Careers

Quality Assurance Administrator

Innopharm, a division of CPL, is a contract analytical testing laboratory that provides a wide range of services to the pharmaceutical industry. We are dedicated to providing comprehensive and innovative outsourcing services that exceed the uncompromising demands of the global pharmaceutical industry.
           
SPECIFIC RESPONSIBILITIES:

1. Prepare and revise analytical forms for laboratory analyses based on approved test methods and monographs.
2. Maintain systems for control, issuance and reconciliation of analytical forms.
3. Coordinate the preparation and issuance of forms and worksheets with sample receipt to ensure documentation is available to the laboratory in a timely manner.
4. Maintain custody of original copies of approved test methods and monographs.
5. Develop and maintain systems for indexing and archival of GMP documents and records.
6. Establish and maintain a control system for filing and retrieval of archived documents and records.
7. Responsible for promoting and maintaining safe and healthy working conditions in his / her assigned work area; instructs, enforces and evaluates employees under their supervision to work in compliance with established safe work practices and procedures; ensures workers receive appropriate training and information necessary to conduct their activities in a safe and healthy manner.
8. Other duties as assigned.

QUALIFICATIONS:

1. A College Diploma and a minimum of 1-2 years of experience in Pharmaceutical industry as document coordinator or equivalent experience is required.
2. Strong knowledge of cGMP, FDA and HPFBI.
3. Strong oral and written communication skills.

Interested applicants should submit a resume in confidence to:

Innopharm Inc.
1 Valleywood  Drive
Unit 100
Markham, Ontario
L3R 5L9
Attention:  Human Resources
Fax: 905-470-9241
E-mail: sschafron@cplltd.com

We thank all applicants in advance, however only candidates of interest will be contacted.  No telephone or agency inquires please.