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Gmp Manager Jobs in Georgia (NOW HIRING)

Continuously improve and innovate training execution and management, conducts audits/reviews of ... GMP/Regulatory Requirements • Compliance Trends and Data Integrity • Basic Industrial ...

GMP facility maintenance experience required. * Pay Range : $23.00 per hour to $27.00 per hour ESFM ... In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management ...

Must have a thorough understanding of GMP's, HACCP, SQF systems (Safe Quality Foods), FSMA requirements for human food manufacturing, and USDA requirements for RTE products. Specific Accountabilities:

Must have a thorough understanding of GMP's, HACCP, SQF systems (Safe Quality Foods), FSMA requirements for human food manufacturing, and USDA requirements for RTE products. Specific Accountabilities:

Maintain safety, policies, rules, and regulations as well as Good Manufacturing Practices (GMP's) * Manage the flow of products from the kitchen through the packaging lines to the Warehouse

... of GMP's, HACCP, SQF and USDA requirements and be capable of teaching and enforcing them in the operation on a daily basis. Will also be assisting the Safety Manager for approximately 10 hours each ...

... of GMP's, HACCP, SQF and USDA requirements and be capable of teaching and enforcing them in the operation on a daily basis. Will also be assisting the Safety Manager for approximately 10 hours each ...

... of GMP's, HACCP, SQF and USDA requirements and be capable of teaching and enforcing them in the operation on a daily basis. Will also be assisting the Safety Manager for approximately 10 hours each ...

Manager of Technical Services

Rockmart, GA · On-site

$103K - $103K/yr

... GMP, BRC, Halal, Organic Programs, and any programs affiliated with labeling or product claims ... Manage risk by identifying potential quality or safety issues and implementing corrective actions.

Strong understanding of GMP, cleanroom design, and regulatory environments. * Proven ability to lead cross-functional teams and manage multiple projects simultaneously. * Excellent communication ...

Strong understanding of GMP, cleanroom design, and regulatory environments. * Proven ability to lead cross-functional teams and manage multiple projects simultaneously. * Excellent communication ...

Works closely with QA Manager to ensure food safety standards, GMP?s and HACCP plan are followed at all times by all staffJob Requirements:Basic knowledge of production processes, raw materials ...

Showing results 21-40

Gmp Manager information

See Georgia salary details

$20.7K

$50.3K

$97.9K

How much do gmp manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for gmp manager in Georgia is $50,262.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,500.00 and $57,800.00 per year, depending on experience, location, and employer.

What is a GMP manager?

GMP Managers are professionals responsible for ensuring that manufacturing processes in industries such as pharmaceuticals, biotechnology, and food production comply with Good Manufacturing Practice (GMP) regulations. They oversee quality control, develop and implement standard operating procedures, and conduct internal audits to maintain regulatory standards. Their role is crucial for ensuring that products are consistently produced and controlled according to quality standards, thereby safeguarding consumer health and safety.

What are some common challenges faced by a GMP manager in maintaining regulatory compliance, and how are they typically addressed?

A GMP Manager often encounters challenges such as keeping up with evolving regulatory standards, ensuring consistent staff training, and managing thorough documentation. To address these, managers implement regular training programs, conduct internal audits to identify gaps, and foster a culture of quality across teams. Staying proactive about changes in regulations and collaborating with cross-functional teams helps ensure ongoing compliance and smooth inspections.

What are the key skills and qualifications needed to thrive as a GMP manager, and why are they important?

To thrive as a GMP Manager, you need in-depth knowledge of Good Manufacturing Practices, quality assurance, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit tools, and relevant certifications such as Six Sigma or ISO standards is typically required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills for managing teams and ensuring adherence to regulations. These skills and qualifications ensure product safety, regulatory compliance, and continuous improvement within manufacturing processes.

What is the difference between Gmp Manager vs Quality Assurance Manager?

AspectGmp ManagerQuality Assurance Manager
CertificationsGMP certifications, Quality Management certificationsISO 9001, Quality Management certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingVarious industries including manufacturing, healthcare, and food
Employer & Industry UsageRegulated industries with strict compliance standardsBroadly used across multiple industries for quality oversight
Primary FocusEnsuring compliance with Good Manufacturing PracticesOverseeing overall quality assurance processes

The Gmp Manager primarily focuses on ensuring compliance with Good Manufacturing Practices in regulated industries like pharmaceuticals and biotech. In contrast, the Quality Assurance Manager oversees broader quality assurance processes across various industries. Both roles require similar certifications and work environments but differ in their specific compliance and quality scope.

What are popular job titles related to Gmp Manager jobs in Georgia?

For Gmp Manager jobs in Georgia, the most frequently searched job titles are:

What cities in Georgia are hiring for Gmp Manager jobs?

Cities in Georgia with the most Gmp Manager job openings:

Infographic showing various Gmp Manager job openings in Georgia as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $50,262 per year, or $24.2 per hour.

GMP Training Lead

Marietta, GA • On-site


Zoetis, Inc.
Pharmaceutical and Medicine Manufacturing • 5 - 10K employees

7.7

Company rating: 7.7 out of 10

Based on 79 frontline employees who took The Breakroom Quiz

56th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by students


Full-time

Re-posted 27 days ago


Job description

States considered:
What is it like to work for Zoetis, the world leader in animal health? Zoetis means something a little different to every colleague, but at our core, our purpose 'to nurture the world and humankind by advancing care for animals' is what unites us in all our roles.
We are a global animal health company dedicated to serving veterinarians, livestock producers and people who raise and care for farm and companion animals in more than one hundred countries. And we are excited to become a part of the Lithia Springs, GA, community as we build our newest manufacturing facility to support our growing monoclonal antibody and vaccine portfolios.
We are currently searching for a GMP Training Lead to join our team.
Job Description:
Provide flexible training support across all identified functions, delivering startup-to-full-operations training and assuming responsibility for additional training needs as they arise. This position is the primary trainer for cGMP, cGDP, contamination control and aseptic behavior as it relates to aseptic manufacture of biologic products and materials. Designs, develops and implements curricula, and conducts training for monoclonal antibodies drug product manufacturing, and biologics packaging in compliance with site procedures and global standards. Identify and drive continuous process improvements related to GMP and aseptic training. Continuously improve and innovate training execution and management, conducts audits/reviews of personnel to evaluate training effectiveness. Makes decisions that are in accordance with company policies and SOPs, Core Values, and global regulatory guidelines (including cGMP/cGDP/cGLP), environmental guidelines.
Position Responsibilities:
• Learning Management System administration (SAP SuccessFactors)
• Facilitate New Employee Orientation (including cGMP/cGDP/cGLP), and aseptic training for initial and refresher training for site personnel, including gowning qualification and classroom process simulations.
• Coordinates required annual training requirements with department management
• Conducts spot checks/audits of aseptic techniques and behaviors during operations
• Observes aseptic process simulations (media fills) for aseptic practices and best practices.
• Network with the Global Aseptic Team to share best practices.
• Liaison with colleagues to ensure they are trained and understand the criticality of the aseptic process work they are conducting.
• Coordinates personnel training using available technology, including, but not limited to, virtual reality technology.
• Integrates training sessions and training documentation into electronic training document management systems.
• Collaborate with area Operations Team Leaders to train and lead colleagues in the performance of best practices.
• Collaborate with QC to analyze training techniques and instructions for error prone testing
• Collaborate with QA to analyze training techniques and instructions for incidents with patterns and trends
• Utilize subject matter knowledge related to Aseptic Processing in the conduct of training:
o GMP/Regulatory Requirements
• Compliance Trends and Data Integrity
• Basic Industrial Microbiology
• Types of Microorganisms
• Growth and Reproduction
• Sources of Cleanroom Contamination
• Reduction/Elimination
• Measurement Systems
• Site Specific Data Trends and Metrics
o Facility Design / Environmental Controls
• Cleaning and Disinfection (facility surfaces, equipment)
• Aseptic and Controlled Area Gowning
• Aseptic Training / Good Aseptic Technique
• Material Transfer
• Material/Personnel / Equipment Flow and Movement
• Use of Isolator and Barrier Systems
• Sterilization / Validation
• Bioburden Reduction
Education and Experience:
• Bachelor's degree in Training & Development, Instructional Design, Adult Education, Organizational Development, Learning & Development, or Engineering, Biology, Chemistry, Microbiology, Virology, Immunology.
• Minimum of 5+ years of experience in training delivery, training coordination, curriculum development, learning and development, or related training functions, including demonstrated classroom facilitation and presentation experience.
Technical Skills Requirements:
• Must have strong technical/analytical skills and possess a high degree of personal motivation.
• Excellent interpersonal skills and ability to interact across divisional boundaries.
• Familiar/proficient in adult learning methodologies
• Strong technical writing skills.
• Preferred experience in aseptic and biological product formulation (blend/fill/lyophilization), packaging, and/or testing.
• A working knowledge of vaccine production methods and experimental design and experience in GLP or cGMP.
• Knowledge of FDA, APHIS, VMD, USDA regulations applicable to the Pharmaceutical/Biological industry.
• Preferred experience in Lean/Six Sigma
Physical Requirements:
• Must be able to walk or stand for long periods of time.
• Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.
• Must be able to work scheduled 40 hours with the ability to work overtime as needed.
• Frequent lifting and carrying of 5 to 25 lbs.
• Regular reaching, bending, stooping, and twisting
• Repetitive motion and substantial movement of the wrists, hands, and/or fingers
• Able to become qualified to enter clean room environments
• Work Environment: While performing the duties of this job, the employee occasionally works in clean room environments. The noise of these work environments is typical office noise.
Full time
Regular
Colleague
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn, including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from @zoetis.com, please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.


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