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Gmp Manufacturing Jobs in Georgia (NOW HIRING)

Within Global Engineering, the Project Director has overall responsibility for driving large, complex projects to successful completion in support of GMP manufacturing operations. As leader, the ...

New

Read, understand, and follow Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) * Prepare QA line clearances and support production line readiness * Communicate production ...

Read, understand, and follow Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) * Prepare QA line clearances and support production line readiness * Communicate production ...

This role is a valuable part of Roche's Global Engineering team within Pharma Technical Operations, which is committed to delivering world-class capital projects that enable our GMP manufacturing ...

Read, understand, and follow Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) * Prepare QA line clearances and support production line readiness * Communicate production ...

GMP Training Lead

Atlanta, GA · On-site

$110 - $160/hr

## GMP Training LeadApplylocations: Atlantatime type: Full timeposted on: Posted Todayjob requisition ... manufacturing facility to support our growing monoclonal antibody and vaccine portfolios.We are ...

Senior MES MBR Author

Atlanta, GA · On-site

$125 - $135/hr

Ensure eMBR design, implementation, and maintenance comply with GMP requirements and site data integrity standards. * Provide hands‑on manufacturing support, end‑user training, troubleshooting ...

New

... manufacturing facility to support our growing monoclonal antibody and vaccine portfolios. We are ... Identify and drive continuous process improvements related to GMP and aseptic training.

... manufacturing facility to support our growing monoclonal antibody and vaccine portfolios. We are ... Identify and drive continuous process improvements related to GMP and aseptic training.

... manufacturing facility to support our growing monoclonal antibody and vaccine portfolios. We are ... Identify and drive continuous process improvements related to GMP and aseptic training.

Packaging Technician I

Athens, GA · On-site

$15 - $20/hr

Skills: * GMP. * Manufacturing production experience. Education and Experience: * High School Diploma or GED. Benefits Our Benefits Include: * Medical, Dental, and Vision Insurance * 401(k) ...

Manufacturing Supervisor

Adel, GA · On-site

$50K - $68K/yr

Manufacturing Manager FLSA Status: Exempt, Salary Location: Adel, GA POSITION SUMMARY We are ... Establish and maintain compliance to current GMP, safety programs * Communicate any safety issues ...

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Gmp Manufacturing information

See Georgia salary details

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How much do gmp manufacturing jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for gmp manufacturing in Georgia is $21.06, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $24.38 per hour, depending on experience, location, and employer.

What is a GMP manufacturing?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

What are the key skills and qualifications needed to thrive in GMP manufacturing?

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

What job categories do people searching Gmp Manufacturing jobs in Georgia look for?

The top searched job categories for Gmp Manufacturing jobs in Georgia are:

What cities in Georgia are hiring for Gmp Manufacturing jobs?

Cities in Georgia with the most Gmp Manufacturing job openings:

Infographic showing various Gmp Manufacturing job openings in Georgia as of August 2026, with employment types broken down into 82% Full Time, 6% Part Time, 7% Contract, and 5% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $43,815 per year, or $21.1 per hour.

Remote GMP Quality Mgr

Globalchannelmanagement

Atlanta, GA • Remote

Full-time

Posted 3 days ago

New


Job description

Remote GMP Quality Mgr needs 8+ years of experience required, with relevant experience in biotech or pharmaceutical industry with most experience in a Quality role.

Advanced knowledge of GMP manufacturing and/or market release of pharmaceutical dosage forms and/or combination products.

Experience with managing external CMOs, contract laboratories, and third-party logistics suppliers.

Must have experience in reviewing and approving master and executed batch records and performing final disposition of drug substances and products.

Experience managing quality events (investigations, CAPA and change control), and working knowledge of formal risk management tools and assessments. The individual must demonstrate the ability to evaluate and assess technically complex quality events, as well as the ability to document these events with excellent technical writing skills.

Experience in evolving GMP related quality systems, policies, and procedures to ensure compliance with evolving standards as well as improving the efficiency of related workflows.

Strong ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations.

Excellent verbal and written communication skills, including ability to interact effectively with senior management, partners, and project core team members.

Self-motivated, flexible, and able to prioritize work and handle multiple assignments in a fast-paced environment, while maintaining a high level of quality and compliance.

Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or relevant field of study.

Duties:

Be the QA representative on cross-functional project teams. Responsible for communicating with the Quality and Production departments at domestic and international contract manufacturing organizations, and within SMPA's Quality, Supply Chain, CMC, and Commercial Manufacturing departments.

Conducts product release activities for clinical and commercial drug substances and drug products; including review and approval of Master Batch Records, Executed Batch Records, release and stability testing documentation, and batch disposition. These activities must be conducted in a timely manner to ensure continued product supply while ensuring Quality and Safety of the product.


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About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

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