CQ Lab Analyst

  • location: Rocky Mount, NC
  • type: Contract
  • salary: $30.44 - $35.81 per hour
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job description

CQ Lab Analyst

job summary:
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location: Rocky Mount, North Carolina
job type: Contract
salary: $30.44 - 35.81 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
Job Responsibilities

To support the R3 method remediation project at the Rocky Mount NC manufacturing site.

Under direction of the Chemical Quality group, according to project schedule:

- Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.

- Follows procedures at all times, adopting cGMP, cGDP practices.

- Follows supervisor directions at all times.

- Able to function independently, but asks questions as necessary

- Accepts dynamic work sequences

- Actively participates in daily and weekly planning discussions with his/ her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed

- Consistently communicates work sequence status to supervisor in a timely manner.

- Where scheduled work was not achieve d, actively participates in discussions to identify opportunities for correction and improvement.

- Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals.

- When faced with roadblocks and issues, routinely offers suggestions for improvements

 
qualifications:
Education & Qualifications

BS/MS in Chemistry or BS Science Degree, 0-2 years experience.

** QC experience HUGE plus!

- Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift wherever possible.

- Has understanding of basic non-instrumental and instrumental techniques including, but not limited to: wet chemistry techniques, Manual Titrations , pH, Conductivity, Autotitrations, UV­ Vis, Polarimeter, HPLC

- Willing to learn and develop a career in the pharmaceutical industry.

- Capable to read, understand, and execute instructions in basic laboratory procedures.

- Experience in parenteral drug product pharmaceutical manufacturing is plus but not required.

- Successful hands-on analytical testing experience in a GMP environment is plus

 
skills: Quality control, Chemistry, GMP (Good Manufacturing Practice)
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.

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