Deviation investigator

SGS_JOB_1658

Scientific
 Texas
Deviation
investigation
capa
documentation

Contract - 6 months

Location ; Houston TX. 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 completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence

Job Responsibilities:

  • Technical writing for the educated but uninformed reader, translate difficult and complex scientific events into a brief and cohesive report as a finished product. Accurately capture immediate actions and containment of the event, address comments from both internal and external clients on the compiled final report.
  • Gathering Data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation, assessment of event for impact to Safety Identity Strength Quality Purity (SISQP), perform trending analysis, identification of Corrective and Preventative Actions to reduce deviation recurrence, performance of Risk Assessments, Causing Mapping, Interviewing.
  • Management of multiple projects and timelines concurrently. Ability to adhere to standard timeline and escalate actions appropriately for resolution in a timely manner. Participation in the Daily Management meetings to update leadership or current deviation statuses.
  • Routine interaction with the customer, including compilation of Power Points to communicate investigational current status, Alignment meetings, facilitated reviews, CAPA discussions, Comments resolution.
  • Work on the manufacturing floor for data gathering, observing of processes for investigations, and performance of associate interviews.
  • Meeting Facilitation and participation, aligning internal review team and area subject matter experts on an agreed to investigational path forward. Complex Conflict resolution, problem solving in a cross functional setting, and ability to keep the meeting on track to achieve objectives of varying difficulty. Attendance and occasional leadership of the daily management system and participating/leading the deviation review board.
  • Perform other duties as assigned.

Skills:

  • Investigations
  • CAPA
  • Root Cause Analysis (RCA)  

Education/Experience:

  • Root Cause Analysis (RCA)

Related Jobs

Field Service Technician II

Scientific
 Illinois
6 Months

Location (mandatory): Chicago, IL The Video team is responsible for designing, implementing, and supporting video solutions across the City. The team partners with multiple city agencies to define requirements and deliver solutions that increase situational awareness for mission critical first responders.

IP Camera
AV
Linux
Windows
Technical Support

Laboratory Technician I

Scientific
 Florida
10 months + (Temp to Perm based on performance and openings)

Location (mandatory): 3340 Enterprise Way, Miramar, FL 33025 The Laboratory Technician is responsible for ensuring timely, accurate, and comprehensive processing during screening, admission, study conduct, and discharge procedures. The role supports clinical and laboratory operations while ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory standards.

Laboratory Processing
Vital Signs
ECG
Specimen Aliquoting
MS Office
Communication Skills
Time Management
Attention to Detail

Bench Scientist – I (Entry level)

Scientific
 New York
$40-$45/hr on w2
12 Months Contract

Location (mandatory): Pearl River, NY 10965. This is a laboratory-based position within the Vaccines Early BioProcess Analytical Development group. The role supports early vaccine development through routine sample testing, analytical method development, and assay qualification studies. The position is highly hands-on, fast-paced, and focused on supporting high-visibility vaccine projects through extensive bench work.

ELISA
Plate-based assays
Sample testing
Analytical method development
Electronic Laboratory Notebook (ELN)
Data analysis

Entry level Laboratory Technician

Scientific
 Utah
04 months + (Highest possibilities of extension)

Location: 4745 Wiley Post Way Salt Lake City, UT 84116 Small Description: This is an entry level position. Shift Schedule: Monday - Friday 8:00am - 5:00pm. Job ID: TEVAJP00009751. Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. Focus on candidates who have hands-on bench and laboratory experience (including academic or internship lab work), with exposure to sample preparation, routine testing, and documentation in a lab setting. Prioritize early-career profiles, such as associate-degree level candidates or students currently in school or taking a short break.

Experience with inventory management
Associate's degree in Science or related field.
Someone with minimum experience. As an example
someone who has had Lab Chemistry 1 experience.

Research Associate – III

Scientific
 New York
$45 - $47/hr on W2.
01 Year + (Highest possibilities of extension)

Location (mandatory): 66 Hudson Yards Blvd East, New York, NY 10001 (Hybrid) Small Description: This is a full-time, 12-month Contractor/Research Associate (RA) position on the HTA, Value & Evidence (HV&E) Thoracic & Precision Medicine Oncology team within the Global Access & Value (GAV) organization. The Research Associate will provide technical support, analysis, and reporting for assets at various stages of development within the Economics and Outcomes Research (HEOR) function. Interview Schedule: Two rounds of interviews will be conducted: an initial screening interview followed by a team interview.

HEOR
Real-World Data Studies
Literature Review
Evidence Synthesis
Cost-Effectiveness Analysis
Economic Modeling
Patient-Reported Outcomes
Database Analysis (Claims & EMR)
PowerPoint
Excel
Project & Vendor Management
SharePoint

Medical Writer II

Scientific
Remote
10 Months (Contract, possibilities of extension

Health Care Copywriter (Digital & Media Content) This fully remote role is for a Health Care Copywriter who creates compliant, engaging digital and media content for both HCP and consumer audiences. You’ll translate clinical data and approved claims into clear messaging across ads, social, emails, video scripts, and partner platforms, while working closely with designers, marketers, and regulatory teams. The job requires 3+ years of healthcare copywriting experience, comfort with MLR processes, attention to detail, and the ability to leverage GenAI tools to accelerate content without compromising accuracy or compliance.

Digital & Media Content
MLR
GenAI tools
HCP
Healthcare copywriting

QC Analyst I

Scientific
 California
27.93
06 months

Location (mandatory): Vacaville California With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.

laboratory testing
trend analysis
documentation review
cGMP regulations

Manufacturing Associate - Biotech

Scientific
 California
27.50
12 Months

Location (mandatory): Vacaville CA The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

GMP
Manufacturing environment
Laboratory tools

Core Technician

Scientific
 Texas
12 months

Location (mandatory): Houston TX The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be responsible for maintaining, stocking, and set-up of clean room environment.

Environmental monitoring
GMP
documentation
logo

At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.


2025. All right reserved.
logologologologo