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Pharmaceutical Engineer Jobs in Georgia (NOW HIRING)

Electrical Engineer

Norcross, GA · On-site

$80K - $120K/yr

  • Medical

  • Dental

  • Life

MURZAN INC. A food processing and pharmaceutical and engineering and equipment manufacturer is seeking for a Graduated Electrical Engineer for our plant in Norcross, Georgia. Company Description ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the ...

Jedson Engineering is an Engineering Consultancy headquartered in Cincinnati, OH. We provide full ... or pharmaceutical industries. Some travel to project and construction sites will be required.

Jedson Engineering is an Engineering Consultancy headquartered in Cincinnati, OH. We provide full ... or pharmaceutical industries. Some travel to project and construction sites will be required.

Senior Mechanical Engineer

Marietta, GA · On-site

$94K - $125K/yr

Will function as a hands-on engineer providing process and packaging engineering expertise for ... Industries may include foods, pharmaceutical, pulp and paper, chemical & other industries. Be ...

Senior Mechanical Engineer

Marietta, GA · On-site

$94K - $125K/yr

Apply engineering principles to existing and proposed processes working with various clients ... Industries may include foods, pharmaceutical, pulp and paper, chemical & other industries. Be ...

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Showing results 1-20

Pharmaceutical Engineer information

See Georgia salary details

$28

$32

$35

How much do pharmaceutical engineer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for pharmaceutical engineer in Georgia is $32.48, according to ZipRecruiter salary data. Most workers in this role earn between $30.87 and $34.09 per hour, depending on experience, location, and employer.

What does a pharmaceutical engineer do?

Pharmaceutical engineers design and manufacture pharmaceutical products. As a pharmaceutical engineer, the focus of your work may be on chemical research, manufacturing design, field testing, quality assurance, packaging and labeling, product delivery, or regulations compliance. Your job duties include collaborating with other engineers and manufacturing personnel, and ensuring all procedures follow Good Manufacturing Practice Regulations established by the Food and Drug Administration (FDA). You need extensive science experience, strong analytical and problem-solving skills, and the ability to work well with a team.

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

To thrive as a Pharmaceutical Engineer, you need a strong background in chemical or biomedical engineering, pharmaceutical sciences, and process development, typically supported by a relevant bachelor's or master's degree. Familiarity with Good Manufacturing Practice (GMP) regulations, process simulation software, and quality assurance systems is essential. Exceptional problem-solving, attention to detail, and teamwork skills help you excel in cross-functional environments. These skills ensure safe, efficient drug production and regulatory compliance, which are vital for patient safety and business success.

How do pharmaceutical engineers typically collaborate with cross-functional teams during drug development projects?

Pharmaceutical engineers work closely with scientists, quality assurance specialists, regulatory teams, and manufacturing staff throughout the drug development process. They play a key role in translating laboratory-scale processes into safe, efficient, and scalable manufacturing solutions. Effective communication and teamwork are crucial, as engineers must ensure that all technical, safety, and compliance requirements are met while balancing project timelines and budgets. This collaborative environment offers valuable opportunities to broaden your expertise and develop leadership skills, especially as you take on more responsibility in project management or process optimization roles.

What is the difference between Pharmaceutical Engineer vs Chemical Engineer?

AspectPharmaceutical EngineerChemical Engineer
CredentialsBachelor's in Pharmaceutical Engineering, Chemical Engineering, or related field; often requires industry-specific certificationsBachelor's in Chemical Engineering; professional engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, quality controlChemical plants, refineries, research labs
Industry UsagePrimarily in pharmaceutical and biotech industriesBroader industries including chemicals, energy, and materials
Job FocusDesigning and optimizing drug manufacturing processes, ensuring compliance with regulationsDesigning chemical processes, scaling up production, safety analysis

While both roles require a background in chemical processes, Pharmaceutical Engineers focus specifically on drug manufacturing and regulatory compliance within the pharmaceutical industry. Chemical Engineers have a broader scope, working across various chemical production sectors. The choice depends on your industry interest and specialization goals.

What cities in Georgia are hiring for Pharmaceutical Engineer jobs?

Cities in Georgia with the most Pharmaceutical Engineer job openings:

What are popular job titles related to Pharmaceutical Engineer jobs in GA?

For Pharmaceutical Engineer jobs in GA, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Engineer job openings in Georgia as of August 2026, with employment types broken down into 85% Full Time, 4% Part Time, 8% Contract, and 3% Nights. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $67,550 per year, or $32.5 per hour.

Pharmaceutical - Siemens Desigo / Insight Building Automation Engineer USA

MMR Consulting

Alpharetta, GA

Full-time

Posted 6 days ago


Job description

The work will require working out of client's facilities in Raileigh , North Carolina. Relocation support or travel expanses may be offered for qualified candidate.


MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.


MMRhasofficesinCanada,USA,andAsia.


Thisisanoutstandingopportunitytojoinourgrowingteam,wherethesuccessfulcandidatewillworkwithagroupofengineersandspecialistsinvolvedintheengineeringandprojectmanagementofequipment,systemsandfacilitiesforlifesciencesfacilities.ThisroleisbasedinSanDiego,California.Sometraveltootherclientsitesisexpected.

This role is for a Pharmaceutical - Siemens Desigo / Insight Building Automation Engineer USAtoworkonthedesign,projectexecutionandcommissioningofprocesssystemsinthebiopharmaceuticalindustry.Theidealcandidateshouldpossessleadershipskillstolead/mentorjuniorengineers,equipmentvendors,andcontractors.

Responsibilities

  • Providetechnicalguidanceintothedesign,projectmanagement,commissioningandstart-upofautomationsystems,forupgrades,renovationsandexpansionsofclientfacilitiesandprocesses.
  • SupportprojectexecutionfromFeasibilitythroughtoprojectcompletion/handover,includingallprojectstagessuchas:

Feasibility

ConceptDesign,BasicDesign,DetailedDesign

Procurement

Construction

ProjectMonitoring/Governance

Commissioning&Qualification

  • TheidealcandidatehasexperienceinBuildingAutomationSystems(BAS)suchasSiemensInsight,SiemensDesigoinbiopharmaceuticalindustry.
  • Prepare/perform/reviewelectricaldrawings,suchasPanelDrawings,wiringdiagrams,singlelinedrawings.
  • Performprogramming/configurationonBAS.
  • Reviewprogrammingofequipmentvendorsandotherautomationfirms
  • Performautomation/electricaltroubleshootingonelectricalpanelsandcontrolsystems
  • FacilitateworkeffortswithotherdisciplinessuchasProcessEngineering,Mechanical,Validation,andclient'sinternalstakeholders.
  • Prepare/reviewUserRequirementsSpecifications(URS),FunctionalRequirementsSpecifications(FRS),SDS,DDS,Valve&AlarmMatrices.
  • ProvideinputintoCommissioning(FAT,SAT)andQualificationProtocols(IQOQ),aswellassupportexecutionofCommissioning&Qualification.
  • Facilitateprojectmanagementtoolsthroughouttheexecutionofprojects,suchasprocurementtracking,vendormanagement,meetingminutes/actionlists,riskregisterlog,scheduleupdates,projectupdates.
  • Coordinatemeetingswithcross-functionaldepartments,todriveprojectprogress,facilitatedecisions,andprovideupdates.
  • Travelmaybeoccasionallyrequiredformeetingswithclients,equipmentfabricationvendorsorFactoryAcceptanceTesting(FATs).
  • Workmayrequireoccasionalsupportovershutdownsorextendedhours,specificallyduringinstallationandcommissioning/validationphases.
  • Client-management(maintainkeyClientrelationshipsinsupportofbusinessdevelopmentandpursuitofnewwork),projectscheduling/budgeting,coordinationofclientandMMRresourcesforeffectiveprojectdelivery,supportingbusinessdevelopment(providingtechnicalsupporttothesalesasrequiredforproposals/opportunities),presentingatindustryconferences/publishingpapersetc.
  • Asthispositionrequiresworkingonclientsites,youwillneedtocomplywiththeclient'ssafetyrulesincludingmandatoryvaccinationpoliciesforCOVID-19,whereapplicable
  • Visitconstructionandinstallationsites.
  • Supervisecontractorsduringcriticalinstallationsofprocessequipmentandassociatedutilities.
  • Otherdutiesasassignedbyclient,and/orMMR,basedonworkloadandprojectrequirements.

Qualifications

  • ExcellentwrittenandspokenEnglishisrequiredincludingthepreparationoftechnicaldocumentsinEnglish
  • KnowledgeofGMPrequirementsforworkinginpharma/biotechfacilities,withaBasicunderstandingofSOPs,Validation,ChangeControls.
  • KnowledgeofGAMPanddataintegrityrequirements
  • Engineeringdegree,preferablyinElectrical,Electromechanical,Controls,Chemical,MechanicalEngineeringorarelateddiscipline.
  • Yearsofexperience:

Minimum5+yearsofpharma(8+yearsispreferred)buildingautomationengineeringexperience,withatleast3years(5+yearsispreferred)ofbuildingcontrolsexperiencewithBAS.

  • KnowledgeofSiemensInsightorDesigo,includingreadingcodeandmakingsmallcodemodifications.
  • Abilitytoreadelectricaldrawings,andSiemensBASCode(InsightorDesigo).
  • Possessleadershipskills,andbeabletotakeinitiativetoleadprojects,involvingmultiplestakeholders,departments,andvaryingcomplexity.
  • Possessmentorshipskills,tocoachanddevelopjuniorandintermediateemployees.
  • BasicknowledgeofAutoCADisanasset.
  • Abilitytohandlemultipleprojectsandworkinafast-pacedenvironment.
  • Strongmulti-taskingskills
  • Abilitytolift50lbs.


As part of our recruitment process, we may use technology-assisted tools, including AI-enabled systems, to support application review and candidate evaluation. Hiring decisions are made with human oversight and consideration.


Equal Employment Opportunity and Reasonable Accommodations

MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.