Associate Scientist

Aditi Consulting

Thousand Oaks, CA

JOB DETAILS
SALARY
$24–$25 Per Hour
SKILLS
Analysis Skills, Artificial Intelligence (AI), Artificial Intelligence (AI) Programming Languages, Asepsis, Automotive Automation, Biochemistry, Biomedical Engineering, Biotech and Pharmaceutical, Chemical Engineering, Chemistry, Clinical Support, Computer Networks, Consulting, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Analysis, Drug Design, Drug Development, Drug Products, Experiment Design, Failure Mode and Effects Analysis (FMEA), GMP (Good Manufacturing Practices), Gap Analysis, Identify Issues, Investigational New Drug (IND), Laboratory Notebook, Manufacturing, Manufacturing Operations, Manufacturing Requirements, Manufacturing Technology, Marketing Software, Messaging Technology, Modeling Languages, Performance Analysis, Performance Modeling, Pilot Plant, Presentation/Verbal Skills, Problem Solving Skills, Process Development, Process Improvement, Process Manufacturing, Process Modeling, Product Design, Project/Program Management, Purchasing/Procurement, Quality Assurance Methodology, Record Keeping, Regulations, Regulatory Compliance, Regulatory Submissions, Risk Analysis, Root Cause Analysis, Scientific Principles, Short Messaging Service (SMS), Speech Technology, State Laws and Regulations, Statistical Analysis System (SAS), Statistics, Statistics Software, Strategic Planning, Telephony, Test Plan/Schedule, Testing, United States Department of Energy (DOE), Writing Skills
LOCATION
Thousand Oaks, CA
POSTED
16 days ago
Payrate: $24.00- $25.00/hr.
 
Summary:
As a member of the process development team, this role will be focused on identifying and developing aspects of drug products to advance process design for parenteral drug products. The candidate will perform experiments, organize data and analyze results with minimal supervision. The candidate will establish experimental design, develop and implement protocols, obtain reproducible and reliable results, analyze data and communicate results to cross functional groups.
 
Responsibilities:
  • Design, execute and document primary data packages related to drug product design and process development, and communicate key findings in presentations
  • Develop solutions to technical problems during process characterization and aseptic manufacturing
  • Support one or more clinical and commercial process introductions or process transfers into manufacturing network
  • Author and review technical protocols, reports, product impact assessments, and regulatory sections in support of IND and marketing application submissions
  • Provide ongoing support to clinical and commercial fill/finish manufacturing operations through troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements
  • Participate in cross-functional teams working effectively in a highly matrixed team environment to drive change, efficiency, and strong relationships
 
Requirements:
  • BS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology with 3+ years of experience within the pharmaceutical/biotechnology industry
  • MS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology
  • Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters
  • Aseptic fill finish manufacturing or manufacturing technical services experience including the development of control strategies and active process performance monitoring
  • Understanding process related stresses that impact the quality and stability of biologics
  • Ability to use engineering principles to leverage bench and pilot scale models for process performance characterization
  • Fill/finish process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools (e.g. Fish bone diagrams, FMEA, etc.)
  • Familiarity with Design of Experiments (DOE) and Quality by Design (QbD) principles
  • Familiarity with cGMPs, regulatory filings, and compliance issues for sterile injectable products manufactured by aseptic processing
  • Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality
  • Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions
  • Ability to learn and act on dynamic information at a rapid pace
  • Familiar or ability to learn to use electronic record keeping, GMP, laboratory notebooks, statistical analysis and software.
  • Laboratory or pilot plant experience with process equipment
 
Must Have Skills:
  • Aseptic fill finish manufacturing or manufacturing technical services experience including the development of control strategies and active process performance monitoring
  • Ability to use scientific principles to leverage bench and pilot scale models for process performance characterization
  • Fill/finish process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools (e.g. Fish bone diagrams, FMEA, etc.)
  • Perform data analysis using advanced statistical/analytical techniques with a proficiency in statistical analysis software.
  • Nice to have: Leverage advanced AI technologies, including generative AI, large language models (LLMs), and in silico modeling, to drive innovation and accelerate research, development, and testing processes.
  • Perform data analysis using advanced statistical/analytical techniques with a proficiency in statistical analysis software.
 
Pay Transparency: The typical base pay for this role across the U.S. is: $24.00- $25.00/hour. Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, denmatch, lifeion benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match,  life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law. 
 
Consent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary.
You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts. You also acknowledge and agree to Aditi Consulting LLC’s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions. Calls may be recorded.
 
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Aditi Consulting