Job Purpose
To support the technical lifecycle of pharmaceutical products at the site level by assisting in process monitoring, documentation, validation activities (Process and Cleaning Validation), and continuous improvement initiatives. The role contributes to maintaining product quality and compliance through hands-on technical support and collaboration across functions.
Education, Experience & Skills
Pharm-D, B.E, M.Sc Scientific, Technical, Industrial Pharmacy
1–2 years in pharmaceutical manufacturing or technical support roles
To ensure familiarity with GMP, validation practices, and product lifecycle support.
Strong organizational and time-management skills.
Effective communication and collaboration abilities
Key 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 and 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.
Participate in internal audits and inspections as a technical support resource.
Job Purpose
To support the technical lifecycle of pharmaceutical products at the site level by assisting in process monitoring, documentation, validation activities (Process and Cleaning Validation), and continuous improvement initiatives. The role contributes to maintaining product quality and compliance through hands-on technical support and collaboration across functions.
Education, Experience & Skills
Pharm-D, B.E, M.Sc Scientific, Technical, Industrial Pharmacy
1–2 years in pharmaceutical manufacturing or technical support roles
To ensure familiarity with GMP, validation practices, and product lifecycle support.
Strong organizational and time-management skills.
Effective communication and collaboration abilities
Key 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 and 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.
Participate in internal audits and inspections as a technical support resource.
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.
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