1+ months

Investigator, Analytical Lifecycle Management

GSK
King of Prussia, PA 19406
Site Name: USA - Pennsylvania - King of Prussia
Posted Date: Sep 17 2020

As an Investigator - Analytical Lifecycle Management, 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 strategically and as efficiently as possible.
  • Independently authors internal reports, protocols, policies/plans or regulatory submissions.
  • Supports department objectives in alignment with project objectives.
  • Anticipates and recognizes potential problems, initiates actions to solve or prevent problems and communicates issues/risks to project lead and manager.
  • Contribute to the successful and timely transfer, validation and oversight of BioPharm Analytical methods/technologies to and from R&D development, contract manufacturers, 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 a project, matrix team or small focus groups.
  • Plays a significant part in 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

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Bachelors degree in Biochemistry, Chemistry or Biology and at least 5 years Analytical Technology Transfer and Validation experience OR a Ph.D./MS degree in Biochemistry, Chemistry or Biology and at least 3 years Analytical Technology Transfer and Validation experience

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Thorough knowledge of cGMP requirements.
  • 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.
  • Familiar with GLP regulations.
  • Previous Biopharmaceutical experience.

Why GSK?

Our values and expectationsare 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.

*This is a job description to aide in the job posting, but does not include all job evaluation details.

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.

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 GSKs compliance to all federal and state US Transparency requirements. For more information, please visit GSKs Transparency Reporting For the Record site.

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Posted: 2020-09-18 Expires: 2020-12-18

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Investigator, Analytical Lifecycle Management

GSK
King of Prussia, PA 19406

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