Deviation investigation remediation experience is a plus but is not necessary. * Undergraduate Engineering/STEM degree preferred (mechanical, chemical, biomedical, etc.). * 0-3 years experience. Some ...
Deviation investigation remediation experience is a plus but is not necessary. * Undergraduate Engineering/STEM degree preferred (mechanical, chemical, biomedical, etc.). * 0-3 years experience. Some ...
The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised ...
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The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised ...
The Deviation Investigator/Initiator is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised ...
Quick apply
The Deviation Investigator/Initiator is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised ...
Manufacturing Deviations Investigator
Portsmouth, NH ยท On-site
$30 - $45/hr
Onsite Summary Deviation Investigator Level I-III / Manufacturing Deviations Investigator is responsible for investigating and completing deviation cases to identify root causes and implement ...
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Manufacturing Deviations Investigator
Portsmouth, NH ยท On-site
$30 - $45/hr
Onsite Summary Deviation Investigator Level I-III / Manufacturing Deviations Investigator is responsible for investigating and completing deviation cases to identify root causes and implement ...
Deviation Writer
Indianapolis, IN ยท On-site
We are seeking an experienced Deviation Writer to support investigation writing and root cause analysis within a GMP-regulated manufacturing environment. This role partners with Manufacturing ...
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Deviation Writer
Indianapolis, IN ยท On-site
We are seeking an experienced Deviation Writer to support investigation writing and root cause analysis within a GMP-regulated manufacturing environment. This role partners with Manufacturing ...
Deviation Writer
Bloomington, IN ยท On-site
This role will be responsible for authoring high-quality deviation investigations, performing root cause analysis, and collaborating with cross-functional teams to ensure timely and compliant ...
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Deviation Writer
Bloomington, IN ยท On-site
This role will be responsible for authoring high-quality deviation investigations, performing root cause analysis, and collaborating with cross-functional teams to ensure timely and compliant ...
Deviation Investigations Specialist
Davie, FL ยท On-site
$33 - $35/hr
The Investigator I authors and coordinates high-quality investigations for events occurring in ... g., deviation/CAPA systems, MES, LIMS, historian/trending tools, AI tools) to support ...
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Deviation Investigations Specialist
Davie, FL ยท On-site
$33 - $35/hr
The Investigator I authors and coordinates high-quality investigations for events occurring in ... g., deviation/CAPA systems, MES, LIMS, historian/trending tools, AI tools) to support ...
Deviation Investigations Specialist
Davie, FL ยท On-site
$32 - $35/hr
Deviation Investigations Specialist 6 Months (possible extension) Davie, FL 100% Onsite - looking ... The Investigator I authors and coordinates high-quality investigations for events occurring in ...
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Deviation Investigations Specialist
Davie, FL ยท On-site
$32 - $35/hr
Deviation Investigations Specialist 6 Months (possible extension) Davie, FL 100% Onsite - looking ... The Investigator I authors and coordinates high-quality investigations for events occurring in ...
POSITION OVERVIEW Conduct and write formal investigation of process deviations for Manufacturing ... Work independently to comply with procedure driven guidelines relating to deviation and complaint ...
POSITION OVERVIEW Conduct and write formal investigation of process deviations for Manufacturing ... Work independently to comply with procedure driven guidelines relating to deviation and complaint ...
Deviation Writer Location: Fishers, IN Job Summary Seeking an experienced Deviation Writer to ... Write and investigate GMP deviations, non-conformances, and quality events. * Gather facts, review ...
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Deviation Writer Location: Fishers, IN Job Summary Seeking an experienced Deviation Writer to ... Write and investigate GMP deviations, non-conformances, and quality events. * Gather facts, review ...
QC Deviation Specialist III
Springfield, MO ยท On-site
$45 - $47/hr
Perform and document Deviation Investigations for Manufacturing and Quality Control operations. * Conduct Root Cause Analyses (RCA) and determine appropriate Corrective and Preventive Actions (CAPAs ...
QC Deviation Specialist III
Springfield, MO ยท On-site
$45 - $47/hr
Perform and document Deviation Investigations for Manufacturing and Quality Control operations. * Conduct Root Cause Analyses (RCA) and determine appropriate Corrective and Preventive Actions (CAPAs ...
Perform deviation associated activities for Deviation Management group writers for VBF and VMF Make ... S. degree in appropriate engineering/scientific field Previous experience in writing investigations ...
Perform deviation associated activities for Deviation Management group writers for VBF and VMF Make ... S. degree in appropriate engineering/scientific field Previous experience in writing investigations ...
QA Technical Writer/Investigator
Baltimore, MD ยท On-site
$45 - $70/hr
We are actively recruiting 4 QA Deviation Technical Writers for a 6+ month on-site quality remediation project. Responsibilities: * In this role you will draft comprehensive deviation investigation ...
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QA Technical Writer/Investigator
Baltimore, MD ยท On-site
$45 - $70/hr
We are actively recruiting 4 QA Deviation Technical Writers for a 6+ month on-site quality remediation project. Responsibilities: * In this role you will draft comprehensive deviation investigation ...
Senior Manager, Deviation Management - Quality Assurance
Conshohocken, PA ยท On-site
$147K - $180K/yr
Coaches teams on investigation quality expectations and effective prevention actions. Key Responsibilities Process Ownership & Governance * Own deviation standards, templates, training expectations ...
Senior Manager, Deviation Management - Quality Assurance
Conshohocken, PA ยท On-site
$147K - $180K/yr
Coaches teams on investigation quality expectations and effective prevention actions. Key Responsibilities Process Ownership & Governance * Own deviation standards, templates, training expectations ...
Coaches teams on investigation quality expectations and effective prevention actions. Key Responsibilities Process Ownership & Governance * Own deviation standards, templates, training expectations ...
Coaches teams on investigation quality expectations and effective prevention actions. Key Responsibilities Process Ownership & Governance * Own deviation standards, templates, training expectations ...
Key Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
Key Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
Principal Scientist Deviation Management Lilly Medicine Foundry
Lebanon, IN ยท On-site
$65.25 - $169.40/hr
Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
New
Principal Scientist Deviation Management Lilly Medicine Foundry
Lebanon, IN ยท On-site
$65.25 - $169.40/hr
Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
New
Key Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
Key Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
Key Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
Key Responsibilities Deviation Investigation Leadership * Lead deviation and out-of-specification (OOS) investigations (Minor, Major, Critical), applying structured root cause analysis methods (5-Why ...
Deviation Management Specialist - I (Assistant)
West Point, PA ยท On-site
$86K/yr
The Deviation Management Contractor will be responsible for technical support to vaccine ... The primary responsibility of the individual will be investigation initiation and closure ...
Deviation Management Specialist - I (Assistant)
West Point, PA ยท On-site
$86K/yr
The Deviation Management Contractor will be responsible for technical support to vaccine ... The primary responsibility of the individual will be investigation initiation and closure ...
Deviation Investigator information
See salary details
$32K - $41K
7% of jobs
$41K - $50K
14% of jobs
$51.5K is the 25th percentile. Wages below this are outliers.
$50K - $59K
24% of jobs
The median wage is $63.5K / yr.
$59K - $68K
9% of jobs
$68K - $77K
5% of jobs
$77K - $86K
15% of jobs
$86.8K is the 75th percentile. Wages above this are outliers.
$86K - $95K
3% of jobs
$95K - $104K
6% of jobs
$104K - $113K
4% of jobs
$113K - $122K
12% of jobs
$122K - $131K
0% of jobs
$32K
$75.3K
$131K
How much do deviation investigator jobs pay per year?
What does a deviation investigator do?
A typical day for a Deviation Investigator involves reviewing deviation reports, gathering data from production or laboratory records, and conducting interviews with staff to determine the root cause of incidents. You will document findings in compliance with standard operating procedures and collaborate closely with cross-functional teams, such as manufacturing, quality assurance, and regulatory affairs, to recommend corrective and preventive actions. Many Deviation Investigators participate in regular meetings to discuss ongoing cases and share best practices. The role requires excellent organizational skills to manage multiple investigations concurrently while ensuring timely and thorough resolution.
What is a deviation investigator?
A Deviation Investigator is responsible for analyzing deviations in manufacturing, quality control, or laboratory processes within industries like pharmaceuticals or biotechnology. They identify root causes, document findings, and implement corrective and preventive actions (CAPAs) to ensure compliance with regulatory standards. Their role is crucial in maintaining product quality, safety, and adherence to Good Manufacturing Practices (GMP). Effective communication, problem-solving skills, and knowledge of industry regulations are essential for this position.
What are the key skills and qualifications needed to thrive as a deviation investigator?
To thrive as a Deviation Investigator, you need a strong background in quality assurance or compliance, along with experience in root cause analysis and deviation management, often supported by a degree in a scientific or technical field. Familiarity with industry regulations (such as GMP or ISO standards), quality management systems (QMS), and tools like TrackWise or MasterControl is highly desirable. Strong analytical thinking, attention to detail, effective communication, and the ability to work collaboratively are key soft skills for this role. These skills ensure accurate investigation, thorough documentation, and prompt resolution of deviations to maintain product quality and regulatory compliance.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 5 days ago
Job description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
- We empower and support our colleagues
- We commit to client success at every turn
- We have the courage to do the right thing
- We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
- We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Responsibilities:
Entry level CQV Engineer position in the Pharma industry. Client will train the resource on Deviation Investigation.
Requirements
- Deviation investigation remediation experience is a plus but is not necessary.
- Undergraduate Engineering/STEM degree preferred (mechanical, chemical, biomedical, etc.).
- 0-3 years experience. Some Pharma experience preferred but not absolutely required. New college grads with internship experience encouraged to apply
- Proficiency using PC and Microsoft Office tools.
- Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms.
- Ability to work as part of a team.
- Strong problem-solving and critical thinking skills.
- Excellent organizational and time management skills.
- Strong attention to detail
- Strong interpersonal skills and clear communication capabilities.
- Experience with and tolerance for high levels of challenge and change.
Benefits
Why Choose Verista?
- High growth potential and fast-paced organization with a people-focused culture
- Competitive pay plus performance-based incentive programs
- Company-paid Life, Short-Term, and Long-Term Disability Insurance.
- Medical, Dental & Vision insurances
- FSA, DCARE, Commuter Benefits
- Supplemental Life, Hospital, Critical Illness and Legal Insurance
- Health Savings Account
- 401(k) Retirement Plan (Employer Matching benefit)
- Paid Time Off (Rollover Option) and Holidays
- As Needed Sick Time
- Tuition Reimbursement
- Team Social Activities (We have fun!)
- Employee Recognition
- Employee Referral Program
- Paid Parental Leave and Bereavement
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com
About Verista
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
201 - 500 Employees
Headquarters location
Fishers, IN, US
Year founded
2020