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Please note this position may be for current hiring needs as well as pipelining potential talent for future vacancies. Communication may be limited until we have initiated an official recruitment process for this position. We appreciate your patience and hope to be in contact soon.

Shift Schedules (subject to change based on business needs):

2nd Shift -- Schedule:

• Monday/Tuesday/Wednesday/Thursday -- 4:00pm - 3:00am

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

• Responsible for application of GSK safety and environmental guidelines and act as a role model within the department. Ensure all job responsibilities are in compliance with applicable regulations, current operating procedures, and industry practice. Identify and help mitigate EHS and safety risks. Work with supervisor to mitigate safety concerns and provide guidance for teammates related to safety topics. Hazardous waste training depending on specific requirements of the VS department.
• Ensure all activities are executed following quality and regulatory standards. Supports cross-functional communication and the GSK quality mindset by proactively identifying and reporting compliance issues to area supervisor or QA. Work with supervisor and QA to mitigate identified issues. Adhere to all GSK QMS policies and procedures applicable to functional area. Lead and facilitate the inspection readiness of the department.
• Participate in and support continuous improvement and LEAN initiatives. Recognize technical issues and relay to supervisor. Drive and champion LEAN behaviors within the team.
• Represent GSK with the highest level of integrity and professionalism. Ability to maintain confidentiality of sensitive information. Adhere to GSK policies and procedures and support management decisions and goals in a professional manner. Show awareness of changing schedules, request and priorities put forth by management. Hold self and teammates to applicable safety and quality standards. Support cross-functional communication both within and external to the department. Meet agreed timelines for task and escalate timeline adherence concerns to supervisor. Assist in and allocate time for other team members to complete assigned tasks.
• Support production planning to achieve VS objectives, including delivery to yearly manufacturing plan. Assist supervisor in setting, monitoring, and achieving area objectives, metrics, and targets.
• The following GSK values and expectations are key behavioral characteristics for this role: Patient Focus, Transparency, Respect, and Integrity, Courage, Accountability, Development, and Teamwork

Why you?

Basic Qualifications:

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

• High School Diploma or equivalent
• 3+ years of cGMP/healthcare/lab related experience

Preferred Qualifications:

• Bachelor's Degree in Technical/Science field
• Good verbal and written communication skills
• Ability to communicate effectively and project a professional image when giving/taking information in person, in writing, or over the phone
• Understanding of Microsoft Office (MS Word, MS Excel, MS Outlook)
• Ability to take initiative and prioritize tasks, good time management, problem prevention, and problem-solving skills
• Exhibit leadership capabilities (e.g., influence, enable and drive change, and continuous improvement)
• Strong understanding of cGMP and quality systems including the ability to guide others in correct cGMP principles
• Strong understanding of Quality systems to include deviation and CAPA systems
• Working understanding of SAP requirements related to area specific functions and ability to direct team members in the correct use of SAP

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