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3Rd Shift Pharmaceutical Coding Jobs (NOW HIRING)

Ardena

3rd Shift Supervisor

Somerset, NJ · On-site

Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex ... Ardena is hiring a 3rd Shift Supervisor; hours 11:00pm- 7:30am , to join the Manufacturing ...

Sarahbush

$109K - $169K/yr

Pharmacist NS (3rd Shift) The Pharmacist is responsible for the delivery of ... pharmaceutical care to patients, including processing of medication and IV orders and the ...

J Edward Staffing LLC

Pharmacist (Allied)

Methuen, MA · On-site

$61 - $73.25/hr

Third shift pharmacist 9P-7A, Wed-Tues 7 nights on, 7 nights off. The pharmacist is responsible for ensuring safe, effective, and efficient medication use within the hospital setting. This role ...

Varite

Pharmacist (Allied)

Methuen, MA · On-site

$95 - $98/hr

Third shift pharmacist 9P-7A, Wed-Tues 7 nights on, 7 nights off. The Pharmacist is responsible for ensuring safe, effective, and efficient medication use within the hospital setting. This role ...

ExactCare Pharmacy

PRN Pharmacist (Third Shift)

Cleveland, OH · On-site

$56.50 - $67.75/hr

PRN Pharmacist (Third Shift) page is loaded## PRN Pharmacist (Third Shift)locations: OH\_Clevelandtime type: Part timeposted on: Posted 2 Days Agojob requisition id: R-108547**AnewHealth is one of ...

Synchrony Pharmacy Columbus

Customer Care Rep

Hilliard, OH · On-site

$15.25 - $20.50/hr

Responsibilities This position will work closely with the 3rd shift pharmacist following up on customer phone calls after hours and must possess effective and professional communication skills.

Synchrony Pharmacy

Customer Care Rep

Hilliard, OH · On-site

$15.25 - $20.50/hr

Responsibilities This position will work closely with the 3rd shift pharmacist following up on customer phone calls after hours and must possess effective and professional communication skills.

Synchrony Pharmacy Columbus

Customer Care Rep

Hilliard, OH · On-site

$15.25 - $20.50/hr

Responsibilities This position will work closely with the 3rd shift pharmacist following up on customer phone calls after hours and must possess effective and professional communication skills.

Trilogy Health Services

Customer Care Rep

Hilliard, OH · On-site

$15.25 - $20.50/hr

This position will work closely with the 3rd shift pharmacist following up on customer phone calls after hours and must possess effective and professional communication skills. Background in ...

Manpower

3rd Shift Maintenance Mechanic

Milwaukee, WI · On-site

$71K - $85K/yr

As a 3rd shift Mechanic, you will be part of the Maintenance Department supporting manufacturing ... Knowledge of electrical theory, codes, and safety standards (e.g., NEC, arc flash). * Proficiency ...

Stabilus

Be Seen First

Maintenance Technician 3rd Shift

Gastonia, NC · On-site

$31 - $33/hr

Follow all applicable safety, environmental, and electrical codes Qualifications * Associate ... shift premium for 3rd shift * Overtime opportunities * Hands-on experience with cutting-edge ...

Actalent

Aseptic Technician 3rd Shift

Fairfield, NJ · On-site

$23 - $24/hr

Aseptic Technician 3rd Shift This role focuses on supporting aseptic operations in ISO 6 and 7 ... Industry experience of approximately 12 years in pharmaceutical, biotech, medical device, or ...

Actalent

Aseptic Technician 3rd Shift

Fairfield, NJ · On-site

$23 - $24/hr

Aseptic Technician 3rd Shift This role focuses on supporting aseptic operations in ISO 6 and 7 ... Industry experience of approximately 12 years in pharmaceutical, biotech, medical device, or ...

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3Rd Shift Pharmaceutical Coding information

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$13

$28

$41

How much do 3rd shift pharmaceutical coding jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for 3rd shift pharmaceutical coding in the United States is $28.13, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $32.69 per hour, depending on experience, location, and employer.

What is 3rd shift pharmaceutical coding?

3rd shift pharmaceutical coding jobs involve assigning standardized codes to medications and pharmaceutical processes during overnight or late-night hours, typically between 11 p.m. and 7 a.m. Professionals in these roles work in pharmacies, hospitals, or pharmaceutical companies to ensure accurate documentation and billing for medications dispensed or processed. The 3rd shift is essential for 24-hour facilities, helping maintain up-to-date records and compliance with healthcare regulations. Workers in this shift often benefit from shift differentials and quieter work environments, but must adjust to a nocturnal schedule.

What are the key skills and qualifications needed to thrive as a 3rd shift pharmaceutical coding specialist?

To excel as a 3rd Shift Pharmaceutical Coding Specialist, you need a strong understanding of pharmaceutical terminology, coding systems (such as NDC and HCPCS), and attention to detail, typically supported by a background in pharmacy tech or medical coding. Familiarity with pharmacy management software, electronic health records (EHRs), and barcode scanning systems is often required, along with certification such as CPhT or CPC being advantageous. Strong analytical thinking, self-motivation, and effective communication are valuable soft skills for maintaining accuracy and working independently during night shifts. These competencies ensure precise medication data entry, regulatory compliance, and smooth pharmacy operations during off-hours.

What are some common challenges faced by 3rd shift pharmaceutical coding professionals, and how can they be managed?

Working the 3rd shift as a pharmaceutical coder often involves adapting to overnight hours, which can affect work-life balance and alertness. Additionally, accurate and timely coding is essential to ensure compliance and prevent billing delays, even during less supervised hours. To manage these challenges, it's helpful to establish a consistent sleep schedule, utilize effective time-management techniques, and communicate proactively with day-shift teams to ensure smooth handoffs and collaboration.

What is the difference between 3Rd Shift Pharmaceutical Coding vs 3Rd Shift Medical Billing Specialist?

Aspect3Rd Shift Pharmaceutical Coding3Rd Shift Medical Billing Specialist
CredentialsCertification in coding (e.g., CPC, CCS)Certification in billing and coding (e.g., CPC, CBC)
Work EnvironmentPharmaceutical companies, hospitals, healthcare facilitiesMedical offices, hospitals, billing companies
Industry UsageHealthcare and pharmaceutical industryHealthcare providers and insurance companies
Job FocusAssigning codes to pharmaceutical procedures and medicationsProcessing insurance claims and patient billing

While both roles involve coding and require similar certifications, 3Rd Shift Pharmaceutical Coding focuses on assigning codes to medications and pharmaceutical procedures within healthcare and pharmaceutical settings. In contrast, 3Rd Shift Medical Billing Specialists handle insurance claims and patient billing processes. Both roles operate during the third shift and serve the healthcare industry, but their specific responsibilities and focus areas differ.

What cities are hiring for 3Rd Shift Pharmaceutical Coding jobs?

Cities with the most 3Rd Shift Pharmaceutical Coding job openings:

What are the most commonly searched types of Pharmaceutical Coding jobs?

The most popular types of Pharmaceutical Coding jobs are:

What states have the most 3Rd Shift Pharmaceutical Coding jobs?

States with the most job openings for 3Rd Shift Pharmaceutical Coding jobs include:

What other helpful pages are available for 3Rd Shift Pharmaceutical Coding?

Other pages related to 3Rd Shift Pharmaceutical Coding:

3Rd Shift Pharmaceutical Coding jobs near you
Infographic showing various 3Rd Shift Pharmaceutical Coding job openings in the United States as of July 2026, with employment types broken down into 79% Full Time, 15% Part Time, 1% Temporary, 3% Contract, and 2% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $58,510 per year, or $28.1 per hour.

3rd Shift Supervisor

Somerset, NJ • On-site

Ardena
See more jobs at Ardenaexternal

Full-time

Medical, PTO

Re-posted 2 days ago

Job description

About Ardena
Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market.
The Ardena Group operates from five sites across Europe and the United States, employing more than 750 professionals. Ardena European sites are located in Oss and Assen (the Netherlands), Ghent (Belgium), and Pamplona (Spain). Ardena US facility is based in Somerset, New Jersey.
Ardena provides integrated services spanning drug substance development, drug product formulation, GMP manufacturing, bioanalytical services, clinical logistics, fill and finish, and CMC regulatory support.
Ardena is hiring a 3rd Shift Supervisor; hours 11:00pm- 7:30am, to join the Manufacturing/ Operations team at our Somerset, NJ site. This role supports pharmaceutical development and manufacturing activities within a GMP-regulated environment.
Role Description
As a 3rd Shift Supervisor at Ardena, you will contribute to pharmaceutical development projects by performing scientific, technical, or operational activities within the Operations. You will work in a regulated pharmaceutical environment, ensuring that all work meets GMP, GxP, and applicable ISO standards.
You will collaborate with cross-functional teams including Quality Assurance, Regulatory Affairs, Project Management, Production, and other departments across Ardena's European and US sites.
Summary
The Shift Supervisor is responsible for leading, training, and overseeing production personnel in a 24/5 pharmaceutical manufacturing environment. This role ensures safe, compliant, and efficient commercial and clinical manufacturing and packaging operations, including controlled substances (Schedules II-V). Responsibilities include staffing, quality oversight, production performance, material accountability, batch documentation, and continuous improvement initiatives to improve productivity and operational excellence.
Key Responsibilities
  • Supervise daily manufacturing and packaging operations in compliance with cGMP, FDA, DEA, OSHA, and company requirements.
  • Lead, coach, and develop production staff to ensure safe, compliant, and productive operations across shifts.
  • Coordinate staffing, employee training, cross-training, performance management, scheduling, time-card and time-off approvals.
  • Troubleshoot manufacturing and packaging equipment issues and support operational problem solving.
  • Ensure accurate completion and review of batch records, equipment logs, material reconciliation, label verification, and production documentation.
  • Verify production order consumption and batch closure activities within ERP systems.
  • Investigate production deviations, out-of-specification events, and customer complaints using the QMS.
  • Support continuous improvement initiatives through process enhancements, corrective actions, and quality system improvements.
  • Maintain compliance with PPE requirements, safety procedures, and workplace regulations.
  • Collaborate with Quality, R&D, Project Management, Warehouse, and other cross-functional teams to support clinical and commercial programs.
  • Oversee manufacturing operations including blending, milling, sifting, encapsulation, compression, coating, fluid bed processing, hot melt extrusion, and related unit operations.
  • Perform inventory transactions, staging activities, reconciliation, and label generation within ERP systems.
  • Perform other duties as assigned.

Required Qualifications:
Bachelor's Degree in Engineering, Chemistry, Mathematics, Physics, or related scientific discipline with:
  • 1+ years of experience in pharmaceutical, food, or other GMP-regulated manufacturing environments.
  • Previous project leadership or team leadership experience required.
  • Supervisory experience preferred.

OR
Associate Degree or equivalent experience with:
  • 4+ years of experience in pharmaceutical, food, or other GMP-regulated manufacturing environments.
  • 2+ years of leadership experience within a regulated manufacturing environment.

Knowledge & Skills
  • Working knowledge of FDA cGMP requirements and DEA regulations.
  • Strong leadership, communication, coaching, and team development skills.
  • Experience with pharmaceutical manufacturing and packaging processes and equipment.
  • Ability to review and complete GMP documentation accurately, including batch records and logbooks.
  • Knowledge of quality systems, deviation investigations, document control, and compliance requirements.
  • Experience with ERP and QMS platforms (e.g., Business Central, MasterControl) preferred.
  • Proficient in Microsoft Office applications.
  • Strong organizational, troubleshooting, and problem-solving capabilities.
  • Demonstrated ability to drive productivity improvements and reduce operational downtime.

Physical & Work Environment
This position is primarily based on the production floor with routine office work. The role requires standing, walking, and occasional lifting of up to 50 pounds. The environment is fast-paced and deadline-driven, requiring strong attention to detail, communication, and the ability to manage multiple priorities while maintaining compliance and operational excellence.
What Ardena Offers
Ardena is a science-driven and people-focused employer. Working at Ardena means contributing to pharmaceutical projects that support the availability, safety, and quality of medicines for patients worldwide.
Ardena offers an international working environment where employees are encouraged to develop their expertise, take ownership, and grow their careers across functions and locations.
Benefits and perks at Ardena include:
• Competitive salary and tailored benefits package (adjusted per role and location)
• Flexible working arrangements and paid annual leave (where applicable, depending on role and site)
• International and collaborative work environment across European and US sites
• Access to professional development and training programs
• Meaningful work on pharmaceutical development projects that advance patient health
• A values-driven culture guided by Ardena's CARE principles: Communicative, Accountable, Reliable, and Excellent
Salary Range: $90,000 - $100,000 BOE
How to Apply
Ready to advance your career in pharmaceutical development? Apply now through the Ardena Careers website at careers.ardena.com.
Department General Operations Locations Somerset (New Jersey, US)

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