Site Name: Guayama JV Posted Date: Nov 22 2021 In this role you will have the opportunity to accomplish projects, studies, investigations, reports and document reviews independently. Maintains expertise in an area develops understanding of the Quality program and expands into related fields. Evaluates and defines appropriate approaches, including those that are less familiar, for the achievement of project goals. Involves innovation and creativity within the existing methodologies in the development and completion of assigned projects. Continues to build credibility, giving significant intellectual and technical advice. Builds respect within the Company with high quality work reflected in excellent presentations and the successful completion of projects. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Independently designs, executes, interprets and reports results on technical nature. Is expected to solve most problems that arise with little supervisory input. Has the ability to assess some technical risk. Effectively communicates results of own work at meetings or in presentations. Demonstrates willingness to assist others with problems. Has the confidence and technical knowledge to mentor laboratory staff. Establishes him/herself as a resource on technical matters. Continues to build and maintain credibility within the group by performing high quality work. Makes important intellectual or technical contributions affecting the direction of the group. Makes independent contributions to the development of new technologies. Develops and revises test methods, specifications and procedures in compliance with applicable regulations; carries out technical and administrative duties as assigned. Accountable for development, validation and troubleshooting of existing and new test methods. Participates in the lab qualification of new or improved test methods for marketed product or raw materials. Conducts or participates in laboratory investigations as required. Generates and revises SOPs, change controls and deviation investigations as needed. Accountable for the annual reports pertaining to their area of responsibility (e.g. environmental monitoring, laboratory investigations, etc.). Contributor to Annual Product Reports as requested. Ensures that any waste generated as part of his/her responsibilities is handled in compliance with applicable environmental regulations and in accordance to establish SOP's for handling waste. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: B.S. in Chemistry or Microbiology with MS desired. 5 + years of experience within the Pharmaceutical industry. Preferred Qualifications: If you have the following characteristics, it would be a plus: MS is Analytical Chemistry or Microbiology, PhD preferred. Why GSK? 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. *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. At GSK, the health and safety of our employees are of paramount importance. 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