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Senior Associate Quality Control General Chemistry (JP7169)

West Greenwich, Rhode Island · Biotech/Pharmaceutical
Job Title: Senior Associate Quality Control General Chemistry (JP7169)
Location: 40 Technology Way, West Greenwich, Rhode Island 02817
Employment Type: Contract
Duration: 12 months with likely extensions.
 
3 Key Consulting is hiring a Senior Associate Quality Control General Chemistry for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
 
Job Summary:
  • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks.
  • Operate and maintain specialized laboratory equipment and instrumentation.
  • Participate in laboratory investigations and audits as necessary.
  • At all times, comply with safety guidelines, cGMPs and other applicable regulatory requirements.
  • Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with cGMP practices and other applicable regulations.
  • Performs review and approval of procedures, assays, documents and records, including but not limited to Nonconformance records and CAPAs.
  • Supports Continual Improvement initiatives, programs and projects.
  • Alerts management of quality, compliance, supply and safety risks.
  • Supports internal/external audits and inspections.
  • Completes assigned training to permit execution of tasks.
  • Performs additional duties as specified by management.
 
Basic Qualifications:
Master's Degree OR Bachelor's Degree and 2 years of Quality or Analytical Laboratory experience OR Associate's degree and 6 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 8 years of Quality or Analytical Laboratory experience.
 
Top Must have Skill Sets:
  • 2 years of general chemistry experience.
  • Experience in General chemistry analysis such as pH, Osmolality, Subvisible particles, Visual inspection, and UV. 
    Demonstrated experience in investigations, change control, validation, audits, QC processes.
  • Demonstrated ability to interpret scientific literature.
  • GMP/GDP experience.
  • Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision.
  • Strong communication skills (both written and oral), facilitation and presentation skills.
 
Employee Value Proposition:
Quality Control Laboratories are a fast-paced organization with opportunities to cross-train on several analytical assays. We are a motivated, high performing team in close proximity to manufacturing, so the candidate will get a holistic view of the drug manufacturing process.
 
Red Flags:
No PhD candidates as this is a more entry level position.
 
Interview Process:
 Manager will do a phone screen and then if they are a good candidate we will arrange a skype interview.
  
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
 
 
 
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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