Research Scientist - Microbiology

Apotex Fermentation Inc. (AFI), part of the Apotex group of companies, is Canada’s largest manufacturer of Active Pharmaceutical Ingredients by fermentation. AFI is looking for a Research Scientist to work in our Microbiology R&D laboratories to assist in developing fermentation processes for producing prescription drugs.

The successful candidate, having acquired an in-depth knowledge of assigned projects from Company sources, available patent and scientific literature, will plan, execute and report on laboratory trials (in cooperation with technical staff and management). Based on research data recommendations to management will be made on future trials and scale-up to lab-scale fermenters trials.

This is a permanent position and requires a minimum of a post-graduate degree (M.Sc. or higher in Microbiology or a relevant field of study) from a recognized university. In addition, written, spoken and computer-based communication skills are required as is the ability to communicate advanced scientific information. Related experience preferably in the pharmaceutical industry and a proven record of success in process development are an asset.

Salary will commensurate with qualifications and experience. An excellent benefits package is provided.

Apply before Friday, May 16, 2008.

Quality Control Chemist

As a member of the Quality Control & Methods Development Department, the Quality Control Chemist is responsible for the testing and analysis of raw materials, intermediates, finished products and stability samples using physical, chemical and instrumental techniques. The primary responsibility of this position is to perform sampling, testing and releasing raw materials. The successful candidate will operate analytical equipment such as FTIR/IR, HPLC, GC, IC and Karl Fischer. Other duties include writing; editing and reviewing SOPs, Protocols, Reports and other QC related documentation.

Qualifications:

• Qualified candidates will have a B.Sc. or College Diploma in Chemistry, Analytical Chemistry, or equivalent, with working experience in performing wet chemistry tests and operating analytical instruments.

• A familiarity with cGMP guidelines and experience in a regulated pharmaceutical environment is desired.

• The preferred candidate will be a team player with excellent organizational skills and the ability to work in a fast paced environment.

• A limited shift work (one in four weeks, evening shift) is required for this position.

This position reports to the QC Raw Materials Supervisor in the QC & Methods Development Department.

Apply before Friday, May 9, 2008.

3^rd Class Power Engineer

We require this individual to possess a sense of duty and responsibility with excellent problem solving abilities and the ability to be flexible and adaptable in a fast paced environment. We are looking for a team player that is detail oriented and thorough in their work and who possesses good verbal and written skills as well as basic computer skills.

Qualifications:

The successful candidate will have a 3^rd Class Power Engineering Certificate.

Responsibilities include but are not limited to:

• Understand and follow cGMP requirements as relates to equipment, processes, material and validation.

• Operation and performance of all pressure systems, including refrigeration systems, according to the Power Engineers Act.

• Ensure the preventative maintenance program is followed and kept current.

• Operate and repair the mechanical systems, compressors, HVAC, pneumatic controls, waters systems and plumbing systems.

• Assist Plant & Facilities Manager to carry out his duties and to communicate frequently the current status of area of control.

• Assist in overseeing work performed by outside contractors.

This position reports to the Power Engineer 3^rd Class/Supervisor in the Plant Engineering Department.

Apply before Friday, May 9, 2008.

Production Operators

You will be required to learn the operation of process equipment and general procedures in accordance with Good Manufacturing Practices (GMP) and Health & Safety requirements. Duties include process operations and process monitoring, troubleshooting, cleaning of equipment and work areas, and documentation. The ability to lift 50 lbs is a requirement. Shift work with 12 hours shifts and 24/7 coverage is mandatory.

Production Operators must have:

• Industrial / production experience

• a grade 12 diploma

• mechanical aptitude

• the ability to strictly follow written English instructions

• an excellent work ethic and common sense

• work well in a team environment

• basic computer skills

• GMP or ISO experience would be an asset.

Production Operators have an excellent starting salary above 30K. In addition, there is a shift premium for all hours worked, an increase at approximately six months and a benefits program.