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Analytical Chemist Ii /Bio-Chemist

Company

ASCENDING

Address , Chantilly, Va
Employment type FULL_TIME
Salary
Expires 2023-06-26
Posted at 1 year ago
Job Description

Job Type

Full-time

Description

**Multiple positions available in QC and R&D**


Job Summary:

The role of QC Biochemist/Analytical Chemist II is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing raw materials, in-process, finished formulations, stability samples, method development and/or transfers, and cleaning validations. Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity, and timing. Responsible for the safe and efficient execution of job duties.


JOB DUTIES & RESPONSIBILITIES:

  • Perform the Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, UV spectrophotometer, Dissolution apparatus, KF Auto titrator, FT-IRS spectrophotometer, Polarimeter and Refractometer.
  • Participate in out-of-specification and failure investigations. Support all aspects of laboratory investigations.
  • Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished product release and stability using approved methods and various instrumentation while adhering to cGMP and established policies.
  • Prepare, review and approve analytical data, technical reports and analytical methods.
  • Coordinate Microbiological, preservative efficacy/ antimicrobial effectiveness testing requirement as per USP/USP-NF for Active pharmaceutical ingredients, Inactive and Finished products and stability samples for regulatory filings.
  • Conduct analytical USP method verifications, validations, and method transfer activities for raw materials and finished dosage forms.
  • Interpret test results, compare them to established specifications and control limits, and ensure appropriateness of data for release. Treats data with a high level of integrity and ethics.
  • Compile laboratory test data and perform appropriate analyses that include physical (solubility, viscosity),chemical (titration) and analytical (FTIR, HPLC, ICP-MS, UV-Vis, KF, IC) testing etc.
  • Complete documentation needed to support testing procedures including test forms and logbooks.


Physical Requirements/Working Environment:

  • Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.
  • Commitment to long hours of work when necessary to achieve goals.
  • Respirator, lab coat and safety glasses required. Ability to work with potent substances using a glove-box.

Job Type: Full-time

This Job Is Ideal for Someone Who Is:

  • Autonomous/Independent - enjoys working with little direction
  • Achievement-oriented - enjoys taking on challenges, even if they might fail
  • High stress tolerance - thrives in a high-pressure environment
  • Adaptable/flexible - enjoys doing work that requires frequent shifts in direction
  • Innovative - prefers working in unconventional ways or on tasks that require creativity
  • Detail-oriented - would rather focus on the details of work than the bigger picture
  • People-oriented - enjoys interacting with people and working on group projects
  • Dependable - more reliable than spontaneous


Requirements

Preferred Knowledge & Skills:

  • Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
  • Solid knowledge of FDA/ICH regulations.

Required Experience & Education:

  • Minimum 1 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.
  • BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.

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