QA Associate

Introduction

The QA Associate

will be responsible for

managing

documentation

, coordinating activities of staff,

and

monitoring the production of regulatory compliant product. The QA Associate

will provide assistance

to

the functions within the

Quality

Management

System

, and will be dedicated to

ensuring compliance

across

all departments. Reporting to the QA Supervisor

, the QA Associate

will be responsible for

ensuring that Good Production Practices

(GPP)

and

all

applicable regulations

laid out by the Cannabis

Act

are

adhered to

at all times
- The

extraction facility is located in Aylmer, Ontario.

Company

Motif Labs is a licensed cannabis extraction facility located in SW Ontario.

Motif operates as a businessto-business enterprise, offering toll processing and contract manufacturing services to Licensed

Producers (LP's) and 3rd Par

ty Brands.

Motif is experiencing significant growth and we are seeking

dynamic and professional individuals to join our team.

Motif prides itself on Integrity, Collaboration and

Quality, and these core values are at the center of everything we do.

Positi

on Overview:

- Ensure completeness and accuracy of

QA

documentation

, ensuring

Good Documentation

Practices on all applicable documents related to GPP
- Assist

with

managing the Quality Management System
- Draft

SOPs to ensure continuous compliance
- Ensure that cannabis, raw materials, and packaging materials are received and tested in

accordance with established procedures
- Investigate and complete deviation reports

, complaints, and CAPAs
- Review batch records

and Certificate

s of

Analysis

, ensuring

that product meets quality and

regulatory requirements
- Ensur

e that

all

staff are adhering to facility SOPs

and GPP

at all times
- Work with QA Supervisor

to develo

p, implement and conduc

t internal

facility audits as

scheduled
- Other job duties as assigned

Qualifications:

- Bachelor’s Degree

or College Diploma

in science or

a related discipline
- Minimum

1 year of experience working in Quality Assurance in a

GMP

/GPP

environment

,

pharmaceutical

and/or

food

and beverage

industry
- Experience

with

Quality Systems: Change Control, Deviation, CAPA, Document Control
- Ability to work in a dynamic environment and collaborate with a cross
- functional project team
- Highly organized with attention to detail for successfully satisfying diverse responsibilities
- Ability to read and correctly interpret documents such as safety rules, regulations, and

specifications
- Strong attention to detail, ensuring documentation is complete and accurate
- Strong written and verbal communication skills
- Flexibility to work varying

shift

schedules