Analytical Chemistry Investigator

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Location :
Upper Providence, Pennsylvania

Expiry Date :
Tue, 15 Jun 2021 23:59:59 GMT

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Description :
Are you looking for a collaborative analytical chemist role that allows you to contribute to scientific strategy and accelerate Pharmaceutical Research and Development? If so, this role could be an ideal opportunity to explore. As an Investigator, you will design and perform quantitative and/or qualitative analysis using classical and instrumental methods to support API process development. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: – To progress analytical aspects of projects utilising their substantial experience and expertise as part of a CMC Analytical team and wider matrix teams, plus any other tasks as requested by team leader or departmental director. – Development and validation of robust analytical methods for drug substance and drug product. – Produce and interpret data to support the release and stability testing of drug substance and drug product. – Review of experiments, stability protocols, and other key documents – Contribute and support departmental cross-training activities on analytical techniques used for analysis of biopharm molecules. – May directly supervise GSK staff within the department – Independently writes and edits sections for patents or regulatory submissions, authors scientific papers and internal reports. – Perform/Supervise appropriate Quality Control activities, including- – Performing analytical testing to support release or rejection of starting materials, intermediates and active pharmaceutical ingredients, intermediate, bulk and finished drug products by Quality Assurance Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: – BS with 5+ years experience /MS with 3+ years Chemistry/ PhD with 1+ year experience – 3+ years experience leading Analytical Chemistry aspects of R & D projects (including, but not limited to Method transfer, Quality Control, Regulatory Filing, Method Development and Validation) Preferred Qualifications: If you have the following characteristics, it would be a plus: – Expertise in analytical chemistry is preferred – GMP requirements and SOPs is preferred – Experience with regulatory requirements and the drug development process preferred – Analytical Quality by Design approaches preferred – Experience working with External partners preferred 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 *LI-GSK If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1- (US Toll Free) or +1 (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.