Job Description

Pancap Pharma Inc. is a leader in specialty contract manufacturing of pharmaceutical dosage forms. The company began its contract manufacturing operations in January of 1994 and since then has translated experience into quality production for a wide range of clients.

From concept to full package delivery, we have the experience and commitment to meet the needs of even the most unique clients. We offer a wide range of manufacturing and support capabilities including capsule fabrication, compounding of non-sterile liquids, packaging, labelling, regulatory affairs, testing and quality assurance. The products we manufacture are then shipped around the world. Quality is the cornerstone upon which Pancap has built its foundation. Our Quality Assurance System was developed in order to ensure the production of safe and effective products in compliance with the current Good Manufacturing Practice (cGMP) regulations, industry standards and our client's specifications/marketing requirements.

We are growing our operations with in

Markham, Ontario

and we are looking for a QC Analyst Position

GENERAL REQUIRMENTS:

Respects and adheres to company polices at all the time Perform all work in accordance with cGMP and approved procedures to ensure the technical integrity and regulatory compliance of all data generated. Checks results for accuracy and ensure compliance to cGMP/GLP and SOP's Good understanding of test procedures and basic analytical principles Able to operate laboratory instrumentation with minimum guidance, such as: Karl Fisher, UV/IR Spectrophotometers, Dissolution apparatus, Viscometer, Polarimeter, TOC, GC, pH Meter, Conductivity meter, 718 STAT Titrino. Identifies simple technical problems related to instruments operation, and solves as necessary Identifies preventable errors prior to the start or completion of the test and report as appropriate Applies the knowledge gained previously in the lab to improve the quantity and quality of work. Organizes work efficiently and utilizes time efficiently. Able to perform multitask. Completes documentation as soon as testing is done and review data for completion and accuracy Recognize and report OOS/OOT results to Supervisor in a timely manner (upon completion of testing) Issues of OVR/MVR/OOS as needed Performs validation of test methods and production processes Takes the responsibility and accountability for the duties assigned Able to work independently and within a team environment. Actively participate in team related tasks. Support the team on meeting deadlines Participate in on-going training as required Ability to work shift when required Communicates to Supervisor/or Designate any potential delay for the projects assigned

MAJOR DAILY ACTIVITIES:

Sample and test all Raw Materials according to current SOP and within GMP compliance Monitoring of Airflow patterns and pressures in Production Areas Calibration of Test Equipment Environmental Microbial Sampling Inspection and testing of In-Process material and packed Finished Products Testing and results evaluation of Stability Product Sampling and Testing of Packaging Components Monitoring temperatures throughout the Plant Weekly water testing utilizing TOC and Conductivity meter Perform other duties as assigned Adhered to Health and Safety policy
Job Type: Full-time

Pay: $22.00-$24.00 per hour

Expected hours: 36 - 40 per week

Work Location: In person