Associate Quality Control Lab
aditi consultingWest Greenwich, RI
$32.00 - $35.00/hrAPPLY NOW (opens in a new tab)
Associate Quality Control Lab
aditi consultingWest Greenwich, RI
today
Industries
Pharmaceutical Preparation ManufacturingResearch and Development in BiotechnologyBiological Product Manufacturing$32.00 - $35.00/hr
APPLY NOW (opens in a new tab)About the role
Payrate: $32.00 - $35.00/hr.
Summary:
This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
Responsibilities:
Performing analytical testing including time sensitive samples from Manufacturing (Titer/ MMV/ Mycoplasma/ Endotoxin/ Bioburden/ TOC/ Conductivity), Centralized Raw Material testing (compendial testing & microbiology), Protein Concentration via UV/VIS and HPLC, 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
Qualifications: Bachelor’s 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 Qualifications: 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
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
Top 3 Must Have Skill Sets:
Ability to work in a fast paced, GMP environment
Familiarity with Quality ideology (GDP, GMP, etc.)
Technical skill in wet chemistry, HPLC, microbiology, USP/EP testing
Pay Transparency:
The typical base pay for this role across the U.S. is: $32.00 - $35.00/hr. 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, dental, and vision 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.
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JOB OVERVIEW
Salary
$32.00 - $35.00/hr
Experience level
Junior
Location
West Greenwich, RI
Occupation
Quality Control Analysts
Industry
Pharmaceutical Preparation Manufacturing
Posted
today
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