About Pancap Pharma Inc.
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, labeling, 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.
Join Our Team
We are growing our operations with a brand-new state of the art facility in Windsor, Ontario and we are looking for a contract QC Laboratory Supervisor.
Role and Key Responsibilities
QC Supervisor - Windsor
Responsibilities:
1. Always respects and adheres to company policies.
2. Adhere to Health and Safety Policy.
3. Perform all work in accordance with cGMP and approved procedures to ensure the technical integrity and regulatory compliance of all data generated.
4. Check results for accuracy and ensure compliance to cGMP/GLP and SOP’s.
5. Good understanding of test procedures and basic analytical principals.
6. Able to operate laboratory instrumentation such as: UV/IR Spectrophotometers, Dissolution Apparatus, TOC, pH Meter, Conductivity Meter, Auto-Titrator.
7. Identifies simple technical problems related to instruments operation and solves as necessary.
8. Identifies preventable errors prior to the start or completion of the test and report as appropriate.
9. Applies the knowledge gained previously in the lab to improve the quantity and quality of work.
10. Organizes work efficiently and utilizes time efficiently.
11. Completes documentation as soon as testing is done and review data for completion and accuracy prior to handing in for review.
12. Recognize and report OOS/OOT results in a timely manner.
13. Issue Non-Conformance/Non-Impact Notices/OOS/OAL or Change Request as needed.
14. Schedule/perform validation and transfer of test methods and production processes.
15. Takes responsibility and accountability for the duties assigned.
... (more responsibilities listed)
Qualifications and Experience
Requirements:
* University Degree or College Diploma in a science-related field.
* 3 years Quality Control experience preferred.
* Experience in a pharmaceutical laboratory environment preferred.
* Good knowledge of laboratory GMP and demonstrated proficiency in analytical techniques.
* Works well in a fast-paced environment both individually and as part of a team.
Job Type: Fixed term contract
Contract length: 12 months
Schedule: Day shift, Monday to Friday
Work Location: In person
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