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CQ Lab Analyst II
Ref No.: 19-00031
Location: Rocky Mount, North Carolina
Position Type:Contract
Start Date / End Date: 01/17/2019 to 01/17/2020
The CQ Lab Analyst II, will perform basic analysis for raw materials, in process and finished products a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality.
Report testing results through computerized systems, or through standard laboratory paper-based documentation.  Other related duties essential to these operations or special assignments as required.
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
Must be self-motivated and work with minimal direction
Demonstrate proficiency in computerized systems (Experience and use of LIMS, Empower are plus).
Demonstrated ability to troubleshoot analytical methods
Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve RFT and schedule adherence as needed
Works with supervision and management to identify opportunities to improve testing efficiencies
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 and actively participates in associated improvement activities wherever possible
Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift and across shifts wherever possible.
Maintains an on-time training
Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter as wells as more advanced techniques, i.e. GC, HPLC, AA, FTIR, etc.
BS/MS in Chemistry or BS Science Degree
At least 2 years analytical laboratory experience in a GMP regulated environment.
Experience in parenteral drug product pharmaceutical manufacturing is plus.
Successful hands-on analytical testing experience in a GMP environment.
Stand up for up to 8 hours, sit for up to 8 hours, walking, climbing stairs, responding to visual warning indicators, respond to audible warning indicators, respond to color or special visual indicators, wear specialized protective clothing (lab coat, safety glasses, gloves, face shield/goggles, apron), repetitive use of upper extremities.
There are no out of the ordinary travel or shift requirements associated with the position.   Individual will be expected to work nonstandard schedule as needed to support the business objectives
Senior Leader
Global Job Level J120+ (Vice President, US Grades 21+) Manager
All roles Global Job Level  J090+ (Sr. Manager-Sr. Director);  and People (Colleague) Manager roles J060+ (Sr. Associate/Scientist US Grades 7-20)
Anticipates Customer & Market Needs  
Grows Leaders
Demonstrates Business Acumen
Leads Change
Strategic & Innovative Thinking
Builds Change Agile Organizations           
Acts Decisively
Acts Decisively
Seizes Accountability
Commits to "One Pharmaceutical”
Seizes Accountability
Insight, Influence & Inclusion
Holds People Accountable
Builds Effective Teams
Holds People Accountable
Commits to "One Pharmaceutical”
Grows Others