Associate Quality Management Systems Specialist - Athens, GA

Meissner; Athens (GA); Presencial; USD 68.000 - 87.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Full Medical, Dental and Vision with H

HSA Employer Contributions

HQ Onsite Gym

Coffee bars

Free EV charging

Employee discounts

401k and Profit Sharing

Company Sponsored Life Insurance

Employee Assistance Program

Paid Time Off & Holidays

Descripción de la vacante

Meissner is seeking an Associate Quality Management Systems Specialist in Athens, GA. The role focuses on maintaining and improving the Quality Management System to ensure cGMP compliance and client requirements.

You will support document control, CAPA, deviations, and audit readiness while collaborating with Commercial and Technical Operations teams. The position emphasizes attention to detail and cross-functional communication in a fast-paced pharma environment.

Formación

• 2+ years of experience in a Quality Assurance role within pharma/biotech.
• Bachelor’s degree in a scientific/engineering discipline preferred.
• Working knowledge of cGMP regulations and quality systems (CAPA, deviations, OOS, document control).
• Experience with electronic Quality Management Systems (eQMS) or document management systems preferred.
• Strong attention to detail with ability to review GMP documentation for accuracy and compliance.
• Ability to manage multiple priorities in a fast-paced, regulated environment.
• Excellent written and verbal communication, cross-functional collaboration.

Responsabilidades

• Maintain and improve the Quality Management System to ensure cGMP compliance.
• Provide QA SME support across document control, CAPA, deviations and audits.
• Track metrics, perform system administration, and support continuous improvement.
• Assist with internal and external audits and readiness activities.
• Oversee document control processes and electronic documentation system usage.
• Ensure regulatory documentation and SOPs meet requirements.
• Review testing and log documentation for compliance and traceability.

Conocimientos

Quality Assurance

cGMP knowledge

Document control

CAPA

Deviations

Audit readiness

Interdepartmental comms

Educación

Bachelor's degree in science or engineering

Herramientas

eQMS

Document management system

Descripción del empleo

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Associate Quality Management Systems Specialist - Athens, GA

If your idea of a great day includes keeping systems organized, records accurate, and quality standards on point, this could be the role for you. If you’ve got a sharp eye for detail and a knack for keeping things on track, this QMS role is a great way to make quality count.

Join a team where your love of order, process, and precision helps keep quality running smoothly behind the scenes.

Who is Meissner?

The goal at Meissner is to be more than simply good; it is to be extraordinary. Extraordinary performance comes from extraordinary people.

Meissner as a group is passionate about helping our clients manufacture lifesaving and life enhancing drugs, therapies, and vaccines. We develop, manufacture, supply and service advanced microfiltration products and single-use systems worldwide.

We know that when you are passionate about what you do, it’s more than just a job.

Meissner is focused on the development of the whole individual, and we have programs and tools in place to help us stay at our best mentally and physically. In alignment with our commitment to support the growth and development of the whole individual, Meissner has inaugurated a Learning and Development department to solely focus on cultivating our team. When you grow, we grow.

How you will make an impact:

The Associate Quality Management Systems (QMS) Specialist plays a key role in maintaining and improving the Quality Management System to ensure compliance with cGMP regulations and client requirements. This position provides Quality subject matter expertise across document control, CAPA, deviations, and audit readiness, partnering cross-functionally with Commercial and Technical Operations teams. The role is responsible for supporting QMS performance through metrics tracking, system administration, and continuous improvement efforts that enable the consistent delivery of safe and effective pharmaceutical products.

• Collaborate as a solution-oriented team member to work alongside the Commercial and Technical operations teams, delivering QA objectives to support business growth.
• Track and report metrics and key performance indicators for the Quality Management System.
• Monitor and follow-up on open actions related to Corrective and Preventative Actions (CAPA), Out of Specification (OOS) reports and Deviations.
• Assist with preparations for internal and external audits, including documentation readiness, traceability, and response to findings.
• Oversee document control processes, including creation, revision, distribution, and archival of SOPs, work instructions, and quality records. Administer the electronic document management system, including user access, training, workflows, and maintenance.
• Ensure documentation compliance with applicable regulations (cGMP) and internal and Quality procedures.
• Review routine testing, monitoring, and log documentation for compliance.
• Track document lifecycle milestones and completion.

This is an on-site role based out of our facility in Athens, GA.

The skills and experience you’ll need:

• 2+ years of experience in a Quality Assurance role within the pharmaceutical or biotechnology industry. Relevant internship or co-op experience considered.
• Bachelor’s degree in a scientific, engineering, or related discipline preferred.
• Working knowledge of cGMP regulations and quality systems, including CAPA, deviations, OOS investigations, and document control.
• Experience with electronic Quality Management Systems (eQMS) or document management systems is preferred.
• Strong attention to detail with the ability to review and assess GMP documentation for accuracy and compliance.
• Ability to manage multiple priorities in a fast-paced, regulated environment.
• Effective written and verbal communication skills, with experience interacting cross-functionally and with external clients.
• Demonstrated ability to work both independently and collaboratively within a team environment.

What we can offer you:

• Full Medical, Dental and Vision coverage with HSA Employer Contributions for eligible plans
• Additional Perks- HQ Onsite Full Gym, Ultramodern Coffee Bars, Free EV Charging Stations, Employee Discounts
• 401k, Profit Sharing, 401k Advisory Services
• Company Sponsored Life Insurance
• Employee Assistance Program
• Paid Time Off, Paid Holidays, Anniversary Holiday

Meissner is proud to be an Equal Opportunity Employer.

US BASE PAY SCALE $68,000 - $87,400

The base pay scale for this role is what Meissner reasonably expects to pay for the position although actual pay may vary from this scale depending on an applicant's experience.