The Manufacturing Associate will perform duties as assigned with respect to quality, timeliness, quantity, and cost. Work individually and as a team to deliver cGMP compliant product.

Adhere to GSK policies, procedures, and support site goals. Complete documentation in line with regulatory, GSK, and departmental requirements.

Work and communicate closely with other departments both inside and outside of MPL Manufacturing. Train and mentor less experienced staff.

Work with minimal supervision and coordinate complex tasks between departments. Oversee and coordinate equipment related task and issues.

Demonstrate ability to cross train in multiple disciplines across MPL Manufacturing and participate in cross functional teams.

Demonstrates an in-depth knowledge of the job.

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

2nd Shift Schedule :

Monday / Tuesday / Wednesday / Thursday 4 : 00pm - 3 : 00am (with a 10% shift pay differential)

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. Hazardous waste training depending on specific requirements of 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.

• Participate in and support continuous improvement and LEAN initiatives. Recognize technical issues and relay to supervisor.
• 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.

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 GED
• 1 year(s) of cGMP / healthcare / lab related experience

Preferred Qualifications :

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

• Bachelor's degree or some post-secondary education
• Knowledge of a controlled, clean environment
• Good written and verbal skills
• Ability to maintain attention to detail while executing multiple tasks with minimal supervision
• Ability to work in a manufacturing and open office environment
• Understanding of weights and volume measurements
• Able to work independently and in a team environment
• Understanding of weights and volume measures as well as a general knowledge of bioburden control techniques.
• Ability to take initiative and prioritize tasks, good time management, problem prevention, and problem-solving skills Strong understanding of cGMP and quality systems.
• Strong understanding of Quality systems to include deviation and CAPA systems
• Understanding of Microsoft Office (MS Word, MS Excel, MS Outlook)

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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.

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.

Last updated : 2024-05-24