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Gdp Jobs (NOW HIRING)

Aequor

Note: Hybrid - 3 days Onsite (Tues, Wed, Thurs) and 2 days WFH Standard hoursTop 3 Must Have Skill Sets: • Bachelor's degree or equivalent in Life Sciences + 2 years' experience in GMP / GDP ...

Posted today

Brooksource

Quality Technician

Minneapolis, MN · On-site

$52K - $63K/yr

Review test/ inspection data and ensure data adheres to Data Integrity requirements, including Good Documentation Practices (GDP) * Perform basic electronic data entry, calculations, and data ...

Aptyx

Production Lead

Taunton, MA · On-site

$58K - $63K/yr

Provide GDP and packaging-specific training for staff, ensuring team members are certified and competent in relevant procedures; deliver ongoing coaching and refresher sessions as needed.Assist in ...

Aptyx

Production Lead

Taunton, MA · On-site

$58K - $63K/yr

Provide GDP and packaging-specific training for staff, ensuring team members are certified and competent in relevant procedures; deliver ongoing coaching and refresher sessions as needed. * Assist in ...

Aptyx

Production Lead

Taunton, MA

$19.25 - $26.50/hr

Provide GDP and packaging-specific training for staff, ensuring team members are certified and competent in relevant procedures; deliver ongoing coaching and refresher sessions as needed. * Assist in ...

Aptyx

$19.25 - $26.50/hr

Provide GDP and packaging-specific training for staff, ensuring team members are certified and competent in relevant procedures; deliver ongoing coaching and refresher sessions as needed. Assist in ...

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Showing results 21-40

All JobsGdp Jobs

GDP information

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$17

$32

$52

How much do gdp jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for gdp in the United States is $32.71, according to ZipRecruiter salary data. Most workers in this role earn between $25.96 and $38.46 per hour, depending on experience, location, and employer.

What is a GDP?

GDP jobs are roles that involve collecting, analyzing, and reporting data related to Gross Domestic Product (GDP). These professionals may work for government agencies, statistical organizations, or research institutions to help measure a country's economic performance. Common tasks include compiling economic data, performing statistical analysis, and preparing reports that inform policymakers and the public. GDP jobs often require strong analytical skills and a background in economics, statistics, or a related field.

What are the key skills and qualifications needed to thrive as a GDP (Good Distribution Practice) Responsible Person, and why are they important?

To thrive as a GDP Responsible Person, you need a strong background in pharmaceutical regulations, supply chain management, and compliance, often supported by a relevant degree and industry experience. Familiarity with quality management systems, regulatory databases, and audit processes is typically required, along with certifications in GDP or related areas. Attention to detail, integrity, and effective communication are vital soft skills for ensuring compliance and fostering collaboration across departments. These skills and qualifications are crucial for maintaining product quality, regulatory adherence, and patient safety throughout the distribution process.

What are some typical responsibilities of an economic analyst working with GDP data within a financial institution?

Economic analysts focusing on GDP data are typically responsible for collecting, analyzing, and interpreting national and international economic indicators to forecast economic trends and advise internal teams or clients. They often prepare detailed reports, present findings to stakeholders, and collaborate closely with economists, policy advisors, and market strategists. Analysts may also be tasked with monitoring policy changes, conducting sector-specific research, and using statistical software to model economic scenarios. This role requires strong analytical skills, attention to detail, and the ability to communicate complex economic concepts clearly.

What is the difference between Gdp vs Data Analyst?

AspectGdpData Analyst
Required CredentialsBachelor's degree often in economics, finance, or related fieldsBachelor's degree in statistics, mathematics, or related fields
Work EnvironmentFinancial institutions, government agencies, consulting firmsCorporate, finance, healthcare, marketing sectors
Industry UsageEconomics, finance, policy analysisBusiness, marketing, healthcare, technology

Gdp (Gross Domestic Product) measures the total economic output of a country, while a Data Analyst interprets data to inform business decisions. Both roles require analytical skills, but Gdp is a macroeconomic indicator, whereas Data Analysts focus on specific datasets within organizations.

More about GDP jobs

What states have the most Gdp jobs?

States with the most job openings for Gdp jobs include:

What job categories do people searching Gdp jobs look for?

The top searched job categories for Gdp jobs are:

GDP jobs near you
Infographic showing various Gdp job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 16% Part Time, 5% Contract, and 2% Nights. Highlights an 75% Physical, 1% Hybrid, and 24% Remote job distribution, with an average salary of $68,027 per year, or $32.7 per hour.

Quality Assurance Specialist - Clinical Trial Supply

JUPITER RESEARCH SERVICES INC

Edison, NJ

$40K - $55K/yr

Full-time

Re-posted 16 days ago

Job description

Benefits/Perks
  • Highly enriched & healthy work environment
  • Excellent growth opportunities
  • Competitive Pay
  • Career Advancement
Job Summary
We are seeking an experienced Quality Assurance Specialist to join our team. In this role, you will be responsible for overseeing the quality of goods and services our company provides. You will perform routine inspections, implement quality assurance policies and procedures, and identify any workflow issues. The ideal candidate is an excellent verbal and written communicator with strong attention to detail. 

Position Summary

The Quality Assurance Specialist – Clinical Trial Supply plays a critical role in ensuring the quality, safety, integrity, and compliance of clinical trial materials throughout their lifecycle—from receipt and storage to packaging, labeling, distribution, and returns.
This role supports GxP operations, oversees Quality System activities, and collaborates cross-functionally with Operations, Warehouse, Packaging, Project Management, and external suppliers/CROs to maintain compliance with FDA, EU-GMP, GDP, ICH-GCP, DSCSA, and internal JRS standards.
The QA Specialist ensures that all products and processes meet regulatory and customer expectations while supporting JRS’s mission to deliver reliable, resilient, and high-quality clinical supply solutions worldwide.
Key Responsibilities

1. Quality Systems & Compliance

  • Ensure compliance with GMP, GDP, GCP, ICH, FDA, EMA, MHRA, TGA, CDSCO and JRS internal SOPs.
  • Review, approve, and maintain controlled documents including SOPs, Work Instructions, Forms, Batch Records, Labeling Specs, and Packaging Records.
  • Support implementation and continuous improvement of Quality Management Systems (QMS) including Deviation Management, CAPA, Change Control, Training, and Document Control.
  • Participate in internal audits, customer audits, vendor qualifications, and regulatory inspections.
2. Clinical Supply Chain Quality Oversight

  • Perform QA review and approval of:
    • Incoming clinical supplies (comparator drugs, IMPs, ancillary supplies)
    • Packaging and labeling activities
    • Storage and temperature monitoring records
    • Distribution documentation including shipping records, AWBs, and temperature logger data
  • Verify completion and accuracy of Line Clearance, Batch Packaging Records (BPR), and Label Control Logs.
  • Review and approve EPCIS/DSCSA traceability files, CoA/CoC, pedigrees, and other regulatory documentation.
3. Investigations & Deviation Management

  • Lead or support investigations for:
    • Temperature excursions
    • Packaging or labeling discrepancies
    • Shipment issues
    • Supplier or customer complaints
  • Perform root cause analysis (RCA), risk evaluation, and implement effective CAPAs.
4. Vendor & Customer Quality Support

  • Support supplier qualification by reviewing:
    • GMP/GDP licenses
    • ISO certifications
    • Quality Agreements (QTA)
    • Questionnaires and risk assessments
  • Collaborate with customers to ensure project-specific quality requirements are met.
5. Documentation & Regulatory Support

  • Ensure accurate completion of QA documentation related to:
    • Clinical supply release
    • Temperature-controlled shipping
    • Storage of controlled and non-controlled materials
    • Destruction, return, and reconciliation
  • Maintain updated Quality and Technical Agreements (QTA) with clients and suppliers.
6. Training & Continuous Improvement

  • Deliver and maintain training programs for QA and Operations teams on:
    • GDP/GMP compliance
    • SOP revisions
    • Packaging and labeling quality requirements
    • Temperature control best practices
  • Participate in continuous improvement initiatives to enhance operational efficiency and compliance.
Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, or related field.
  • 2–5 years of experience in Quality Assurance within Clinical Trial Supply, Pharmaceutical, Biotech, CRO, CDMO, or GMP/GDP warehouse environment.
  • Strong understanding of GMP, GDP, GCP, DSCSA/EPCIS, ICH guidelines, and clinical supply chain processes.
  • Experience with deviations, CAPA, change control, labeling review, packaging operations, and QA release.
Preferred Qualifications

  • Experience working with temperature-controlled logistics (2–8°C, -20°C, CRT).
  • Knowledge of comparator sourcing workflows and global distribution practices.
  • Familiarity with Quality Agreements, Supplier Qualification, and Vendor Audits.
  • Experience with Power BI, SharePoint QMS, and ERP/WMS systems.
  • Certification in GMP/GDP/GCP (optional but advantageous).
Core Competencies

  • Strong attention to detail and documentation accuracy.
  • Excellent communication and problem-solving skills.
  • Ability to work cross-functionally and manage multiple priorities.
  • Proactive, organized, and committed to quality and compliance.
  • Ability to make decisions based on risk, data analysis, and regulatory expectations.
Why Join Jupiter Research Services?

  • Work in a rapidly growing organization focused on resilient clinical supply chain solutions.
  • Gain exposure to global clinical trials, high-impact projects, and innovative supply models.
  • Contribute to a compliance-driven organization with strong customer and patient-centric values.
  • Opportunities for growth in Quality, Operations, Regulatory, and Project Management.