Visual Inspection Operator Job at Evonik Industries (Birmingham, AL)

Aerospace Source Inspector

The Source Inspector, (SI) is responsible for performing inspection operations o...

Location

United States , Carson City

Salary:

Not provided

TRIGO Global Quality Solutions

Expiration Date

Until further notice

Requirements

Experienced quality individual in dimensional and visual inspection of aerospace machined components
Experience in performing FAI’s – AS9102
Experience with hand measurement tools
Knowledge of CMM Inspection process
Knowledge and experience in GD&T (ASME Y14.5)
Knowledge and experience with blueprint interpretation
Perform final inspection and receiving inspection
MS Outlook, and EXCEL experience
Mechanical inspection experience
IPC, J-STD, and Mil-Spec inspection experience

Job Responsibility

Performing inspection operations of in-process or completed hardware, including dimensional, and visual inspection
Reviewing all paperwork relating to the product
Operations such as Final Inspection, Receiving Inspection, Outside processing, and Assembly
Verifying FAI’s to AS9102 for accuracy and completeness
Traveling to end customer’s suppliers’ locations

What we offer

12 days paid vacation first year, increasing with service years
10 days paid sick time
11 paid holidays
Healthcare insurance available: Medical, dental, vision, STD, LTD, critical illness, life insurance for self and dependents
Champ Plan Wellness and Health
Free to employees working minimum 20 hours/week with anticipated $30k/annual earnings
Participation increases net take home pay $$$ in most instances
Free wellness initiatives
Free tele-health
Free and discounted RX

Fulltime

New

Robotics Engineer - Autonomous Drone System

Meta is seeking a System Engineer to join our Infra Robotics team. This team imp...

Location

United States , Fremont, CA, or a Meta NA data-center site

Salary:

173000.00 - 245000.00 USD / Year

Quality Inspector

We are seeking a skilled and detail-oriented Quality Inspector to join our team....

Location

United States , Hollywood

Salary:

Not provided

Coherent Technical Services

Expiration Date

Until further notice

Requirements

Minimum of 3 years of experience in quality inspection within a manufacturing environment
Proficiency in operating Coordinate Measuring Machines (CMM) and Inspection Arm/Scanner is preferred
Strong knowledge and understanding of ISO9001/2015 and AS9100D standards
Familiarity with inspection techniques, tools, and equipment such as calipers, micrometers, height gauges, gauging fixtures, etc.
Ability to interpret engineering drawings, specifications, and technical documentation
Detail-oriented with excellent analytical and problem-solving skills
Strong organizational and time management abilities to handle multiple inspection tasks and meet deadlines
Excellent verbal and written communication skills
Ability to work independently and as part of a team
Proficiency in using computer software for data entry, analysis, and report generation

Job Responsibility

Perform thorough inspections of incoming materials, in-process components, and finished products to verify conformance with specifications and quality standards
Utilize measuring tools, such as calipers, micrometers, height gauges, and gauging fixtures, to conduct accurate and precise measurements
Operate Coordinate Measuring Machines (CMM) and Inspection Arm/Scanner to inspect complex parts and assemblies
Conduct visual inspections to identify any defects, abnormalities, or non-conformities in products or materials
Document inspection results and maintain accurate records of inspections, including detailed reports and data analysis
Collaborate with the Quality Assurance team to identify areas for improvement and implement corrective actions to address non-conformities
Participate in root cause analysis investigations to determine the cause of quality issues and assist in implementing effective preventive measures
Ensure compliance with ISO9001/2015 and AS9100D standards and actively contribute to maintaining and improving the quality management system
Communicate effectively with production personnel, engineers, and other stakeholders to address quality concerns and provide guidance on quality requirements
Stay updated on industry best practices, new inspection techniques, and emerging quality standards

New

Visual Inspection Technician I

This position is responsible for performing visual inspection of sterile filled ...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Previous employment within an FDA/USDA, GMP environment is desired
High school diploma or equivalent required
Basic computer skills are required
Basic verbal and written skills
Able to understand and follow instructions
Ability to read, understand, follow, and comply with technical and written documents (SOPs) written in English
Must be able to maintain visual qualifications: (20/20 vision corrected or uncorrected checked annually)
ability to see all colors and the ability to visually discern product specifications across multiple products
Must be able to work while wearing PPE for all GMP areas for an entire shift (Includes non-latex gloves, hair/beard covers and lab coats)
Detail oriented, and self-motivated

Job Responsibility

Performing visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives
Ensure finished drug product vials manufactured by PCI are free of visible defects which are culled through the visual inspection process to support patient safety and product quality
Repetitive handling of sterile filled containers while primarily in a seated position, swirling and inverting containers and extending arm out in front of light source in order to identify product defects
Records production quantities and other applicable information with adherence to Good Documentation Practices
Applies a moderate level of math skills to include piece counting, time calculations, and product reconciliation
Following written procedures and documents results in a neat and accurate manner according to GMP standards and other regulations
Performs daily cleaning of visual inspection and packaging areas in accordance with established procedures
Identifies and communicates product quality issues
Maintains attention to detail and quality while completing multiple or repetitive tasks and meeting product timelines
Effectively communicates both verbally and in writing with all levels

Fulltime

New

Visual Inspection Technician

This position is responsible for performing visual inspection of sterile filled ...

Location

United States , Madison

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Previous employment within an FDA/USDA, GMP environment is desired
High school diploma or equivalent required
Basic computer skills are required
Basic verbal and written skills
Able to understand and follow instructions
Ability to read, understand, follow, and comply with technical and written documents (SOPs) written in English
Must be able to maintain visual qualifications: (20/20 vision corrected or uncorrected checked annually)
ability to see all colors and the ability to visually discern product specifications across multiple products
Must be able to work while wearing PPE for all GMP areas for an entire shift (Includes non-latex gloves, hair/beard covers and lab coats)
Detail oriented, and self-motivated

Job Responsibility

Perform visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives
Ensure finished drug product vials manufactured by PCI are free of visible defects which are culled through the visual inspection process to support patient safety and product quality
Repetitive handling of sterile filled containers while primarily in a seated position, swirling and inverting containers and extending arm out in front of light source in order to identify product defects
Records production quantities and other applicable information with adherence to Good Documentation Practices
Applies a moderate level of math skills to include piece counting, time calculations, and product reconciliation
Following written procedures and documents results in a neat and accurate manner according to GMP standards and other regulations
Performs daily cleaning of visual inspection and packaging areas in accordance with established procedures
Identifies and communicates product quality issues
Maintains attention to detail and quality while completing multiple or repetitive tasks and meeting product timelines
Effectively communicates both verbally and in writing with all levels

Fulltime

Processor/assembler/production

Come join a global leader in pipe joining solutions! Victaulic has what you’re l...

Location

United States , Forks Township, PA

Salary:

Not provided

Victaulic

Expiration Date

Until further notice

Requirements

Operate, monitor and inspect assembly machines, tools, dip tanks, paint lines, impregnators, and other related equipment
Perform minor troubleshooting
Operate all necessary moving, hauling and storing equipment
Know and follow proper safety procedures and wear prescribed safety equipment
Report work performed, findings or results of inspections, and time and materials used
Maintain work area in neat and clean condition
Report immediately any injury, unsafe act or condition, or any failure or impending failure of plant equipment
Perform duties to assure uninterrupted operation of the facility
Actively participate in SRP, VPDS, and any other Company initiative
Inspect castings visually and dimensionally

Job Responsibility

Aid in the manufacture and shipment of quality products by means of transferring, cleaning, painting (painting to include plant equipment, guard rails, floor lines, storage racks, conveyors, production offices, locker rooms, rest rooms, and related equipment within the production areas), removing, sweeping, shoveling, inside or outside, of our facilities
Aid and assist in all related activities, to relieve other employees for breaks, injuries, sickness, tardiness, absenteeism, or vacation/personal days
Pack, inspect, prepare for shipment/transfer all products and/or material as necessary

What we offer

Company Matched 401k Plan
Comprehensive Healthcare Benefits
Employee Assistance Program
Education Assistance / Tuition Reimbursement Program
Wellness Program
Medical
Vision
Dental
Prescription
Disability

Fulltime

Senior Subsea Pipeline Marine Inspector

Airswift are a Global Manpower Provider specializing in the Energy, Infrastructu...

Location

Qatar , Doha

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Bachelor’s degree in engineering discipline (Mechanical) with demonstrated knowledge and experience
CSWIP 3.4UC Underwater Inspection Controller (Ref. CSWIP Document No.CSWIP-DIV-7-95 – Part 2)
Current / valid BOSIET, TBOSIET, FOET or TFOET certificate (Ref. OPITO requirements), as applicable, in conjunction with an offshore medical certificate
Experience in conducting QMS audits and QA verification programs for various project phases (i.e., Engineering, Procurement, Construction and Installation (specifically, the Repair / Installation of pipelines and their associated infrastructure) would be preferable
At least six (6) years of working experience in Quality Assurance and Control (QA/QC) within the Oil and Gas industry (i.e., onshore and offshore)
Should have a proven history as a lead 3.4UC underwater inspection controller within demanding subsea/offshore projects
Subsea pipeline project experience is highly desired, with emphasis on pipeline operations, integrity assurance/non-destructive testing (NDT) and inspection, maintenance and/or design and construction
Familiarity with marine vessel operations and the organisational responsibility of the (i) Offshore Construction/Installation Manger, (ii) Vessel Master, (iii) Diving and ROV Supervisors, (iv) Client Representative(s), (v) Certifying Authorities, etc.
Knowledge and working experience of underwater inspection (UWI) in the form of visual inspection and non-destructive testing (NDT) conducted by means of the intervention of diver(s) and/or remotely operated vehicle (ROV) or crewed submersible (i.e., either as a practitioner and/or as the result of training or certification conforming to the requirements of CSWIP Document No. CSWIP-DIV-7-95 – Part 1 and 2)
With respect to UWI and other related activities, shall be familiar with (i) relevant subsea applied inspection systems, (ii) recording and processing of data, (iii) quality assurance (QA), (iv) inspection planning and briefing, (v) the capabilities and limitations of divers/ROV’s and submersibles, and (vi) the care and deployment of equipment

Job Responsibility

Ensure compliance with QatarEnergy LNG systems and processes, including the Project Management System. Engage contractors and applicable third-party organisations with a professional approach and maintain a good working level relationship
Have a knowledge of the front end engineering design (FEED) deliverables and engineering study reports to support the implementation of the Project Quality Plan (PQP) and associated Procedures
Review the project Scope of work, to determine the nature, extent, and frequency of quality verification activities
Monitor, evaluate and report the inspection and testing status of the pipeline repair activities
Maintain interface relationships with Subsea Pipeline Repair Installation, and Inspection Contractors (including nominated specialist third-party Contractor organisation(s)), and the applicable regulatory focal points
especially, those functioning offshore
Review Contractor’s and Vendor’s quality reports / deliverables, in line with the project quality requirements
In conjunction with the QA/QC delegation operating offshore, verify that the repair activities are in accordance with approved documented information (i.e. procedures, specifications, detailed methodologies, etc)
Support the underwater inspection (UWI) activities during the offshore / subsea repairs, by means of the development of job records, preparation of daily reports, review of diver commentary and transfer into the written form, interpretate ROV camera footage and transfer into the written form and be able to produce an oral commentary of the daily activities, as and when required
Monitor the technical inspections, verification, certification and acceptance by Specialist Third Party Inspection (TPI) Contractor, as applicable, and develop the final documentation for each offshore campaign (i.e., PL-49, PL-75, PL-610 and PL-811)

Fulltime

New

QA Specialist II - Operations

The QA Operations Specialist II – Floor Support is responsible for providing QA ...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a relevant scientific field
Minimum 3 years’ experience in relevant GMP industry, with minimum 1 year experience in Quality, or Equivalent combination of education and experience
ASQ certification is a plus
Exposure to RCA, technical writing, and working with quality related investigations
Exposure to lean operation excellence highly desirable
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH
Knowledge and ability to apply basic scientific principles to solve operational, as well as routine quality tasks
Experience using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9

Job Responsibility

Perform QA on-the-floor activities supporting client projects, including room release, auditing critical processes, reviewing GMP documentation in real time, and resolving issues that occur during manufacturing
Consult with internal teams such as Operations, QC, Facilities/Engineering, Project Management, and Materials Management to resolve complex situations or problems
Perform frequent walkthroughs and internal audits of manufacturing and support areas to ensure adherence to policies and procedures
Batch record review for adherence to internal procedures and Good Documentation Practices
Support the evaluation and disposition of intermediates, finish bulk drug substance and drug product
Review, approval and disposition of incoming materials such as consumables, excipients, and Active Pharmaceutical Ingredient
QA review and approval of new and revised GMP documents such as SOP’s and raw material specifications
Act as first responder for on the floor quality issues in a timely manner, documentation of all events/investigations and required immediate corrective actions
Co-ownership of nonconforming material investigations
Review of Quality Control environmental and utility monitoring data and test results

Fulltime

Visual Inspection Operator

Evonik Industries

Location:
United States , Birmingham, AL

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 20, 2026

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Visual Inspection Operator

Evonik Industries

Location:United States , Birmingham, AL

Category:Manufacturing

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 20, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

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