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- 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 achieved, actively participates in discussions to identify opportunities for correction and improvement.
- Applicant must have a High School Diploma (or Equivalent) and 4 years of relevant experience OR an associates degree with 2 years of experience OR a bachelors degree with 0+ years of experience.
- Certification in assigned area, if applicable
- 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
- 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 achieved, 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
- 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 wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis,Polarimeter, etc.
- Has understanding of performing basic measurements on packaging materials using various instruments including optical comparators, Vernier calipers, gauges, etc.
- Demonstrate proficiency in computerized systems, such as Laboratory Information Management System
- Incoming Materials experience preferred
- ID: #49900683
- State: North Carolina Rockymount 27803 Rockymount USA
- City: Rockymount
- Salary: USD TBD TBD
- Job type: Contract
- Showed: 2023-05-10
- Deadline: 2023-07-08
- Category: Et cetera