Job Description
Job Title - CQ Lab Analyst
Our client in Rocky Mount is looking for hardworking, motivated talent to join their team. Be able to work at a Fortune 100 company and make a difference. Don't wait… apply today!
What's in it for you?
* Onsite is a must for this position
* Contract or Permanent - This is a contract position
* Full time hours
Job Description
This position is specific to Incoming Material testing. All applicants must be able to interpret commodity specification instructions while adhering to all local laboratory policies and SOPs. Applicants should be comfortable with dynamic work sequences and must be self-motivated and work with minimal direction
ROLE RESPONSIBILITIES
* 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.
* Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals.
* When faced with roadblocks and issues, routinely offers suggestions for improvements
BASIC QUALIFICATIONS
* 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
* Medical, Dental, Vision, 401k
* Weekly pay with direct deposit
* Consultant Care support
* Free Training to upgrade your skills
* Dedicated Career Partner to help you achieve your career goals
Are you Interested?
Share this job with friends and family and earn dollars with every successful hire.