IPQA Operators

Largo, FL

Posted: 09/10/2019 Job Number: JN -092019-11106
IPQA Operators

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Title: IPQA (In-Process Quality Assurance) Operators
Location: Largo/Clearwater Area, Florida
Industry: Pharmaceutical and Chemical Manufacturing
Shifts Available: All shifts M-F; 1st, 2nd and 3rd currently, but could move to 12- hour shift in beginning of 2020. 1st shift 7am-3:30pm, 2nd shift 3pm-11:30pm and 3rd shift 11pm-7:30pm (must be willing to work over-time including weekends)
Salary: Up to $17.50/hour, plus shift differential accordingly
Employment Type: Direct hire

Environment: This client innovates, formulates and manufactures pharmaceutical brands. They serve companies in pharmaceutical, cosmetic, personal care and chemical applications. Using state-of-the-art equipment, their team of experts work to ensure high quality. Highly differentiated products are brought to market with exceptional customer service. Isn t this the type of company you want to work for?

MAJOR DUTIES AND RESPONSIBILITIES:
  • Adherence to all company procedures/SOPs (Standard Operating Procedures)
  • Demonstrates Good Documentation Practices (GDP)/Good Manufacturing Practices (cGMP) daily
  • Responsible for in-process testing. Responsible to take samples from the line as it is produced; visual inspection, measuring and ensuring proper labeling/bundling.
  • Performs finished product inspections on all the products using measuring gauges (calipers, crimp gauges, pressure gauges, etc.); scales; visual inspection
  • Performs review of in-process checks
  • Verifies pre and post clearance activities during production runs.
  • Performs daily verification of instrumentation (scales, gauges, etc.)
  • Performs monitoring and verification of monthly logbooks (temperature, pressure differential, equipment logs, etc.)
  • Accurately reviews and records data.
  • Accurately collects retain samples and samples for Analytical and Micro Lab
  • Performs audits of the batch records
  • Acts as a liaison between Quality and Production
  • Demonstrates proficiency in quality finished product inspections on at least 75% of different production machine lines
  • Provides support to all other departments in an overall quality capacity when needed (lab, warehouse, etc.)
  • Promotes continuous improvement and customer satisfaction
  • Participates in other activities as required by Quality Management

QUALIFICATIONS:
  • Working knowledge of FDA regulations for pharmaceuticals and/or medical devices.
  • Knowledge of inspecting critical parameters for following products: aerosols, tubes, liquids
  • Minimum High School diploma or equivalent
  • No matter what shift, training will be done on 1st shift (7am-3:30pm, M-F) up to 8 weeks. One must be available for this schedule.
  • Identify root cause of problem, document and solve
  • Ability to use a personal computer and measuring devices
  • Attentive to detail, thorough and accurate and quick decisions
  • Ability to establish priorities, work independently, productively, and proceed with objectives without supervision.
  • Ability to work in a fast paced environment sometimes rapidly shifting priorities. Ability to concentrate in such an environment and perform quality work.

EOE/ADA
Search words: IPQA, inspections, in-process, manufacturing, FDA, QC, Quality Control, root cause, documentation, samples

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