SPONTANEOUS APPLICATION
Vous cherchez à poursuivre une carrière chez Macco Organiques, mais vous ne trouvez pas le poste que vous recherchez ? Envoyez-nous quand même votre curriculum vitae ! Nous le conserverons dans notre base de données pour les futures offres d’emploi qui pourraient vous convenir.
Shift premium
Pension plan
Telemedicine
Group insurance plan
Annual salary increase
Employee and family assistance program
WHY MACCO ORGANIQUES?
MISSION
Notre objectif est de nous entourer d’une équipe minutieuse et innovante afin d’offrir à nos clients des produits de qualité supérieure.
VISION
Macco Organiques met à profit sa solide expérience dans l’industrie alimentaire pour assurer la pérennité de ses opérations en augmentant sa présence sur le marché pharmaceutique.
VALEURS
- Qualité
- Rigueur
- Intégrité
- Passion
- Agilité
- Flexibilité
Available positions
Role and responsibilities:
- Product bagging in 20-25 kg bags (or balloons) according to approved work instructions and records;
- Complete the necessary documentation as required;
- Clean and/or maintain premises and equipment;
- Apply good manufacturing practices (GMP) and comply with health and safety, hygiene and environmental regulations.
- Be prepared to perform other related tasks on an individual basis and collaborate as a team.
Profile searched:
- High school diploma 5 (SDA) or equivalent (required);
- Must be at least 18 years of age when taking up your duties (required);
- Able to perform manual and repetitive tasks
- Ability to communicate effectively in French;
Role and responsibilities:
- Record and prepare samples
- Evaluate the physico-chemical characteristics of finished products;
- Inspect raw materials and finished products according to specifications;
- Record results and process computer data;
- Use, calibrate and maintain equipment (HPLC, ICP, IR, UV, AA
Profile searched:
- DEC in Analytical Chemistry;
- Has a minimum of one year’s experience in a similar industrial position;
- Knowledge of ISO and HACCP (an asset)
- Fluent in French and English, both spoken and written.
- Skilled with technological tools (computer, internet, various software).
Role and responsibilities:
- Schedule production based on order;
- Forecast demand and production constraints;
- Determine the order of production;
- Create and update production vouchers according to specific customer needs;
- Receive purchase orders and give confirmation to customers
- Establish and update the raw material and packaging requirements plan;
- Any other related tasks.
Profile searched:
- Diploma deemed relevant;
- Relevant experience in the area of planning;
- Ability to react quickly to unforeseen events;
- Ability to work with computer software
- Resourceful and open-minded
- Adept at applied problem solving and continuous improvement;
- Excellent analytical and synthesis skills;
- Develop organizational skills;
- Great availability to deal with various unforeseen events.
Role and responsability:
As a Quality Assurance and Training Specialist reporting to the Scientific Director in close collaboration with the various departments of the company, in an environment operating according to the common GMP Pharmaceuticals and FSSC 22000, the main functions will be:
• Plan and coordinate the training program in place.
• Review current training programs.
• Conduct training needs analysis ensuring that they are in line with regulatory requirements.
• Follow up on training documentation.
• Evaluate the effectiveness of the training program in place and propose improvements, when necessary during its life cycle.
• Participates in routine quality assurance tasks such as:
– Investigation
– Corrective actions
– Annual reports
– Trend Tracking
– Non-conformances, complaints and deviations
Desired profil:
• Minimum BA in chemistry, biochemistry, engineering or equivalent.
• Minimum of 2 years experience in a similar position.
• Good knowledge of training requirements in the pharmaceutical industry.
• Good knowledge of investigation processes in the pharmaceutical industry.
• Knowledge of current GMP regulations, FDA, Health Canada, European and ICH.
• Bilingual spoken and written (English/French) is required.
• Knowledge of FSSC 22000 would be an asset.