What are the responsibilities and job description for the Quality Control Senior Associate position at Randstad Life Sciences US?
Job Summary
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: $20 - 24 per hour
work hours: 9 to 5
education: Bachelors
Responsibilities
Required
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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
u50000030026
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: $20 - 24 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.
Required
- Bachelor's degree and 1-2 years of Quality or Laboratory experience
- General Chemistry/HPLC/Capillary Electrophoresis experience in a GMP setting
- Quality Control experience in a GMP setting
- Experience in GMP analytical laboratory
- Experience with HPLC/UPLC, general chemistry, capillary electrophoresis
- Empower and LIMS knowledge.
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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
u50000030026
Salary : $20 - $24
