Canada

Animal Husbandry Technician (Ref#: C07-08)
Responsibilities:
General housing and husbandry;
Animal handling and restraint;
Cage changing and washing;
Autoclaving;
Glassware cleaning;
Sanitation of the animal facility;
Record keeping and inventory maintenance;
Equipment operation and maintenance.
The ideal candidate will possess the following:

Education/Experience

High school diploma and relevant experience;
Specific Skills

Good organizational and communication skills;
Ability to multi-task and work both individually and as team member;
Candidate must be able to lift up to 40 pounds and withstand repetitive bending and reaching up to 6 feet.

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Animal Care Technician (Ref#: C07-07)
Responsibilities:

General husbandry, housing and identification of experimental animals;
Animal health care, disease detection, treatment, and euthanasia;
Animal handling and restraint;
Surgery and post-operative care;
Assist the scientific staff in the conduct of scientific projects;
Equipment operation and maintenance;
Sanitation of the animal facility;
Laboratory procedures;
Record keeping and Quality Assurance;
Inventory maintenance

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CPL is a contract manufacturer and packager of prescription and over the counter pharmaceutical products. We are dedicated to providing comprehensive and innovative outsourcing services that exceed the uncompromising demands of the global pharmaceutical industry.

SENIOR BUYER
An exciting opportunity exists to support and collaborate with the Materials Management team in a dynamic and expanding contract pharmaceutical manufacturer. In this role you will source, purchase and expedite packaging materials in order to meet production requirements.

Key Responsibilities:
Evaluate material needs and purchase packaging components accordingly to satisfy production requirements while balancing cost and inventory considerations.
Negotiate favorable pricing and terms with approved suppliers.
Develop and maintain relationships with suppliers.

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CPL is a contract manufacturer and packager of prescription and over the counter pharmaceutical products. We are dedicated to providing comprehensive and innovative outsourcing services that exceed the uncompromising demands of the global pharmaceutical industry.

QA ASSOCIATE – SUPPLIER QUALIFICATION

An exciting opportunity exists to support and collaborate with the Quality team in a dynamic and expanding contract pharmaceutical manufacturer. In this role you will be instrumental in establishing and maintaining a raw material vendor certification program.

Key Responsibilities:
Develop, implement and maintain a vendor certification program in compliance with regulatory and cGMP requirements.
Prepare, revise and/or review SOP’s.
Identify, assess and determine existing or potential new material subject to inclusion in the certification program.

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:

Prepare and revise analytical forms for laboratory analyses based on approved test methods and monographs.
Maintain systems for control, issuance and reconciliation of analytical forms.
Coordinate the preparation and issuance of forms and worksheets with sample receipt to ensure documentation is available to the laboratory in a timely manner.
Maintain custody of original copies of approved test methods and monographs.

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This newly created position is a key member of the Engineering leadership team and will be responsible for:

· Planning & execution of engineering activities to meet divisional & corporate objectives.

· As a participative leader you will define a path to deliver World Class Manufacturing performance.

· Act as a liaison regarding technical and operational matters in conjunction with other divisional operations, technology partners, licensees and regulatory agencies to support the operation.

· Collaboratively develop solutions for facility issues.

· Produce innovative cost effective solutions to operational problems.

The successful candidate will have a Degree in Engineering coupled with over seven (7) years experience in an Engineering leadership capacity. Registration as a Professional Engineer or eligible for registration with APEGM is preferred.

Provide Mechanical Engineering Design and Project Management services for all additions and modifications to the physical plant, utilities, equipment installations and major repairs.
Technical input on design and specification stage up to and including qualifications.
Provide project management for physical plant, designing, specifying and overseeing the installation and start-up of all related equipment and systems.
Review, inspect and verify contractors/suppliers ensuring materials and resources are provided as required.
Prepare and oversee the completion of standardized documentation for installation and operation qualifications as required.

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Daily operation and maintenance of all building equipment and systems including but not restricted to steam boilers, hot water boilers, chillers, cooling towers, potable/purified water systems, compressed air, vacuum, dust collection and air handling systems.
Complete associated water testing and test procedures. Complete all required logs and other documentation accurately and on a timely basis.
Maintain building environmental conditions at required levels within designated production areas in accordance with department operational guidelines.
Maintain work areas, materials, tools and equipment to ensure serviceability, cleanliness and safety.
Maintain the fire protection/alarm system in proper working order.
Provide emergency response services to fire protection/alarm system and boiler operation.
Follow all department practices and procedures including the safe handling of reagents, solvents and equipment.

Assemble manufacturing equipment and complete installation utilizing layout plans.
Complete scheduled and unscheduled calibrations and maintenance and maintain records compliant with cGMP guidelines.
Follow up on irregularities or malfunctions of equipment operation.
Trouble shoot and repair mechanical, electrical, electronics, pneumatic and hydraulic problems.
Machine, weld and fabricate parts during set-up, maintenance or overhaul of manufacturing equipment or for building maintenance.
Ensure appropriate information concerning equipment operation and minor maintenance requirements is conveyed to manufacturing personnel on a timely basis.
Technical liaison sourcing and placing orders for parts and supplies and ensuring that manufacturing equipment is fully maintained.

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Review and approve facility protocols and reports associated with validation activities for cleaning, computer, methods and process validations including installation, operation and performance qualification for equipment, facilities and utilities.
Prepare, update and approve validation master plans (VMP), Site Reference Files, Quality Agreements, Annual Production Quality Reviews Summaries and Compliance Plans for the facility.
Participate in self-inspection and vendor audit programs to support validation review as scheduled.
Perform gap analysis of site procedures in relation to Global Policies and recommend required revisions.

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