Top 377 Critical facilities Jobs in Clayton, Nc

Manufacturing QA Specialist
Guerbet —Raleigh, NC
- Full-time
- Mid-level
- 3 years
- Warehouse
Facilities Engineer 3
Caterpillar —Clayton, NC
- $97,530 - $146,290 a year
- Full-time
- Engineering
- Pass drug screening
- Office
- Health savings account
- Paid holidays
1d
Production Operator (Collection, Packaging, Inspection) *ALL SHIFTS
Tekni-Plex —Clayton, NC
- $22 an hour
- Overtime
- High school diploma or GED
- Ability to lift 50 pounds
- Ability to stand for extended periods
- Health savings account
- AD&D insurance
Quick Apply
Director, Continuous Improvement
Eaton —Raleigh, NC
- $182,000 - $266,000 a year
- Hybrid work
- Background check
- Master's degree
- Bachelor's degree
- Retirement plan
Manufacturing Engineer
Siemens —Wendell, NC
- $74,970 - $128,520 a year
- Full-time
- Data analysis skills
- Mid-level
- Analysis skills
- Relocation assistance
Operations Supervisor
Kellanova —Cary, NC
- $76,160 - $99,960 a year
- Evenings as needed
- Mid-level
- High school diploma or GED
- Supervising experience
- AD&D insurance
- Disability insurance
Quality Assurance Area Specialist II (QA for FP)
Novo Nordisk —Clayton, NC
- Computer literacy
- Mid-level
- High school diploma or GED
- Paid holidays
- Disability insurance
1d
Production Supervisor - 1st Shift
Siemens —Wendell, NC
- $61,547 - $105,509 a year
- Full-time
- Mid-level
- 3 years
- High school diploma or GED
- Relocation assistance
Sr Associate Mfg I- Investigations
Amgen —Holly Springs, NC
- $86,048.05 - $116,417.95 a year
- Engineering
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
8d
Specialist Manufacturing Investigations
Amgen —Holly Springs, NC
- $107,545.40 - $145,502.60 a year
- Doctoral degree
- 5 years
- Engineering
- Disability insurance
- Health insurance
Associate Manufacturing - Bulk Drug Substance Downstream - Days
Amgen —Holly Springs, NC
- $70,985.20 - $96,038.80 a year
- 12 hour shift
- High school diploma or GED
- In-person
- Associate's degree
- Disability insurance
- Health insurance
Quality Assurance Area Specialist III (QA for QC)
Novo Nordisk —Clayton, NC
- High school diploma or GED
- Analysis skills
- Bachelor's degree
- Paid holidays
- Disability insurance
Network Services Engineer - Hybrid 60% Remote
Wake County Government —Raleigh, NC
- $77,676 - $139,818 a year
- Monday to Friday
- Hybrid work
- Computer science
- Computer Science
- Mid-level
Production Supervisor - 2nd Shift
Siemens —Wendell, NC
- $61,547 - $105,509 a year
- Full-time
- 3 years
- High school diploma or GED
- Analysis skills
- Relocation assistance
Associate Project Manager
ABB Inc. —Cary, NC
- $83,300 - $133,280 a year
- Full-time
- Remote
- Mid-level
- Travel
- US work authorization
- Health savings account
- AD&D insurance
Quick Apply
7d
Process Engineer I - Printed Packaging Material
Novo Nordisk —Clayton, NC
- Engineering
- Organizational skills
- Experience equivalent to degree accepted
- Paid holidays
- Disability insurance
7d
Facilities Engineer II - Clean Utilities - PS AM
Novo Nordisk —Clayton, NC
- CAD
- 5 years
- Computer literacy
- Paid holidays
- Disability insurance
Facilities Manager
US AMR-Jones Lang LaSalle Americas, Inc. —Raleigh, NC
- $105,000 - $115,000 a year
- Online Application
- Background check
- Travel
- US work authorization
- Paid parental leave
- Paid holidays
Quick Apply
Manufacturing Associate II
Sumitomo Pharma America, Inc. —Morrisville, NC
- $61,500 - $76,900 a year
- Weekends as needed
- Pass drug screening
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
9d
Supervisor, Production
Indivior —Raleigh, NC
- $88,000 - $100,000 a year
- Full-time
- 5 years
- Computer literacy
- Basic math
- Profit sharing
- Employee stock purchase plan
7d

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Manufacturing QA Specialist

Guerbet -
Raleigh, NC

Apply Now

Job Details

Full-time

Qualifications

Defect resolution root cause analysis
Preventive action implementation
Production deviation management
Quality control preventive actions
Corrective and preventive actions (CAPA)
Internal investigations
Manufacturing facility experience
Pharmaceutical company experience
Issue tracking
Quality assurance experience within pharmaceutical industry
Quality control experience within pharmaceutical industry
Productivity software
Visual inspection for quality control
Failure analysis

Full Job Description

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 100 years, we continuously innovate to improve the diagnosis, prognosis and quality of life of patients.

Customer Centricity, Cooperation, Audacity, Focus, and Responsibility are the values that we share and practice on a daily basis.

Working at Guerbet is not only being part of a multicultural team with nearly 3,000 people across more than 20 countries, but it is above all about playing a unique role in the future of medical imaging.

WHAT WE ARE LOOKING FOR

The Manufacturing Quality Assurance Specialist will operate in full compliance with applicable hygiene, safety, quality and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for. The Manufacturing Quality Assurance Specialist provides on-floor quality oversight across cGMP manufacturing operations, including formulation, filling, sterilization, packaging, and warehouse activities. The role ensures compliance with site SOPs and regulatory requirements through real time monitoring, review of critical process documentation, and verification of product and process controls. The position also supports sample inspections, responds to atypical quality events and nonconformance, facilitates containment and issue escalation, and partners with operations to ensure timely sampling, effective defect management, and continuous adherence to quality standards.

YOUR ROLE

Monitors compliance to meet or exceed site SOPs/cGMPs during production and warehouse operations.
Supports required QA inspections, i.e. Sample defect detection.
Ability to participate in internal audits, as requested.
Provides primary daily support to the production and warehouse area, up to and including tasks such as packaging line clearance verification, material segregation/containment, low product fill response, rework reconciliations/accountabilities, and documentation real time review.
Primary QA event response personnel that will respond to exceptions within the operations/packaging areas, having functions of initial exception impact assessment, product containment, bracketing, initial scope identification, and direction of immediate actions to take prior to resuming processing.
Assists personnel in the generation of operations/packaging area related exceptions.
Supports minor exceptions and phase II manufacturing investigations.
Attends daily operations staff communication meetings.
Team member of Facilities meetings regarding operations Preventive Maintenance/Calibration/Work Order status and scheduling.
Team members during area shutdown or maintenance projects as needed.
Assisting in punch list generation & verification, as well as area inspections pre/post activity.
Perform weekly walkthroughs of the operations/packaging area and communicate any observations to associated area management.
Ability to pass visual acuity exam for production and identification of quality product purposes.
Ability to support the batch release functions on an as needed basis.
Supports site and departmental initiatives.

YOUR BACKGROUND

Required Qualifications

Bachelor’s degree in Life Sciences, Engineering, or a related technical discipline (e.g., Biology, Chemistry, Microbiology, Pharmaceutical Sciences) required.
3-6 years of experience in pharmaceutical manufacturing, quality assurance, or aseptic operations required.
Hands-on experience providing QA oversight on the manufacturing floor, including formulation, filling, sterilization, packaging, or warehouse GMP operations required.
Prior experience performing or verifying line clearances, room clearances, and/or batch record review required.
Familiarity with deviation management, root cause analysis, and execution of corrective and preventative actions (CAPA) required.
Skilled competency with computers, MS Office software required

Preferred Qualifications

Experience observing and evaluating aseptic behaviors, gowning qualification, environmental controls, and contamination control practices preferred.
ASQ inspection certification preferred.
Experience working with ISO, FDA, or EU Annex-1 regulated environments preferred.
Experience with pharmaceutical CAPA systems (e.g., Trackwise, Metric Stream, etc.)

Apply Now

Refine Your Search

critical facilities jobs in clayton, nc

Manufacturing QA Specialist

Facilities Engineer 3

Production Operator (Collection, Packaging, Inspection) *ALL SHIFTS

Director, Continuous Improvement

Manufacturing Engineer

Operations Supervisor

Quality Assurance Area Specialist II (QA for FP)

Production Supervisor - 1st Shift

Sr Associate Mfg I- Investigations

Specialist Manufacturing Investigations

Associate Manufacturing - Bulk Drug Substance Downstream - Days

Quality Assurance Area Specialist III (QA for QC)

Network Services Engineer - Hybrid 60% Remote

Production Supervisor - 2nd Shift

Associate Project Manager

Process Engineer I - Printed Packaging Material

Facilities Engineer II - Clean Utilities - PS AM

Facilities Manager

Manufacturing Associate II

Supervisor, Production

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