Auditing Power BI Chemistry TrackWise

CareerCircle
Berkeley, United States of America
yesterday

Role details

Contract type
Temporary to permanent
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Intermediate
Compensation
$ 80K

Job location

Berkeley, United States of America

Tech stack

Microsoft Word
Microsoft Excel
Agile Methodologies
Artificial Intelligence
Continuous Integration
Data Centers
Linux
Python
PostgreSQL
MySQL
Microsoft PowerPoint
Power BI
Software Engineering
SQL Databases
Tableau
Smartsheet
Grafana
Information Technology
Trackwise
Programming Languages

Job description

The Quality Investigator/Scientist II will operate in a high-throughput environment, completing investigations on behalf of various QC testing groups. This role requires leading multiple investigations simultaneously, ensuring on-time completion through dedication and collaboration with partners in QA and the testing groups. As a strong individual contributor, you will maintain a steady record closure rate while working on moderate complexity investigations and assist more junior investigators when needed. Participation in QC compliance activities related to audits and continuous improvement is also expected., * Stay current with training in Success Factors.

  • Conduct RAPID meetings with QA and QC staff occasionally.
  • Use TrackWise software to author investigations.
  • Be responsible for compliance-related deliverables, including audit support, observation response, presentations to sr. management and site leadership, and generating trend reports.
  • Support compliance culture initiatives and assist in implementing changes.
  • Develop the team through the creation and delivery of proactive and reactive trainings.
  • Assist with developing tools and resources to improve the investigative process.
  • Support Scientist I investigators when needed.
  • Average 3-4 deviation/OOS/CAPA record closures per month.
  • Complete overdue assessments and file record extensions as required.
  • Author and revise SOPs as needed.
  • Assist with formulating continuous improvement strategies and timelines.
  • Perform other job duties as assigned., Biology Research Chemistry Visionary Leadership Innovation Stage Gate Problem Solving Materials Science Influencing Skills Feasibility Studies Technology Scouting Scientific Literature Intellectual Curiosity New Product Development Artificial Intelligence Engineering Design Process Fast Moving Consumer Goods Verbal Communication Skills Influencing Without Authority +0 Quality Manager - Fenton, MO Hubbell Fenton, MO*On-Site Auditing Leadership Innovation Resilience Coordinating Data Centers Data Collection Vertical Market Quality Assurance Project Management Quality Management Telecommunications Capability Assessment Quality Certification Training And Development Balancing (Ledger/Billing) Ethical Standards And Conduct +0

Google IT Automation with Python Mid-Level SQL Engineer Leidos Saint Louis, MO*On-Site MySQL Linux CI/CD Grafana Equities Dashboard Operations Innovation PostgreSQL Market Data Window Function Ancient History Computer Science Agile Methodology Software Engineering Analytical Dashboard Relational Databases SQL (Programming Language) Tableau (Business Intelligence Software) Top Secret-Sensitive Compartmented Information (TS/SCI Clearance) +0

Google IT Automation with Python

Requirements

Visionary Leadership Management Innovation Osmolality Biochemistry Communication Presentations Investigation Pharmaceuticals Microsoft Excel Safety Assurance Active Listening Biochemical Assays Analytical Chemistry Artificial Intelligence Engineering Design Process Good Manufacturing Practices Continuous Improvement Process Good Laboratory Practice (GLP) Corrective And Preventive Action (CAPA), * Experience in GMP, Chemistry, Analytical Chemistry, QC, and Quality Control.

  • HPLC pharmaceutical QC experience.
  • Compendial Testing (pH, UV, Osmolality, Appearance).
  • OOS/OOT investigations., * Bachelor's degree in a science-related field with 3-4 years of industry experience.
  • Experience in a Pharmaceutical FDA/GMP regulated environment and working in a QC position.
  • Experience with any bio-assay or biochemistry assays is a plus.
  • TrackWise and TapRooT experience is a plus but not required.
  • Knowledge of GMP regulations, GLP, and GDP.
  • Proficient in standard computer programs such as SmartSheet, PowerBI, MS Excel, Word, and PowerPoint.
  • Strong communication skills, including active listening, facilitation, and escalation.
  • Ability to inspire innovation and team effectiveness.

Benefits & conditions

The position will be all onsite for training, with the option to work one day from home once trained. It requires wearing gloves and other PPE to enter laboratory spaces. The role involves extended periods of desk time and meetings. The team comprises four members and a supervisor, with an onboarding period of 3-6 months. Job Type & Location

This is a Contract to Hire position based out of Berkeley, MO. Pay and Benefits

The pay range for this position is $32.00 - $38.46/hr.

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) Workplace Type

About the company

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.

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