A career at Resilience is more than just a job – it’s an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit www.resilience.com

Position Summary

The incumbent will be responsible for testing in-process materials, validation, stability, and final products for bio-chemical and chemical assessment according to cGMP and company specifications. Responsibilities also include bio-analytical and analytical instrument qualification reviewing, training troubleshooting, instrument maintenance, high quality technical writing, leading and authoring Laboratory investigations, writing protocols / reports as well as cross-training of QC Technologists.

Position Responsibilities

• Perform sample analysis using bioanalytical test methods such as HPLC, UPLC, PCR, BCA, SDS-PAGE, ELISA, Western blot and UV-Vis, as per SOPs and / or protocols.
• SME for the assays performed, thorough theoretical understanding of the related concepts.
• Respond to internal and external auditors on questions on assays and instruments.
• Assist Lab management in internal, client and regulatory audits.
• Lead and Execute instrument qualification work as required.
• Develop and execute QC studies and write reports.
• Once qualified as a trainer, perform cross training of other personnel.
• Report to supervisor any deviations from company procedures, or other discrepancies that may affect product quality or cGMP status according to established procedures.
• Lead and author lab investigations and deviations by following sound scientific rationale.
• Perform routine maintenance on laboratory instruments.
• Follow established procedures for reference STDs receipt, inventory, use and discard.
• Troubleshoot methods and equipment as required.
• Author procedural changes using the change control program in Quality Management System.
• Review raw data and audit trails.
• Participate in scheduled cleaning and other laboratory housekeeping duties.
• Employ good documentation practices when generating raw data, reports, SOPs, and other documentation.
• Perform other routine testing after training to support analytical testing requirements in the lab.
• Ensure documentations and training are accurate and up to date.
• Assist in implementation of corrective action plans, participate in identifying root causes and communicate with other departments regarding pending issues.
• Able to apply understanding of regulatory guidelines and experience to documents and reports
• Performs all other related duties as assigned.
• Understanding of data integrity concepts and relevance to good documentation practices.
• Able to work flexible shifts and weekends as required.
• This role is a permanent afternoon shift

Minimum Qualifications

• Strong understanding of GMP, GLP, 21 CFR, ICH, Pharmacopeial and Regulatory guidelines.
• Advanced knowledge and practical experience in protein analysis HPLC/UPLC and PCR.
• Data analysis, statistics and report preparation with knowledge of MS Word, Excel and Outlook.
• Strong attention to detail, self-motivated, highly organized, and able to work in the fast-paced laboratory environment.
• Able to multi-task and very flexible based on the job priorities.
• Ability to learn new bioanalytical and analytical techniques quickly.
• Good verbal and written communication (technical writing/protocols/reports).
• Strong presentation skills.
• Strong instrument trouble shooting skills.
• High quality technical writing.

Preferred Qualifications

• Bachelor’s degree (Biochemistry/ Biotechnology/ Chemistry) with a minimum of 2 years related experience within a quality lab environment (biologics pharmaceutical preferred).
• Master’s degree (Biochemistry/ Biotechnology/ Chemistry) with 35 years related experience within a quality lab environment (biologics pharmaceutical preferred)
• Advanced knowledge and practical experience in protein analysis such as BCA, Western blot, SDS-PAGE, ELISA, concentration analysis using UV-Vis Spectrophotometer/Cell culture testing
• Very good knowledge in HPLC/UPLC/Plate readers/spectrophotometers
• Experience on advanced Bioanalytical instruments /HPLC/GC/Imager/IEF

Additional Requirements

• Pre-employment medical and medical re-examination; inclusive of eye examination and colour blindness test, performed every 2 years or as per Resilience’s SOPs
• This position requires vaccination for Hepatitis A and B
• Job requires shift work, weekends and occasional extended shifts and possible short notice schedule shift changes.

Resilience Biotechnologies Inc. (RESILIENCE), is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). Requests for accommodation can be made at any stage of the recruitment process. Applicants are asked to make their needs/requirements known to Human Resources.

Resilience offers employees a robust total rewards program including an annual cash bonus program, a RRSP/DPSP with a generous company match, a very competitive healthcare, dentalcare, vision care, life, LTD, and AD&D benefits package, fertility healthcare and family-forming benefits, paid vacation, paid holidays, pregnancy and parental leave top-up plan, tuition reimbursement, and employee referral program. Our target base pay hiring range for this position is $70,000.00 - $107,500.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.