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Quality Control Analyst

The Staffing Resource Group, Inc

Quakertown, PA

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JOB DETAILS
SALARY
SKILLS
Analysis Skills, Analytical Method Validation, Application Programming Interface (API), Biotech and Pharmaceutical, Communication Skills, Computer Skills, Continuous Improvement, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Data Quality, Documentation, Equipment Maintenance/Repair, FDA (Food and Drug Administration), GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Housekeeping/Cleaning, Leading Edge Technology, Lift/Move 30 Pounds, Manufacturing, Materials Testing, Metrics, Multitasking, Presentation/Verbal Skills, Product Support, Quality Control, Quality Management, Record Keeping, Regulatory Requirements, Safety Process, Safety/Work Safety, Team Player, Technical Support, Testing, Time Management, Training/Teaching, Writing Skills
LOCATION
Quakertown, PA
POSTED
30+ days ago
Quality Control Analyst

Title: Quality Control (QC) Analyst
Location: Quakertown, PA
Industry: Pharmaceutical
Salary: $25/hr. + 10% Shift Differential
Schedule: Training Hours will be 1:30pm-11:30pm, Mon-Thurs. After training period of 60-90 days, QC Analyst will then work from 4:30pm-2:30am, Mon-Thurs.
Employment Type: Direct Hire

Company Overview:
Operating from a 100,000 square foot, US-based, state-of-the-art, FDA inspected facility, this company has the experience and capabilities to rapidly develop, scale up, and process APIs and excipients ranging from grams to multi-metric tons, including highly potent compounds.

Job Overview:

The Quality Control Analyst is critical to the Company s success in providing a quality service to our customers in a timely fashion. This position carries out the practical work in the laboratory such as routine analytical testing. Performs required testing on raw materials, intermediates and finished products. May support Quality management to provide method technology transfer and project preparation. Follows GLP and cGMP procedures and documenting actions.

Job Description:
  • Testing of raw materials, intermediates and finished products
  • Records test results and maintains raw data and accurate laboratory records
  • Maintain lab assets in accordance with written procedures & regulatory requirements
  • Approve or reject finished product samples
  • General lab support including housekeeping, equipment maintenance, inventory of supplies, etc.
  • Runs analytical method transfer and validation experiments.
  • Assist on preparation work of projects
  • Assist on the OOS investigations
  • Provide technical support and answers during the analysis of production sample
  • Assist with various duties when needed as instructed by supervisor
Education:
  • Associates degree or higher
  • GMP or Quality experience preferred
  • HPLC experience preferred
  • Microtrac (Particle Size) preferred
  • Basic computer skills
  • Strong communication skills both verbal and written required
Essential Job Functions:
  • Must understand and follow job safety procedures at all times
  • Adherence to cGMPs is required at all times.
  • Majority of role is laboratory based and must abide by good laboratory practices.
  • Wear PPE as required.
  • Must accurately record process details.
  • Ability to multi-task in a fast-paced manufacturing environment.
  • Must be able to lift 30lbs
Why Join Us
  • Consistent weekday schedule with paid breaks & opportunities for overtime
  • Gain hands-on experience with cutting-edge pharmaceutical technologies
  • Work in a facility trusted by top pharmaceutical and biotech companies worldwide
  • Great entry point into the pharmaceutical industry
  • Join a collaborative team where safety, quality, and continuous improvement come first
EOE/ADA
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About the Company

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The Staffing Resource Group, Inc