Job Description

About Us:

Northern RNA Inc. is a new Canadian CMO specializing in the production of nucleic acid products that support life-enabling work. Our goal is to collaborate with our customers to provide scalable manufacturing capacity and to help them accelerate innovation in bringing their products from benchtop to bedside or field.

About the Opportunity:

We are seeking a QC Associate to join our Quality Control team at Northern RNA. The Quality Control (QC) Associate plays a vital role in ensuring that all products and processes meet strict quality specifications and regulatory guidelines. This position involves performing a wide range of analytical and functional tests on raw materials, in-process samples, and finished goods. The ideal candidate will be a meticulous and highly organized individual with a strong foundation in molecular biology and a commitment to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP)

The candidate will work collaboratively with our multidisciplinary team of chemists, bioprocessing engineers, R&D scientists, and the manufacturing department during the analysis of samples related to the activities at Northern RNA.

Activities in this role:

Analytical Testing & Quality Control

Execute routine

in-process, release, and stability testing

on biological and chemical products. Perform various analytical techniques, including

High-Performance Liquid Chromatography (HPLC)

and

spectrophotometry

. Conduct

cleaning verification

and

environmental monitoring

tests. Assist with the

qualification and validation

of analytical methods (e.g., HPLC, Capillary Electrophoresis, ELISA, Bioassay, compendial methods) and prepare/review the associated documentation to ensure compliance.

Research new methodologies

and develop product-specific assays to support QC release testing and specifications.

Laboratory Operations

Prepare and document

reagents, media, buffers,

and laboratory stock solutions. Provide general laboratory support, including

organizing workstations, ordering supplies,

and performing

waste disposal

. Perform

equipment calibration, troubleshooting,

and

preventative maintenance

as required.

Documentation & Compliance

Participate in drafting documentation and reports in accordance with

Good Documentation Practices (GDP)

.

Education, Work Experience, Knowledge, and skills:

M.Sc. or PhD in the biological or chemical sciences (e.g. biochemical engineering, chemistry, molecular biology, biochemistry, or equivalent)
Work Experience:

At least 5 years of work experience in a controlled manufacturing or QC environment is required
Knowledge and Skills:

Demonstrated experience with development, validation, transfer and lifecycle of analytical methods used in biologics process development and/or manufacturing environment. Knowledge and experience working under GMP and regulatory standards is a plus Experience with routine analytical techniques is an asset (e.g. HPLC, UV spectrophotometry, pH, conductivity, plate assays) Knowledge and experience working under GMP and regulatory standards is a plus Meticulous at keeping records and highly organized Demonstrated ability to work independently, multi-tasking and meet assigned deadlines Strong sense of personal responsibility Excellent written and oral communication skills
Working conditions:

Ability to work in a manufacturing environment with hazardous materials and industrial equipment.
What do we offer?

We offer a highly competitive salary and company-paid benefits. Additionally, there are excellent opportunities for learning and growth while collaborating with our teams of experts who are bright, collegial, and highly motivated and who are on the cusp of the mRNA vaccine science and technology era.

Benefits:

Northern RNA Inc. offers its employees a wide range of benefits such as Health, Dental, Basic Life Insurance, General Illness (Long Term Disability), Vacation, Performance Bonus, on-site parking and Accidental Death and Dismemberment.

Additional Information:

Northern RNA Inc. requires all new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Northern RNA Inc. will consider requests for Reasonable Accommodations. Northern RNA Inc. requires all employees to wear a face covering (mask) in indoor public premises. Location for this position is in Calgary, Alberta. Candidates must be located within commuting distance or be willing to relocate to this area. Canadian citizens and those legally entitled to work in Canada are encouraged to apply. We are currently unable to sponsor.
Northern RNA Inc. is committed to a diverse and inclusive workplace. Northern RNA Inc. is an equal opportunity employer and does not discriminate based on race, religion, color, national origin, gender, gender identity, gender expression, sexual orientation, age, marital or veteran status, pregnancy or disability or other legally protected status. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs.

Offer of employment is conditional upon the completion of all applicable background checks and confirmation of credentials, the results of which must be satisfactory to the employer. We thank all applicants for the interest, however, only those selected for an interview will be contacted.

Job Types: Full-time, Permanent

Benefits:

Dental care Extended health care Life insurance On-site parking Paid time off Relocation assistance Vision care Wellness program Work from home
Ability to commute/relocate:

Calgary, AB: reliably commute or plan to relocate before starting work (required)
Education:

Master's Degree (required)
Experience:

Quality Control in cGMP/Pharma/Biotech: 5 years (required) Biopharmaceutical Manufacturing: 5 years (required) Quality Control: 5 years (required)
Work Location: In person