Planet Pharma · 1 day ago
Quality Control Associate
West Greenwich, RI
Contract
Onsite
Entry Level
1+ years expPlanet Pharma is seeking Quality Control Associates for a 1-year+ contract to support routine GMP analytical testing. The role involves performing various analytical tests and ensuring compliance with safety guidelines and GMP practices.
BiotechnologyHealth CarePharmaceutical
No H1B
Hiring Manager
Amanda Thaxton
Responsibilities
Performing analytical testing including time sensitive samples from Manufacturing (Titer/ MMV/ Mycoplasma/ Endotoxin/ Bioburden/ TOC/ Conductivity), Centralized Raw Material testing (compendial testing & microbiology), Environmental Monitoring and Critical Utilities, Sample Receipt and Aliquot
Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with safety guidelines, cGMP (Good Manufacturing Practices) practices and other applicable regulations
Generates complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
Operates laboratory equipment and instrumentation
Performs review and approval of assays, documents and records
Supports troubleshooting and problem solving
Alerts management of quality, compliance, supply and safety risks
Supports TRAs and deviations, as applicable
Completes required assigned training to permit execution of required tasks
Performs additional duties as specified by management
Qualification
Required
4 JOB OPENINGS: QC Associates needed for a 1‑year+ contract in West Greenwich, RI (Onsite) to support routine GMP analytical testing on night shifts (Tuesday-Friday from 9:45pm - 8:15am)
Ideal candidates have a science degree with experience in HPLC, microbiology, and GMP lab practices
This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing
The ideal candidate enjoys tackling challenges and excels at time management with attention to detail
Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy
Demonstrated ability to work independently and deliver right first time results
Excellent communication skills (written and verbal)
Must have focus on data integrity
Qualified to work in the U.S. without employer sponsorship
Commitment of a 40-hour work week (4 x 10hr shifts) in West Greenwich, RI
Requires Experience: Bachelors degree OR Associate's degree and 1-2 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 3 years of Quality or Analytical Laboratory experience
Preferred
1-3 years of experience in GMP analytical laboratory
Experience executing analytical /biological testing per Methods and/or Compendia
Experience with QC analytical systems and/or Quality systems
Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision
Strong communication skills (both written and verbal)
Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories
Understanding of biopharmaceuticals process and related unit operations
Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
Independent, self-motivated, organized, able to multi-task in time-sensitive environments
Demonstrated experience in investigations and QC processes
Company
Planet Pharma
Planet Pharma is a pharmaceuticals company.
1001-5000 employees
Funding
Current Stage
Late StageLeadership Team
Cynthia Lewis
Senior Executive Recruiter, Life Sciences - PPG Advisory Partners
Emma Morris
President, PPG Advisory Partners
Company data provided by crunchbase