- Under general supervision, this position will perform routine procedures to support drug substance and drug product testing within Quality Control.
- Tasks may include but are not limited to performing sample collection, sample handling, testing equipment/laboratory support.
location: West Greenwich, Rhode Island
job type: Contract
salary: $35.00 - 43.64 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Performing routine laboratory procedures
- Documenting, computing, compiling, interpreting, and entering data into computerized systems
- Maintaining and operating specialized equipment
- Initiating and /or implementing changes in controlled documents.
- Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks.
qualifications:
- Master's degree OR Bachelors degree and 1-2 years of Quality or Analytical Laboratory experience OR Associate's degree and 3-5 years of Quality or Analytical Laboratory experience OR High school diploma/GED and +5 years of Quality or Analytical Laboratory experience.
- Experience in GMP analytical laboratory
- Experience with HPLC/UPLC, general chemistry, capillary electrophoresis
- Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
- Must have focus on data integrity
- Qualified to work in the U.S. without employer sponsorship
- Ability to work independently and deliver right first time results
- Excellent communication skills (written and verbal)
- 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
- Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.
- Understanding of biopharmaceuticals process and related unit operations
skills: Quality control, Chemistry, GMP (Good Manufacturing Practice), High Pressure Liquid Chromatography (HPLC), Good Manufacturing Practices (GMP), Quality Control (QC)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
