Senior Associate Attorney – Insurance Defense (Hybrid | Georgia Bar Required)
Location: Georgia (Hybrid Work Schedule)
Job Type: Full-Time
Salary Range: $120,000 – $175,000 (DOE)
Our client, a well-established civil litigation firm, represents major insurance carriers in complex insurance defense, bodily injury, and liability matters. They are seeking a Senior Associate Attorney to play a key role in handling time-sensitive conditional demands and driving case strategy.
This is an excellent opportunity for an experienced litigation attorney who thrives in a fast-paced, deadline-driven environment and is looking for long-term growth.
Key ResponsibilitiesDraft and respond to time-limited conditional demands with precision and urgencyDraft, review, and manage legal documents including pleadings, motions, briefs, affidavits, and settlement agreementsConduct legal research and develop case strategy in collaboration with senior attorneysAnalyze liability, exposure, and risk to advise clients on case direction and resolutionCommunicate directly with clients, including explaining legal strategies to non-legal stakeholdersCollaborate with attorneys, paralegals, and staff to ensure efficient case managementMaintain accurate and organized case files and documentationManage deadlines across multiple matters and meet billable hour requirementsQualificationsActive Georgia Bar admission (required)5–7+ years of insurance defense or civil litigation experienceStrong background handling bodily injury, liability, or complex litigation casesExperience managing time-sensitive legal matters and deadlinesExcellent legal writing, analytical, and research skillsStrong communication skills with the ability to interface with clients and internal teamsHighly organized, self-motivated, and able to manage a high-volume caseloadPreferred ExperienceExperience responding to time-limited demand lettersBackground working with insurance carriers or defense firmsFamiliarity with case management systems and legal technology toolsCompensation & BenefitsCompetitive base salary: $120,000 – $175,000 (DOE)Hybrid work scheduleMedical, dental, and vision insuranceFirm-paid life insurance and long-term disability401(k) with profit sharingAdditional voluntary benefitsSupportive, team-oriented environment with opportunities for advancementApply TodayIf you're a Senior Associate Attorney with insurance defense experience looking to join a respected firm with a strong pipeline of work, we encourage you to apply.
Read LessJob Title: Quality Control Laboratory Chemist
Department: Quality Control
Reports To: Quality Control Manager
Employment Type: Full-Time | On-Site
Location: Gulfport, MS
Compensation: Median $60,000-$70,000/year
Our client is seeking an experienced Quality Control Laboratory Chemist to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a GMP-regulated laboratory environment. This position requires a strong background in chromatography and a proven track record of working within cGMP standards.
Please note that you must have experience beyond a university based laboratory setting to be considered for this position.
Key ResponsibilitiesPerform chemical analyses on raw materials, in-process products, finished products, and stability samples.Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.).
Prepare reagents and samples in compliance with SOPs and regulatory requirements.
Accurately document and report test results according to GMP guidelines.
Contribute to method development, validation, and transfer activities.
Troubleshoot and investigate testing or equipment-related issues.
Collaborate with QC team members and cross-functional departments.
Mentor and support junior chemists when needed.
Qualifications & Requirements3-5 years of direct hands-on experience in a GMP-regulated QC or manufacturing laboratory.Strong background in chromatography (HPLC, GC, UV/VIS, FTIR).
Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing.
Proficiency with Empower, Microsoft Office, and laboratory data systems.
Solid understanding of cGMP, quality systems, and regulatory compliance (change control, deviations, CAPAs).
Excellent attention to detail, communication, and organizational skills.
Ability to multitask and prioritize in a fast-paced environment.
Note: Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most.
Physical RequirementsMust be able to lift 50 lbs. or more daily.
Ability to stand, walk, or sit for 8+ hours per day.
Read LessJob Title: Quality Control Laboratory Chemist
Department: Quality Control
Reports To: Quality Control Manager
Employment Type: Full-Time | On-Site
Location: Gulfport, MS
Compensation: Median $23-$25/hour (commensurate with experience)
Our client is seeking an experienced Quality Control Laboratory Chemist to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a GMP-regulated laboratory environment. This position requires a strong background in chromatography and a proven track record of working within cGMP standards.
Please note that you must have experience beyond a university based laboratory setting to be considered for this position.
Key ResponsibilitiesPerform chemical analyses on raw materials, in-process products, finished products, and stability samples.Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.).
Prepare reagents and samples in compliance with SOPs and regulatory requirements.
Accurately document and report test results according to GMP guidelines.
Contribute to method development, validation, and transfer activities.
Troubleshoot and investigate testing or equipment-related issues.
Collaborate with QC team members and cross-functional departments.
Mentor and support junior chemists when needed.
Qualifications & Requirements3-5 years of direct hands-on experience in a GMP-regulated QC or manufacturing laboratory.Strong background in chromatography (HPLC, GC, UV/VIS, FTIR).
Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing.
Proficiency with Empower, Microsoft Office, and laboratory data systems.
Solid understanding of cGMP, quality systems, and regulatory compliance (change control, deviations, CAPAs).
Excellent attention to detail, communication, and organizational skills.
Ability to multitask and prioritize in a fast-paced environment.
Note: Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most.
Physical RequirementsMust be able to lift 50 lbs. or more daily.
Ability to stand, walk, or sit for 8+ hours per day.
Read Less