Jobs in the United States

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Added 1 min ago
Advanced Software Engineer - AI Reliability Engineering
General Dynamics Mission Systems, Inc
Remote, United States
…more. Our team builds purpose-built systems that replace legacy applications and establish a connected data foundation across the…
Added 1 min ago
Senior Advanced IT Network Site Reliability Engineer
General Dynamics Mission Systems, Inc
Remote, United States
Knowledge and experience in a single network domain and fully understands process applications within domain of expertise
Added 3 mins ago
AI Engineer
Blue Cross and Blue Shield of Massachusetts, Inc.
United States
Develop and integrate applications using the Google Cloud AI/ML SDKs (Vertex AI SDK for Python, Google Gen AI SDK) for programmatic access to foundation models, embeddings, tuning, and…
Added 4 mins ago
AB
Teller
Associated Bank, NA
United States
- $17 to $22.96 USD / hour
We welcome and encourage applications from all qualified parties, including but not limited to people returning to the workforce, people with disabilities, those without a college degree,…
Added 5 mins ago
Sr. Presales Systems Engineer
Forescout Technologies Inc.
United States
…or automated decision-support tools to assist with reviewing applications, assessing job-related qualifications, matching candidates to role requirements, scheduling…
Added 6 mins ago
CG
FOOD SERVICE UTILITY (FULL AND PART TIME)
Compass Group
Fairfield, CT
- $16.94 USD / hour
- Part-time
Address: Sacred Heart University - 5151 Park Ave, Fairfield, CT 06825. Note: online applications accepted only.
Added 6 mins ago
CG
COOK (FULL AND PART TIME)
Compass Group
Fairfield, CT
- $20 USD / hour
- Part-time
Address: Sacred Heart University - 5151 Park Avenue, Fairfield, CT 06825. Note: online applications accepted only.
Added 7 mins ago
AC
Technical Buyer
Aston Carter
Germantown, MD
- $83,552 to $108,618 USD / year
Added 7 mins ago
AC
Technical Planner
Aston Carter
Germantown, MD
- $83,000 to $108,000 USD / year
Added 10 mins ago
Manager, Sales Development | United States | Remote
Grafana Labs
Remote, United States
Added 10 mins ago
Manager, IT Support
iPipeline
Wayne, PA
…data libraries to accelerate, automate, and simplify various applications, processes, and workflows – from quote to commission – with seamless integration. Our vision is to help everyone…
Added 10 mins ago
Information Systems Manager
Novaspect, Inc.
Schaumburg, IL
…Technology, this leader will oversee the people and enterprise applications that support Novaspect’s business operations, including Salesforce CRM, IFS ERP, and connected systems. The…
Added 10 mins ago
SI
SAP Concur iXp Intern - Data Strategy
SAP IT Business Systeme
Bellevue, WA
- $21 to $35 USD / hour
As a leader in enterprise applications and business AI, SAP stands at the nexus of business and technology. For over 50 years, organizations have trusted SAP to bring out their best by…
Added 10 mins ago
CC
Assistant Store Manager
Community Choice Financial Family of Brands
San Jose, CA
- $22 USD / hour
Assess risk of financial transactions, evaluate, and accurately process loan/pawn applications, check cashing transactions and ancillary products.
Added 12 mins ago
IG
Platform Engineer (TS/SCI)
Insight Global
Cedar Fork, NC
- From $48 USD / hour
…Engineering & Automation • Build and maintain production automation applications that optimize platform and device management • Develop Python backends (FastAPI, Celery) and…
Added 12 mins ago
IG
Full Stack Engineering Lead
Insight Global
Boca Raton, FL
- From $78 USD / hour
…across: Salesforce CRM (Sales, Service), CPQ, Customer facing web-applications, MuleSoft APIs and Other integrations. You will leverage AI-assisted coding tools (e.g. Cursor) to accelerate…
Added 13 mins ago
Public Benefit Specialist
Ensemble RCM LLC
Bristol, TN
…accurate and appropriate submissions. Follows-up on submitted applications to insure timely billing or adjustment…
Added 14 mins ago
V
Senior Software Engineer
Virtru
Washington, DC
- $190,000 to $250,000 USD / year
We've created both a suite of powerful data protection applications and an open platform that's sparking an ecosystem of innovation. Through the Trusted Data Format (TDF) open standard,…
Added 18 mins ago
Senior Energy Engineer
ICF Resources, LLC
Houston, TX
Added 18 mins ago
Associate Operations Specialist
ICF Resources, LLC
Phoenix, AZ
Assist with processing incoming project applications.
Added 18 mins ago
Sr. Clinical Trial Associate
Liquidia
Remote, United States
…eliminate resumes during the application review process. All applications are reviewed by our recruiting team to ensure a thorough and equitable…
Added 19 mins ago
Tech Lead - Testing & Quality Assurance N 4C
Genpact LLC
United States
Furthermore, please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way.…
Added 19 mins ago
Business Development Executive 3
Genpact LLC
521 Fifth Avenue, NY
Furthermore, please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way.…
Added 19 mins ago
Business Development Executive 3
Genpact LLC
521 Fifth Avenue, NY
Furthermore, please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way.…
Added 20 mins ago
UG
Associate Director Real Estate Services - West Region - Remote
UnitedHealth Group
Cypress, CA
- $112,700 to $193,200 USD / year
Proficiency with MS Office 365 tools and applications

Actalent

Deviation Investigator

Wilson, NC, United States

$50 USD / hour

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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 2, 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 Wilson, 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 Wilson, NC. Application DeadlineThis position is anticipated to close on Nov 16, 2026. Workplace TypeThis is a fully onsite position in Wilson,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.

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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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