Site Name: USA - Pennsylvania - King of Prussia
Posted Date: Oct 14 2020
As a Sr Scientist, you will be responsible for building and enhancing biopharmaceutical expertise to be further embedded in the business.
This role will provide YOU the opportunity to lead key activities to progress your career. These responsibilities include some of the following...
Contribute to the implementation of business processes and best working practices to ensure Analytical Lifecycle Management operates as efficiently as possible.
Independently authors internal documents such as reports, protocols, plans or regulatory submissions.
Supports department objectives in alignment with project objectives.
Anticipates and recognizes potential problems, escalates to manager and contributes to actions to solve or prevent problems. High aptitude for learning and applying key learnings to role.
Contribute to the successful and timely transfer, validation and oversight of BioPharm Analytical methods/technologies to and from R&D development, contract manufacturer's, testing labs, or GSK commercial manufacturing organizations (Product Supply Chain).
Effectively prioritizes activities to meet project or department objectives using demonstrable project management skills.
May lead or assist other team members to lead a project, matrix team or small focus groups.
Will support the project team decision making process.
Consistently exhibits professionalism and courtesy and may serve as a representative of GSK to business partners and contract organizations.
Presents effectively to internal R&D and PSC forums and may present results at external meetings.
Keeps manager and matrix team leaders informed of progress and activities.
We are looking for professionals with these required skills to achieve our goals:
If you have the following characteristics, it would be a plus:
Thorough knowledge of cGMP requirements.
Familiar with GLP regulations.
Previous experience in Analytical Technology Transfer and Validation for biopharmaceuticals.
Familiarity with FDA/EU/ICH regulations and guidance particularly as they relate to Analytical Transfer and Validation, Critical Quality Attributes, and Release and Stability Testing.
Independently applies knowledge in area of specialization to assignments that involve multiple decision points.
Our values and expectations are at the heart of everything we do and form an important part of our culture.
These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:
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.
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