Are you looking for an opportunity to support a Quality Management team in the day to day operations in a manufacturing environment? If so, this is the role for you.

As Environmental Monitor, you will be responsible for the collection of environmental monitoring samples and identifying deviations and potential problems and communicating these situations with appropriate personnel.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Perform Environmental Monitoring duties related to viable air, viable surfaces, swabs, and non-viable air sample collection.
• Coordination of daily sampling activities for environmental monitoring (including generation of sample collection paperwork, labels, sample submission, etc) to meet SOP requirements.
• Responsible for maintaining and ordering sufficient supplies, maintain EM media inventories, ordering equipment to perform all monitoring, and maintaining the equipment in good working conditions in a calibrated status.
• Handle special projects such as abnormal test results, validation studies as needed.
• Assure that all required documentation including records and logs, is complete and accurate according to the current GMP rules.
• Maintain required records and logs.
• Revise and write SOP's specific to monitoring as required and assist/lead the training of new personnel.
• Assist with and participate in development of training programs and conduct training sessions for new and less experienced staff as necessary.
• When assigned to rotating shift work; work independently and without direct supervision to perform normal operating routines and emergency response procedures.
• Communicate and report status of operations as well as variances from specifications to area manager. Take appropriate actions and escalate issues immediately.
• Perform all job responsibilities in compliance with applicable EHS and GMP regulations, guidelines, policies, GSK standard operating & safety procedures, and industry practice and Industrial Excellence initiatives.

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

• Bachelor's degree

OR

• HS diploma and 5 years of experience in quality control or production within the pharmaceutical or biotechnology industry

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

• 2 years of experience in quality control or production within the pharmaceutical or biotechnology industry preferred
• Knowledge of standard aseptic technique.
• Must meet the Office of Health & Safety (OHS) Medical Guidance for working in production environment.
• Computer skills required in Excel and Word.
• Ability to follow written procedures and document results in a neat and precise manner.
• Position may require employees to work in a 24/7 rotational schedule. This schedule will include holidays, and weekends; over-time may be required.
• Must be well organized, flexible, open-minded and dynamic.
• Must have demonstrated self-direct work habits and strong communication skills.
• Must be a committed team player prepared to work in and embrace a team based culture.
• Ability to work within a multi-skilled team.
• Maintain attention to detail, while completing multiple or repetitive tasks.
• Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines.
• Maintain a high level of integrity while balancing multiple priorities and responsibilities.
• Some experience in analytical systems including quality control/production, validation, documentation and compliance preferred.
• Experience with SAP system
• Strong interpersonal skills. Solid team player able to function within team based organization.
• Able to interact with peers, subordinates and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production and QA and QC.
• Able to prioritize and decide appropriate course of actions.
• Ability to understand client's needs (producers) and to interact with people from various domains (Regulatory, QA, other analytical groups inside the Company.)
• Demonstrated familiarity with cGMP's, facility regulatory guidelines and standard operating procedures.

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Please visit to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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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