS standards.,

• Process Design, Development and Improvement: Design and develop manufacturing processes for new products and optimise existing processes to improve efficiency and quality in line with regulatory requirements. Identify and implement process improvements using lean manufacturing, Six Sigma, and other methodologies to increase productivity and reduce waste.
• Process Validation: Input into the specification for new process technologies to enhance production capabilities. Work with R&D and global functions for the tech transfer and validation of processes.
• Project Delivery: Be able to manage a number of priorities and work in an agile way to deliver project milestones.
• Operational Support: Diagnose and resolve process-related issues using root cause analysis (RCA) techniques to minimise downtime and ensuring smooth production operations. Collect and analyse process data to monitor performance, identify trends, and drive data-driven decision-making.
• Quality Compliance: Lead or assist in FMEAs, risk assessments, deviations, change controls, and corrective and preventive action closures.
• Safety Compliance: Ensure all manufacturing processes adhere to safety regulations and company policies to maintain a safe working environment. Bachelors/Masters/PHD degree in Chemistry, Biology, Engineering or another related field.
• Technical or industry experience within pharmaceuticals or biotechnologies.
• Excellent problem-solving and analytical skills.
• Effective communication and teamwork abilities.
• Experience with cGMP, industry standards and regulatory requirements.

Preferred Qualifications & Skills:

• Strong knowledge of lean manufacturing, Six Sigma, and other process improvement methodologies.
• Strong project management and self-organisation skills., CMC Strategy, Data-Driven Decision Making, Data Integrity, Debate Moderation, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Process Optimization, Project Leadership, Risk Awareness, Scientific Writing, Technology Transfer

GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases, and as a key supplier of some of GSK's blockbuster products, the site contributes revenues of ~$2Bn annually., 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. 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. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at [e-mail] where you can also request a call. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. 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. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov

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