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Produce Quality Inspector Jobs in Raleigh, NC (NOW HIRING)

GRIFOLS, S.A.

Manager, Quality Audits

Clayton, NC · On-site

We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market ... inspections and supplier audits and issue reports. • Follow up on post audit action tracking ...

Millennium Print Group

Slitter Operator

Raleigh, NC · On-site

$17.25 - $20.75/hr

Operate slitter equipment to produce high-quality trading cards that meet production and quality ... Inspect product samples throughout the shift and document results * Communicate job status and ...

Millennium Print Group

Slitter Operator, Nights

Raleigh, NC · On-site

$17.25 - $20.75/hr

Operate slitter equipment to produce high-quality trading cards that meet production and quality ... Inspect product samples throughout the shift and document results * Communicate job status and ...

AtWork!

Industrial Batch Mixer (1st Shift)

Zebulon, NC · On-site

$18 - $20/hr

... produce alcohol beverages Observe equipment to troubleshoot possible malfunctions Report ... Quality Inspection experience in manufacturing Ability to follow detailed work instructions. Good ...

Millennium Print Group

Slitter Operator/ NIGHTS

Durham, NC · On-site

$17.25 - $20.50/hr

... produce high-quality card products Review production schedules and job specifications prior to production runs Set up jobs and make machine adjustments to support production efficiency Inspect ...

Adecco

Electrical Assembler

Knightdale, NC

$20/hr

... visual inspection. * Ability to read wire tables, line diagrams and ensure wire is properly ... Desire to produce quality products to be used in larger assemblies. * Ensures and double checks ...

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How much do produce quality inspector jobs pay per hour?

As of May 28, 2026, the average hourly pay for produce quality inspector in Raleigh, NC is $19.82, according to ZipRecruiter salary data. Most workers in this role earn between $15.67 and $22.45 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Produce Quality Inspector, and why are they important?

To thrive as a Produce Quality Inspector, you need expertise in food safety standards, quality control procedures, and experience with agricultural products, often supported by a background in food science or agriculture. Familiarity with inspection tools, data entry systems, and certifications like HACCP or USDA inspection credentials is frequently required. Attention to detail, strong observational skills, and effective communication are vital soft skills for accurately assessing product quality and collaborating with suppliers. These skills ensure that only safe, high-quality produce reaches consumers, protecting public health and reducing supply chain losses.

What are some common challenges faced by Produce Quality Inspectors, and how can they be addressed on the job?

Produce Quality Inspectors often face challenges such as managing varying quality standards among suppliers, working in fast-paced environments, and identifying subtle defects in produce. To address these issues, inspectors rely on clear communication with suppliers and team members, continuous training on updated quality standards, and the use of standardized checklists and tools. Staying organized and maintaining meticulous records also help ensure consistency and accuracy in inspections, which is crucial for food safety and customer satisfaction.

What does a Produce Quality Inspector do?

A Produce Quality Inspector is responsible for examining fruits, vegetables, and other produce to ensure they meet specific quality and safety standards. They look for signs of damage, spoilage, ripeness, and contamination, and may also check for correct labeling and packaging. Their work helps maintain food safety throughout the supply chain and ensures customers receive high-quality produce. Inspectors often work in warehouses, distribution centers, or at points of import and export.

What is the difference between Produce Quality Inspector vs Food Safety Inspector?

AspectProduce Quality InspectorFood Safety Inspector
CertificationsQuality assurance certifications, HACCP knowledgeFood safety certifications, HACCP, ServSafe
Work EnvironmentFarms, processing plants, warehousesRegulatory agencies, inspection sites, food facilities
Industry UsageProduce, agriculture, food processingFood manufacturing, regulatory compliance

The Produce Quality Inspector focuses on assessing the quality and freshness of produce, ensuring it meets standards before distribution. In contrast, the Food Safety Inspector evaluates overall food safety compliance across various food facilities. While both roles require knowledge of HACCP and food safety protocols, their work environments and specific responsibilities differ, with Produce Quality Inspectors concentrating on produce quality and Food Safety Inspectors on regulatory compliance across the food industry.

What are popular job titles related to Produce Quality Inspector jobs in Raleigh, NC? For Produce Quality Inspector jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Produce Quality Inspector jobs in Raleigh, NC look for? The top searched job categories for Produce Quality Inspector jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Produce Quality Inspector jobs? Cities near Raleigh, NC with the most Produce Quality Inspector job openings:
Produce Quality Inspector jobs near you

Sr. Quality Systems Specialist, Quality Operational Readiness (QOR)

GRIFOLS, S.A.

Clayton, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Position Summary:
The Global Quality Operational Readiness (QOR) Sr. Quality Systems Specialist supports the implementation and operational readiness of Quality functions at new Biopharma manufacturing facilities (as well as new processes/faciltities at existing sites) across the EU, US, Canada, and other global locations. This role is instrumental in ensuring new sites meet global regulatory requirements and internal quality standards from the inception. The Global Quality QOR Sr. Quality Systems Specialist will work in the framework of cross-functional quality teams, including Subject Matter Experts (SMEs), and collaborate closely with Grifols BioPharma site's Engineering, Manufacturing, Regulatory Affairs, IT, and Global Quality to establish robust quality systems and processes aligned with cGMP and global health authority expectations. May serve as manager delegate with demonstrated experience, as applicable.
Primary Responsibilities:
  • Facilitate the transfer of knowledge and best practices from other established Grifols sites (Technology Transfer process). Focus will be on identifying and implementing best practices that are cGMP compliant, inspection-tested and successful, as well as efficient. These best practices will be contemporary with health authorities/regulatory agencies expectations.
  • Collaborate with cross-functional teams (Engineering, Manufacturing, Regulatory Affairs, IT) to ensure quality is embedded in all aspects of site design and operations for new start up process.
  • Monitor project timelines, quality milestones, and risk mitigation plans for site readiness. Keep results (KPIs) visible to all stakeholders and to senior management on routine basis.
  • Ensure readiness for regulatory inspections through comprehensive planning, mock audits, and gap assessments. Conduct practice sessions with key site personnel to have successful interactions with regualtory inspectors.
  • Assist new start up site with review of validation master plans, sampling plans, master data setup, site master file development, product and raw material specifications, etc...
  • Use expertise and sound judgement to make recommendations to site Quality and Global Quality regarding improvement opportunities.
  • Assist BioPharma sites with recommendations for problem solving, mitigation of identified quality risks, and improvement of processes. Use quality risk-based approaches.
  • Monitor needed timelines and a sense of urgency with site Quality contacts so that the overall project milestones are not adversely impacted by quality support. In all cases, ensure competent quality oversight is established in the new site processes.
  • Carry out visits to production plants to ensure compliance with regulations and quality standards. Perform walkthroughs in manufacturing, warehouse, other GMP areas to identify continuous improvement opportunities and partner with site management to get the improvements in place.
  • Proactively identify quality related solutions and robust quality systems (as will be needed for day to day effective operations or during review by external regulators). Emphasze proactive problem-solving rather than reactionary responses. Ensure quality systems are mapped accordingly.

Additional Responsibilities:
This position will work with individuals and teams of SMEs from within QOR and at the BioPharma sites to drive and monitor continous improvement and operational preparedness activities.
Knowledge, Skills, and Abilities:
  • Analytical Thinking: Capability to analyze data and metrics to inform decision-making and identify areas for improvement
  • Communication: Proven, successful communication skills to effectively convey quality standards and expectations to diverse stakeholders
  • Risk Management: Proficiency in identifying, assessing, and mitigating risks associated with product quality and compliance
  • Problem-Solving: Ability to quickly identify quality issues and recommend effective solutions to maintain quality standards
  • Regulatory Knowledge Management: Demonstrated understanding of regulatory requirements (U.S. FDA, EMA, Health Canada, etc...)
  • Collaboration: Ability to work collaboratively with other departments and external partners to ensure quality across the entire process
  • Project Management: Skills to monitor multiple quality initiatives and projects simultaneously, ensuring timely and successful completion. Reporting of progress on frequent basis to management.

Requirements:
PhD in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred: science, biotechnology/technology, engineering, math, or computer science) with a minimum of 4 years relevant experience. MS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred: science, biotechnology/technology, engineering, math, or computer science) with a minimum of 6 years relevant experience. BS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred: science, biotechnology/technology, engineering, math, or computer science) with a minimum of 7 years relevant experience OR an equivilant combination of education and experience.
Occupational Demands:
There is a requirement for travel for this position. It is expected to have 15% to 50% travel to the other Biopharma sites in scope of support by Qualtiy Operational Readiness. Some of this travel will be international travel.
The position is eligible to participate in the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: This position supports and establishes Quality functions at new Biopharma manufacturing facilities (as well as new processes/faciltities at existing sites) in North America, Europe, and other global locations.
Learn more about Grifols

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