Laboratory Lead Analyst – Incoming Materials Ware, England
Job description
Posted Date: Mar 9 2023
The Quality Assurance Department at the GSK Ware manufacturing site ensures that all aspects of the manufacture of products are performed in a controlled manner and meet commitments to international regulatory bodies, as well as the requirements of current Good Manufacturing Practice.
The laboratory teams work as part of the Site Value Streams to ensure that manufactured products are compliant and fit for purpose.
Job Purpose:
The Lead Analyst is a skilled analyst, who takes ownership for providing a proficient service in the analysis of samples and the support of technical investigations/monitoring. Utilising a range of analytical techniques (such as HPLC, GC, UV and Karl Fischer), you will support the laboratory team by providing expert laboratory analysis and effective analytical services for the site to ensure delivery of compliant products to our customers.
The specific responsibilities of the role include assisting the Laboratory Team Leader in overseeing the execution of batch/job testing and release, typically for one testing group. They will also provide guidance and support to the Analysts in the team (enabling efficient batch/job testing and release). You will prepare and check analytical data accurately (according to company, customer and regulatory requirements) and verify the quality and accuracy of analytical results (determining if material meets pre-defined acceptance criteria).
Within your job you will ensure that Good Manufacturing Practice and compliance with EHS regulations in the laboratory are maintained at all times. This will include being responsible for assigned items of Laboratory equipment/instrumentation and troubleshooting (or 5S standards), providing training and coaching in areas of expertise (sharing knowledge and best practices), and taking a lead role in training for New Starters and for Analysts in areas of expertise. Throughout you will also maintain effective working relationships with section, customers and suppliers, and actively contribute to improvement initiatives within the laboratory group (as well as with cross-functional teams).
About You:
This role would suit a driven and motivated individual who has strong knowledge and experience of laboratory testing techniques within intermediate and final products in a GMP (Quality) environment. Strong people skills and a proven ability to work in a team (eg; flexible approach, good communication, planning and organizational skills) are important. You should also have good report writing skills, a strong continuous improvement mindset, and a willingness to work towards standardised and GPS working practices.
About Ware Manufacturing Site:
Medicines at Ware are presented as either Respiratory devices or in Oral Solid Dose form. The site holds a unique position in our network as the only site responsible for launching the company’s pipeline of new medicines in these dose forms, many of which are life saving medicines. A series of investments in new state-of-the-art equipment are being made that will support the delivery of a record number of new products.
CLOSING DATE for applications: Friday 24th of March 2023 (COB).
When applying for this role, please use your CV to describe how you meet the proficiencies for this role.
Basic qualifications:
Relevant qualifications and / or experience.
Competence in current Good Manufacturing Practice (cGMP), understands its impact on their own role and the implications of not following cGMP.
Experience of leading and planning day to day activities for a team.
Experience in root causing of Laboratory Investigations and Deviations.
About GSK:
GSK has changed. In July 2022, we demerged our world-leading consumer healthcare business, Haleon. We are now a fully focused biopharma company. We prioritise innovation in vaccines and specialty medicines, maximising the increasing opportunities to prevent and treat disease. At the heart of this is our R&D focus on the science of the immune system, human genetics and advanced technologies, and our world-leading capabilities in vaccines and medicines development. For more information on GSK please refer to our website: www.gsk.com
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. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.
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 workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, 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*(*US only).
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected] or 0808 234 4391. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels
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