About this role
Job#: 3057213
Job Description
Senior Chemist (QC)
Client: medical technology and medical device company
Contract duration: 14-month contract (potential to extend)
Location: Mississauga, Ontario
Pay Rate: $40-45/hr
Description of Position
Responsible for performing raw materials, finished product and stability testing and ensuring records associated with Quality Control are complete. Responsible for QC method validation (in conjunction with R&D), equipment calibration/qualification and troubleshooting. Will be asked to participate in out of specification, non-conforming material and deviation investigations. Will be required to provide training and guidance to the QC team and to perform some scheduling of tasks and follow-up on completion of work.
Key Accountabilities and Responsibilities
- Perform Routine, In-Process, release and stability testing, focused on simple bench tests. May be asked to perform more complex testing (, using more sophisticated equipment).
- May perform water bioburden testing and air sampling.
- Write, update and review QC SOPs and test methods as needed.
- Perform method validation/transfer sample testing when required.
- Work with R&D to ensure new validated methods are converted for GMP purposes.
- Develop stability schedule and monitor stability program. Review stability reports.
- Schedule QC testing to ensure timelines are met.
- May be asked to support equipment qualification, maintenance and the instrument calibration program.
- Responsible for maintaining accurate equipment records.
- Conduct out of specification investigations. Support or perform non-conformance and deviation investigations as needed.
- Mentor and support junior chemists, acting as a trainer and resource as they learn.
- Identify and implement improvements within the lab.
- Ensure safety procedures are being followed and dispose of lab waste appropriately.
- Aid in solving technical problems.
- Ensure work is in compliance with GMP and established SOPs.
- Store and keep track of finished product retention samples.
- Monitor and order required lab solutions and equipment needed for testing.
- Review test reports for QC testing.
Participate effectively as an employee of the company
- Immediately report to manager any delays in testing or if tasks cannot be completed.
- Work effectively in collaboration with other members of the department, or with managers and staff across the organization with whom tasks must be completed.
- Work in a safe manner so as not to endanger individual health and safety, or the health and safety of others.
- Work to achieve assigned tasks within the standards required (quality, quantity, time and resources).
- Comply with all legal requirements, all corporate policies and procedures, and with generally accepted business and ethical practices.
- Perform other duties as assigned by immediate manager.
Qualifications
Education
- Minimum a or equivalent undergraduate degree in chemistry/chemical or related engineering area or microbiology.
Knowledge/Experience
- Understand basic QC lab practice and GMP requirements.
- Minimum 4 year working experience in the chemistry or chemical engineering field.
Skills
- Proven good oral and written communication skills.
- Advanced computer skills, proficient in the Microsoft suite (WORD [create and use templates], EXCEL, and PowerPoint), Adobe Acrobat.
- Experienced in advanced analytical techniques such as HPLC, GC, ICP, etc.
- Detail oriented and excellent organizational skills.
- Analytical mindset and problem-solving skills.
- Ability to prioritize multiple tasks.
- Excellent written/oral communication and organiza