Experience our tradition of excellence
CONSULTPHARM has been providing expert advice in regulatory affairs and quality assurance (GMP) to the pharmaceutical, natural health products and cosmetics industries since 1985. Consultpharm enjoys a reputation for quality, both within the industry and with Health Canada.
We are looking for a passionate person who strives for excellence and wants to join our dynamic team. This person will demonstrate professionalism and enjoy challenges.
Summary of tasks
Under the supervision of the QA Director, the ideal person:
Perform visual inspections of finished products and packaging components;
Perform preliminary verification of batch records;
Participate in the management of finished product stability programs;
Contribute to the verification and maintenance of finished product master records;
Maintain the quality assurance records archiving system;
Support the regulatory affairs department and the administrative team.
You are an autonomous, organized, rigorous and ambitious person. You want to work in an industry where standards are very demanding. You have:
A college diploma in science or a related field;
1 to 3 years experience in quality assurance of pharmaceutical, natural health and cosmetic products;
Fluency in both English and French, both written and spoken;
Very good knowledge and skills in computer science;
Ability to work independently from home (minimum supervision required);
Flexibility and adaptability;
Ability to meet deadlines;
A car and a valid driver's license;
A sense of organization and discipline;
Make a career at Consultpharm
We offer you a stimulating work environment as well as career development opportunities. What's more, you will benefit;
A permanent full-time job;
A group insurance plan;
A better work-life balance.
We thank all applicants, but only those selected for an interview will be contacted.