Are you seeking an opportunity where you can grow your technical expertise on pharmaceutical analysis and development? If so, this Senior Analytical Scientist role is an exciting prospect to explore.
As a Senior Analytical Scientist, you will progress analytical aspects of projects, utilizing your technical expertise as part of a product development team working with many partner groups.
This role will provide YOU the opportunity to contribute to analytical development and to progress YOUR career. Your responsibilities include some of the following:
- Performs GMP analytical testing to support release or rejection of starting materials, synthetic intermediates and active pharmaceutical ingredients, as well as formulation intermediate, bulk and finished drug products.
- With supervision, executes method validation experiments for starting materials, synthetic intermediates, drug substances and drug products appropriate to clinical development phases and in line with QbD approaches.
- Documents laboratory work in accordance with GxP expectations, company policy, and legal requirements.
- Review of experiments, stability protocols, and other key documents
- Writes specific technical sections of internal and external reports with supervision.
- Performs routine data management tasks including recording results effectively in a laboratory notebook or computer independently (e.g., tabulating and graphing results).
- Identifies and troubleshoots any problems in the execution of experimental processes; interprets results and communicates them to his/her supervisor.
- Prepares and communicates conclusions and recommendations for next steps to relevant members of own team or Matrix Teams.
- Provides scientific input and recommendations to the project team decision making process.
- Follows safety requirements for his/her laboratory/working environment
- BS in Chemistry with 5+ years of relevant experience, or MS in Chemistry with 3+ years of relevant experience, or PhD with no industry experience.
- Demonstrated technical expertise and working familiarity with several analytical techniques, and laboratory procedures.
- Knowledge of how to analyze and interpret experimental data.
- Knowledge of cGMP requirements
- Awareness with FDA/EU/UK and ICH regulations and guidances related to analytical transfer and validation and release and stability testing.
- Experience with laboratory systems (e.g. Waters Empower CDS and Labware)
- Experience with both small molecule and biopharm analytical development.
- Good technical writing skills for documentation.
- Collaborates well with others in the group and across groups.
At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader inConsumer Health, strengthening our leadership, and transforming our commercial execution. Now, we're making the biggestchanges we've made to our business in over 20 years.We're on track to separate and create two new companies in 2022:
New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and geneticsscience; and a new world-leading consumer healthcare company of loved and trusted brands.
With new ambition comes new purpose. For New GSK, this is to unite science, talent and technology to get ahead of diseasetogether - all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; andas a new GSK where outstanding people thrive.
Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culturethat isambitious for patients
- so we deliver what matters better and faster;accountable for impact
- with clear ownership ofgoals and support to succeed; andwhere we do the right thing
. So, if you're ready to improve the lives of billions, join us at thisexciting moment in our journey. Join our challenge to get Ahead Together.
- Operating at pace and agile decision-making - using evidence and applying judgement to balance pace, rigour and risk.
- Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
- Continuously looking for opportunities to learn, build skills and share learning.
- Sustaining energy and well-being
- Building strong relationships and collaboration, honest and open conversations.
- Budgeting and cost-consciousness
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that 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.
At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve.
GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons.
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