Jobs in the United States

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AF
Administrative Assistant for Residential Department
ABILITIES FIRST, INC
Poughkeepsie, NY
- $18.62 to $20.62 USD / hour
…coordinating office activities, maintaining records and tracking systems, supporting departmental projects, and serving as a key point of contact for staff and…
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Director REMS Operations 1
Teva Pharmaceutical
West Chester
Experience with software systems, call center technologies
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Construction Manager II
AFL
Dallas, TX
Knowledge of electrical, fiber, structured cabling, low-voltage, and network infrastructure systems.
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Construction Manager II
AFL
Atlanta, GA
Knowledge of electrical, fiber, structured cabling, low-voltage, and network infrastructure systems.
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Director of Quality
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MI
With the primary focus on deploying RealTruck Quality Management Systems (QMS), improving customer satisfaction, and reducing Cost of Poor Quality (COPQ), the Director will drive and…
Added 1 min ago
Welder lead
Brown & Root
Sulphur, LA
Lays out, fabricates, assembles, installs and maintains piping systems, pipe supports, fixtures, and related hydraulic and pneumatic equipment for steam, hot water fixtures and equipment…
Added 1 min ago
Pipefitter Lead
Brown & Root
Sulphur, LA
Lays out, fabricates, assembles, installs and maintains piping systems, pipe supports, fixtures, and related hydraulic and pneumatic equipment for steam, hot water fixtures and equipment…
Added 1 min ago
Sr. Manager - Talent Development Training
Arthrex
Naples, FL
8 years of people leadership experience required
Added 1 min ago
Quality Manager (Medical Device Contract Manufacturing)
Cadence Inc
Sturgeon Bay, WI
Ensure compliance with applicable FDA regulations, ISO standards, customer requirements, and internal quality management systems.
Added 1 min ago
Production Supervisor - CAM - CCM
Carlisle
Acworth, Georgia, GA
We deliver roofing, insulation, waterproofing, and architectural systems for commercial and residential projects using a focus on innovation and continuous improvement to solve today’s…
Added 1 min ago
Production Supervisor - CAM - CCM
Carlisle
Baltimore, Maryland, MD
We deliver roofing, insulation, waterproofing, and architectural systems for commercial and residential projects using a focus on innovation and continuous improvement to solve today’s…
Added 1 min ago
UO
Success Coach - Virtual School K-5th (Part-Time)
UCP of Central Florida
Orlando, FL
- $15 to $16 USD / hour
- Part-time
The candidate must have access to reliable high speed internet
Added 1 min ago
UO
Teacher - Virtual School K-5th
UCP of Central Florida
Orlando, FL
- $49,000 to $52,000 USD / year
The candidate must have access to reliable high speed internet
Added 1 min ago
IC
Production Supervisor - Lincoln Ave - Utica, NY
Indium Corporation
Utica, NY
- $20 to $32.75 USD / hour
Access computer systems to complete all required documentation to track work, record scrap, and maintain accurate records of completed parts and required inventory
Added 1 min ago
Systems Analyst II
Northern Technologies Group
United States
Northern Technologies Group (NTG) is seeking a qualified Systems Analyst II to support the Department of Defense Chief Information Officer (DoD CIO) within its Special Access Program…
Added 2 mins ago
Restaurant Operations Manager
Messiah University
Mechanicsburg, PA
Maintain computer software systems for the daily running of each operation (Blackboard, C-Bord, Word, Excel, Publisher, Powerpoint, and Touch Screen System).
Added 2 mins ago
PROCUREMENT SUPERVISOR
State of Maryland
MD
Added 2 mins ago
Reliability Engineer- Fiber Esters & Acid Con
Eastman
Kingsport, TN
Identify and prioritize opportunities for reliability improvements by mining information from SAP, reliability systems, and production logs
Added 2 mins ago
Senior Engineer, Substation Engineering and Design(Hybrid Schedule)
Eversource Energy Service Company
Berlin, CT
…modifications, and replacements to the transmission and distribution systems are completed accurately and in accordance with internal and industry…
Added 2 mins ago
Senior Advisor, Safety, Gas
Eversource Energy Service Company
Waterbury, CT · Norwalk, CT · East Windsor, CT
Knowledge of Distribution operations and associated electrical, gas systems, construction practices and renewable energy practices is highly desired.
Added 2 mins ago
Manager, Electric Operations
NSTAR Electric DBA Eversource Energy
United States
Manages overhead and underground work crews on a 24 hour, 7-day per week basis to execute these processes · Must have a strong knowledge of computers and related technology and have the ability to learn and utilize available information technologies
Added 2 mins ago
LI
HVAC Service Technician
Lennox International
Pelham, AL
- $39,000 to $77,000 USD / year
…and servicing of heating, ventilating and air conditioning systems for commercial…
Added 3 mins ago
Warehouse Associate- SAN Wet Plant B-Shift
( ) Simmons Foods
Siloam Springs, AR
…possible within the larger organization. Simmons operating systems principles and objectives: Is familiar with Simmons' established operating systems (e.g. quality, security, office…
Added 3 mins ago
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Process Engineer
Alstom
Plattsburgh, NY
- $70,000 to $90,000 USD / year
At Alstom, we build what millions depend on daily - rail transportation systems that can't afford to fail. We're more than 85,000 people worldwide creating the industry's most diverse…
Added 3 mins ago
Facilities Project Engineer
Tesla Laboratories. Inc.
Honolulu, HI
…lifecycle management of complex facilities and infrastructure…

Actalent

Deviation Investigator

Greenville, NC, United States

$50 USD / hour

Apply on careers.actalentservices.com About employer

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Job details

Pay: $50 USD / hour
Experience: At least 2 years of experience working in a pharmaceutical environment performing investigations under Good Manufacturing Practice (GMP) requirements.
Posting language: English
Posted: Nov 12, 2026

Original job description

Job Title: Deviation InvestigatorJob DescriptionThe Deviation Investigator identifies, documents, investigates, and resolves deviations from standard procedures, protocols, and regulatory requirements within a pharmaceutical environment. This role ensures that all deviations are managed in compliance with internal policies and industry regulations, and that corrective and preventive actions (CAPAs) are effectively developed, implemented, and monitored. The Deviation Investigator supports continuous improvement by analyzing deviation trends and contributing to process enhancements across the organization.

Responsibilities

Identify and document deviations from standard operating procedures (SOPs), quality standards, and regulatory guidelines in a timely and accurate manner.
Conduct thorough, structured investigations to determine the root cause of deviations, using established methodologies such as fishbone diagrams and 5 Whys.
Collaborate with cross-functional teams to develop robust corrective and preventive actions (CAPAs) that address identified root causes and prevent recurrence.
Implement and track CAPAs, ensuring actions are completed on schedule and verified for effectiveness.
Maintain accurate, detailed, and compliant records of all deviations, investigations, and CAPAs in accordance with Good Documentation Practices (GDP).
Prepare clear and comprehensive written investigation reports suitable for internal review and potential regulatory inspection.
Present deviation findings, investigation outcomes, and CAPA status to stakeholders and, when required, to regulatory authorities.
Ensure all deviation management activities align with company policies, Good Manufacturing Practices (GMP), and applicable regulatory requirements.
Participate in internal and external audits and inspections by providing complete and accurate documentation and responding to questions related to deviations and investigations.
Analyze deviation trends and metrics to identify systemic issues, recurring problems, and opportunities for process improvement.
Contribute to and support continuous improvement initiatives aimed at strengthening quality systems and reducing deviation occurrence.
Participate in training programs to enhance knowledge and skills related to deviation management, root cause analysis, and quality assurance.
Conduct investigations in aseptic environments, including work on isolator lines, ensuring adherence to aseptic techniques and contamination control practices.
Support process improvement efforts by providing insights from deviation investigations and recommending enhancements to procedures, processes, and controls.

Essential Skills

At least 2 years of experience working in a pharmaceutical environment performing investigations under Good Manufacturing Practice (GMP) requirements.
Strong knowledge of GMP principles and their practical application to deviation management and quality systems.
Demonstrated proficiency in root cause analysis, including hands-on experience using fishbone diagrams and 5 Whys methodologies.
Proven technical writing skills with experience authoring clear, detailed, and compliant investigation reports.
Experience conducting investigations in an aseptic environment, including work on isolator lines.
Strong analytical and problem-solving abilities with a structured approach to identifying and resolving issues.
Ability to interpret and apply standard operating procedures (SOPs), quality standards, and regulatory guidelines.
High attention to detail and accuracy in documentation in alignment with Good Documentation Practices (GDP).
Effective collaboration skills to work with cross-functional teams during investigations and CAPA development.

Additional Skills & Qualifications

Experience with process improvement initiatives related to quality systems or manufacturing operations.
Familiarity with continuous improvement methodologies and tools used to reduce deviations and enhance process robustness.
Comfort presenting investigation findings and CAPA plans to stakeholders and supporting audit and inspection activities.
Ongoing commitment to professional development through training in deviation management, quality assurance, and related topics.

Work EnvironmentThis role operates in a regulated pharmaceutical environment with a focus on GMP and aseptic processing. The standard work schedule is Monday through Friday from 8:00 a.m. to 5:00 p.m., with flexibility to accommodate business needs. Approximately 10 hours of overtime per week are expected. The position is offered as a 12-month contract with substantial opportunity for conversion to a permanent role based on performance and business requirements. Interviews are conducted face to face. The work involves frequent interaction with documentation systems, quality systems, and cross-functional teams, as well as time spent in aseptic areas and on isolator lines, following appropriate gowning and contamination control practices. Job Type & LocationThis is a Contract position based out of Greenville, NC. Pay and BenefitsThe pay range for this position is $50.00 - $50.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of Greenville, NC. Application DeadlineThis position is anticipated to close on Nov 20, 2026. Workplace TypeThis is a fully onsite position in Greenville,NC.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Apply on careers.actalentservices.com About employer

More about this job

Skills

Documentation
Inspection
Good manufacturing practices
Process improvement
Quality control systems
Root cause analysis
Quality assurance
Technical writing
Problem solving
Attention to detail
Collaboration

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Work requirements

Jobs in the United States