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For Companies At a Glance
- Tasks: Ensure compliance with quality standards and support timely release of medicines.
- Company: GSK is a global healthcare leader dedicated to improving health for billions.
- Benefits: Enjoy a collaborative environment, opportunities for growth, and a focus on wellbeing.
- Why this job: Join a mission-driven team transforming medical research and making a real impact.
- Qualifications: Bachelor's in Science or equivalent experience; background in regulated environments preferred.
- Other info: GSK values diversity and inclusion, welcoming all qualified applicants.
The predicted salary is between 36000 - 60000 £ per year.
Overview
GlaxoSmithKline (GSK) is a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We are on an audacious journey to impact the health of 2.5 billion people over the next decade. Our R&D division is at the forefront of this mission, dedicated to the discovery and development of groundbreaking vaccines and medicines. We are transforming the landscape of medical research by integrating cutting-edge science and technology and harnessing the power of genetics and new data. By fostering a collaborative environment that unites the talents of our people, we are revolutionizing R&D to pre-empt and defeat diseases. Join us in our commitment to uniting science, technology, and talent to get ahead of disease together.
Position Summary
GSK are the lookout for a Biopharmaceuticals Testing Laboratory (BioCTL) QA Specialist to join the team in Stevenage. This person will ensure that the BioCTL complies with all QMS and relevant regulatory standards in relation to data generation and laboratory testing and approval.
Key Responsibilities
- Review, approve and issue QC data to support timely release of medicines to the market.
- Provide coaching and support to improve Right First Time performance.
- Perform document control activities, including controlled printing, reconciliation and archiving.
- Assist in the preparation for and participation in inspections and audits.
- Author GMP documents.
- Initiate and participate in quality events such as deviation investigations and change controls.
- Participate in GEMBA and process confirmations of quality systems and processes to improve compliance and efficiency.
Minimum Requirements/Skills
- Bachelor of Science or equivalent work experience.
- Background in Science, Engineering or other technical discipline.
- Ability to interpret complex data and draw conclusions about scientific and technical data.
- Experience working in a regulated environment, preferably in a GMP environment in a role directly related or supporting Quality or Manufacturing.
- Competency in Microsoft Office.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
Inclusion at GSK
GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
If you need any adjustments in the recruitment process, please get in touch with our Recruitment team ( ) to further discuss this today.
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 GSK’s Transparency Reporting For the Record site.
QA Specialist employer: Allegis Global Solutions
Contact Detail:
Allegis Global Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Specialist
✨Tip Number 1
Familiarise yourself with GSK's mission and values. Understanding their commitment to health and innovation will help you align your responses during interviews, showcasing how your personal values resonate with theirs.
✨Tip Number 2
Brush up on your knowledge of Good Manufacturing Practices (GMP) and quality management systems. Being able to discuss specific examples of how you've applied these in previous roles will demonstrate your expertise and readiness for the QA Specialist position.
✨Tip Number 3
Network with current or former GSK employees on platforms like LinkedIn. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during your interview.
✨Tip Number 4
Prepare for potential technical questions related to data interpretation and quality assurance processes. Practising how to articulate your thought process when analysing complex data will help you stand out as a candidate.
We think you need these skills to ace QA Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a QA Specialist at GSK. Familiarise yourself with their commitment to quality management systems (QMS) and regulatory standards.
Tailor Your CV: Highlight your relevant experience in quality assurance, particularly in regulated environments like GMP. Emphasise your ability to interpret complex data and any specific achievements that demonstrate your skills.
Craft a Compelling Cover Letter: In your cover letter, express your passion for the role and how your background aligns with GSK's mission. Mention your understanding of their focus on science and technology in healthcare and how you can contribute to their goals.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no spelling or grammatical errors, and that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at Allegis Global Solutions
✨Understand GSK's Mission
Before your interview, take some time to research GSK's mission and values. Understanding their commitment to improving health globally will help you align your answers with their goals and demonstrate your enthusiasm for the role.
✨Showcase Your Regulatory Knowledge
As a QA Specialist, familiarity with regulatory standards is crucial. Be prepared to discuss your experience in regulated environments, particularly in GMP settings, and how you've ensured compliance in past roles.
✨Prepare for Technical Questions
Expect questions that assess your ability to interpret complex data and draw conclusions. Brush up on relevant scientific concepts and be ready to provide examples of how you've applied this knowledge in your previous work.
✨Demonstrate Team Collaboration Skills
GSK values collaboration, so be ready to share examples of how you've worked effectively within a team. Highlight any experiences where you provided coaching or support to colleagues, as this aligns with the responsibilities of the role.
