Product Technologist

Are you looking to enhance your technical capability by working in a global manufacturing environment that allows you to leverage state-of-the-art systems and technologies?  If so, this Product technologist role in Manufacturing science and technology functions could be an ideal opportunity to explore.

 

As an MSAT (Manufacturing Science & Technology) Technologist, you operate within a cross-functional environment to deliver technical expertise and support continuous improvement initiatives. Your responsibilities include conducting technical assessments related to materials, evaluating and optimizing manufacturing processes, and ensuring robust validation strategies.

You play a key role in driving development and improvement projects within operations by:

• Assessing and troubleshooting material-related issues
• Identifying and implementing process optimization opportunities
• Supporting process validation and lifecycle management activities
• Collaborating with Quality, Production, Engineering, and R&D teams
• Ensuring compliance with regulatory and quality standards

 

Responsibilities:

• Assist in maintaining Product Quality Lifecycle documentation including Product Control Strategy, Technical Risk Assessments, and Continued Process Verification.
• Assist in developing product strategies and technical risk assessment for early-stage PLM activities.
• Participate in change control assessments (AL1/2) and contribute to impact analysis on product quality.
• Collaborate with cross-functional teams (Operations, Quality, Engineering) to support product-related investigations and improvements.
• Involve in packaging and manufacturing design enhancement and technologies to improvise the existing packaging and manufacturing processes.
• Provide input on improving PLM workflows and contribute to the implementation of best practices to enhance efficiency.
• Explore digital technologies to robust and simplify the process of technical risk assessments.
• Support management monitoring activities, internal audits, and inspections to ensure timely documentation and closure of CAPAs.
• Maintain awareness of regulatory and compliance requirements relevant to product lifecycle. Contribute to continuous improvement initiatives through data collection and technical evaluation.
• Support in execution of Process and Cleaning validation right from drafting protocol till Batch releases to the market.

 

Education, Experience and Skills

• Pharm -D, Chemist and Bio-chemistry is required for this role.
• 1-2 years or more of experience in R&D, Quality Control or Production operations
• Experience working in a Good Manufacturing Practices (GMP) environment
• Experience with Data Analytic skills with critical thinking
• Good understanding of compliance (Validations Cleaning and Process , Quality, Safety)
• Good written and verbal communications skills
• Solid computer skills (Excel, Word, Powerpoint)

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.