Quality Control Analytical Associate II

1 week ago

Saddle Brook, United States Lynkx Staffing LLC Full time
Job DescriptionJob DescriptionQuality Control Analytical Associate IIAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT & Human Resources disciplines in New Jersey. The Quality Control Analytical Associate II serves as a support role to clinical and commercial production. The QC Analytical Associate II will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. Under the direction of the Manager, QC Analytical Associate II, responsibilities include:
  • Performs the accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populations
  • Performs maintenance, monitoring, and troubleshooting of pertinent equipment
  • Performs and assists in the training of other Quality Control technicians
  • Maintains training records and coordinates records retention with Document Control and Training groups
  • Tests, documents, and reports results for products or materials following company and/or client procedures following CGMP and/or GTP guidelines
  • Performs state proficiency testing and/or client proficiency testing under direct supervision as applicable
  • Participates in managing QC materials and supplies
  • Performs and assists in equipment and method qualification/validation activities as needed
  • Performs reagent and media preparation
  • Provides input based on level of knowledge and experience with troubleshooting malfunctioning equipment
  • Investigates out-of-specification, out-of-trend, aberrant, and/or non-conforming test results
  • Initiates, investigates, and prepares deviation reports with input from assigned supervisor
  • Brainstorms and implements corrective and preventive actions, as and when applicable
  • Documents training and execution of shipping test samples to contract laboratories for testing
  • Completes all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
  • Communicates effectively with other co-workers, departments, management and clients
  • Eventually serves as a lead and/or co-lead for client projects
  • Additional tasks as assigned
REQUIREMENTS
  • BA/BS in a science or relevant field required
  • Prior cGMP experience required
  • Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a CGMP/GTP environment preferred
  • Prior industrial experience in cell count methodologies preferred
  • Prior academic and/or industrial cell therapeutic experience preferred
  • Minimum 2-5 years of experience in Quality Control laboratory setting or within the biopharmaceutical industry
  • Proficient with computer software such as: Microsoft Office, Visio
  • Strong written and oral communication skills
  • Strong presentational skills preferred
  • Candidate must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities.
Other Information
  • While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.
  • Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy. Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays, and as required by the company
  • Must be able to handle the standard/moderate noise of the manufacturing facility
  • The QC Analytical Associate II must be able to work in a laboratory environment for an extended period.
  • Must be physically capable to stand; walk; sit; bend; stretch; use hands to finger, handle or feel; reach with hands and arms; and talk or hear
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. QC Analytical Associate I is available as well.

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