Reg Associate Manager I
2 weeks ago
Business Introduction
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
Independently and confidently executes agreed dossier strategy.
Minimum of 5 years of experience in CMC
Bachelor's degree in Chemistry, pharmacy or other related science or technical bachelor's degree.
Independently manages multiple BioPharm project assignments simultaneously; assignments will range in complexity, but more complex work is expected.
Independently completes data assessment to ensure dossier is fit for purpose.
Identifies risks associated with submission data and information packages.
Escalates issues with line manager that have business impact.
May act as reviewer/approver for dossiers prepared by peers and identifies improvement opportunities for Regulatory processes, policies and systems.
Understands regulations, guidelines, procedures and policies relating to registration and manufacturing of pharmaceutical products, to expedite submission, review and approval of global applications. May provide consultation and solutions being the subject matter expert in specific areas of expertise. Acts as mentor/trainer for new staff.
Understands internal/external Regulatory environment.
Actively builds an organizational network (GSC, LOC, PO and other relevant stakeholders), promotes and is engaged in knowledge and experience sharing.
Communicates across GSK, as necessary regarding project and policy issues ensuring optimum position for GSK
Preferred Qualification
If you have the following characteristics, it would be a plus:
Broad understanding of the pharmaceutical industry, drug development environment, and R&D processes and objectives.
Global Regulatory submission experience - Knowledge of regulatory agency guidelines
Excellent organizational skills, attention to detail and commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines
Excellent written and verbal communication skills and ability to present information in a clear and concise manner
Ability to interpret and advise on guidelines and requirements on a global basis, reflecting recent GSK experience
Ability to build effective working relationships and work in a matrix environment effectively
Ability to think flexibly in order to meet constantly shifting priorities and timelines
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.
Inclusion at GSK:
As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.
Please contact our Recruitment Team at IN.recruitment- to discuss your needs.
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.
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