Career Conversion Programme Quality Validation Officer

Job description

Overview
The Career Conversion Programme (CCP) (Train-and-Place with Commitment to Hire) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore’s biopharmaceuticals manufacturing industry in anticipation of hiring demand.


The training programme consists of 15 months of local attachment with GSK.

Due to the nature of the programme, we can only consider Singapore Citizens and Singapore Permanent Residents.

Training allowances are CPF exempted.


For more information, please visit
Career Conversion Programmes (CCP) for Individuals
Role Description
This position reports to the Technical, Quality & Validation Manager and supports key quality operations at the site.


Trainee Responsibilities
To ensure that products manufactured are in full compliance with current Good Manufacturing Practices (cGMP) and regulatory requirements so as to meet stipulated product quality standards in line with the established specifications of the organization.


Draft, compile, review and update appropriate policies and procedures in support of the validation activities on site
Assess, review and approve changes that may have an impact on the product quality, regulatory and validation status of the facility, processes, method validation or systems on site
Ensure that validation review of systems or processes are conducted on a periodic basis to ensure that the validation status is maintained, make recommendations for re-validation as required, pending outcome of the validation review, and approve Continued Process Verification (CPV) documents
Assess, review and approve changes that may have an impact on product quality, validation and/or cGMP compliance.

Upon implementation of changes, review and ensure proper closure of changes
Education / Licenses
Degree in Chemical Engineering, Chemistry or related fields
Competencies / Skills
Develop logical thinking skills through active participation in change controls and quality decisions
Develop oral and written communication skills
Engaging stakeholders, customers and suppliers professionally
Gain experience with online system used for change controls
Gain extensive knowledge on GMP, validation, quality and manufacturing processes
Gain understanding of regulatory processes
Gain exposure to internal audits (as auditee)
Location
You will be based at one of our manufacturing sites in Singapore near Jurong.


How to Apply
Applications are now open.

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We recommend you apply as soon as possible, because we accept ongoing applications and offer positions on a first come, first served basis!
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We strive to make our recruitment process free of bias of any kind and aim to create an inclusive workplace at GSK.

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Why GSK?
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.


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Required Skill Profession

Other General