QC Chemist II

QC Chemist IIThe QC Chemist II position performs testing using a variety of analytical techniques. The successful candidate ensures that testing and documentation is compliant with GMP regulations and internal procedures. The position will be operating within a GMP environment for an Analytical QC team in a CDMO. Essential functions include:Well versed with various laboratory techniques, including, but not limited to HPLC, GC, titrations, and various wet chemistry techniques.Carry out routine laboratory work as directed by management and/or senior laboratory personnel with minimal supervision.Performs complex analyses with moderate supervision.Conduct routine analytical experiments using established analytical methods and procedures.Data entry into reports, as directed by senior laboratory personnel.Verify simple transcription processes, such as checking accuracy of calculations and reviewing daily equipment verifications for compliance.Support testing for investigations for OOS, OOT, and aberrant results and troubleshooting.Review and maintain laboratory notebooks.Ensure data collected is processed and submitted for review in a timely manner.Aid in investigations for OOS, OOT, and aberrant results and troubleshooting by assisting in root cause determination and report writing.Maintains laboratory inventory of chemicals, standards, and consumables and orders materials as necessary.Revises existing methods, SOPs, and Work Instructions as needed.Supervisory responsibilities:Direct Reports: NoneIndirect Reports: NoneKey relationships:Manufacturing OperationsAnalytical R&DQuality AssuranceTravel requirements:N/AEducation and experience:B.S with 4-6 years' experience, or M.S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline2-5 years’ experience in a GMP laboratory setting in the pharmaceutical industryMust have experience with general laboratory instruments, such as FTIR, Particle Size, Titration Equipment, and UV-VisMust have experience in HPLC testing and troubleshootingMust have prior experience with raw materials or finished products testing in a GMP pharmaceutical environment.Must be well versed with Good Documentation Practices and ALCOA++ principles.Technical report writing proficiency preferredKnowledge, skills, and abilities:Proficiency in Empower, MS Excel, and MS WordSpeaks, writes, listens and presents information in a logical and articulate manner appropriate for the audienceThorough when performing work, conscientious about attending to detail, and uses logical thinking that is well-organized and methodical and has a right first-time mentalityPhysical demands and work environment while performing the duties of this job, there may be certain physical demands required for the position:Requires constant standing, walking, seeing, gripping, & hearingRequires frequent sitting, bending, pushing, & reachingRequires occasional carrying under 20 LBS.Requires frequent lifting & pulling under 20 LBS, occasionally 20 – 60 LBS.Requires occasional twistingOther duties you may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Limitations and disclaimer the above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.