As an Analytical Supervisor with a M.Sc. or Ph.D. in chemistry you have 5 - 10 yrs experience in either a quality control laboratory in a pharma company, Regulated Environment or Food GMP Industry, strong working knowledge of Canadian and U.S. GMPs, experience with quality control equipment and method development and validation, experience with HPLC, GC, ION exchange, raw materials, intermediates, finished product testing according to USP and other validated methods, strong oral and written English communication skills, working knowledge in TPP, ICH,USP and FDA method validation guidelines.
As an Analytical Chemist with a minimum of B.Sc. or M.Sc. in analytical chemistry or related principle and 5+ years analytical chemistry experience in the pharmaceutical industry, you are logical and have excellent oral and written communication skills. You have great accuracy and precision in all testing that you conduct and interpretation of analytical data and technical report writing are your forté.
You will be required to conduct method development, validation as well as routine testing using a wide variety of equipment including HPLC, GC (including capillary column and headspace), UV-vis, FTIR, as well as carry out wet chemistry analysis. Thorough understanding of GMP regulations, USP testing requirements and ICH guidelines is an asset.
Senior Analytical Chemist
As a Senior Analytical Chemist with a M.Sc. or Ph.D. in chemistry and 7+ years’ experience using HPLC and GC in the pharmaceutical industry, you are logical and have excellent oral and written communication skills. You have great accuracy and precision in all testing that you conduct and interpretation of analytical data and technical report writing are your forté.
You will be required to conduct the following:
Testing using a wide variety of equipment including HPLCs with UV, DAD, ELSD and electrochemical detectors, GCs (including capillary column and headspace) with FID and TCD detectors, Karl-Fischer, UV-vis, FTIR, oxygen headspace, Osmometer, automatic titrators, oxygen analyzers, pH meters
Carry out wet chemistry analysis
Participation in development and validation programs
Develop various methods for determination of different chemical entities and their properties, such as small molecules, peptides, proteins, DNAs and RNAs
You may have opportunity to participate in project coordination, helping supervisor to oversee Analytical progress
Production Manager - Sterile
We are currently looking for an experienced Product Manager for our growing sterile drug product manufacturing division.
The role requires extensive experiences in aseptic processing and manufacturing of sterile products, strong Project Management skills and the coordination of equipment, materials, manpower and documentation. It also requires strong management skills to lead a team of dedicated professionals.
You are focused, task driven, and committed on timely completion of client projects. You thrive on complexity and will be responsible for troubleshooting and optimizing batch production in a fast paced environment.
Thorough knowledge and understanding of cGMPs, and experienced with regulatory inspections, including Health Canada and FDA, are required.
The position requires a science degree, in chemistry or Microbiology, at least 10 years’ experience in pharmaceutical industry, including at least 4 years at a supervisory level.
Willingness to work under a 24/7 schedule, when required, is a must.
Business Development Representative
We are currently seeking an energetic Business Development Representative for our global sales team. The focus of the role is to identify and develop new contract development and manufacturing business that fits the technical expertise of the company. Scientific background and prior business development or sales experience preferred. The position will require some travel, including some international trips.
The successful candidate must have excellent communication and presentation skills and be extremely self-motivated.
Excellent English verbal and written skills.
Bilingual English and French verbal and written skills are preferred
Excellent presentation, interpersonal and communication skills
Previous pharmaceutical experience in a customer facing business role is strongly preferred. .
Extremely self-motivated, enthusiastic individual with strong initiative.
Strong time management and organizational skills.
Ability to multi-task.
Strong work ethic.
Ability to work independently and as part of a team.
Ability to network, develop new contacts, and manage relationships
Degree in Science (B.Sc. or M.Sc)
Experience in sales or business development role preferred.
Strong ability to positively influence others through establishing credibility and building strong business relationships.
Knowledge of contract manufacturing (CMO or CDMO) industry preferred
Ability to travel to international conference and industry meetings
Materials Department Associate
The Materials Department Associate facilitates the overall handling, movement and control of all materials, including hazardous materials, as per our SOP’s, within the facility executing all duties under the scope of Materials Management.
The Materials Department Associate performs the physical and/or administrative tasks involved in the purchasing, expediting, receipt and distribution of all inbound materials. This position receives all incoming goods, checks for accuracy against packing slips, prepares goods for shipment and enters all relevant information into electronic shipping/receiving system. The Materials Department Associate prepares packages and ships all finished goods, including hazardous materials and assists in the transportation function of the company. All above duties will be performed compliantly as per our internal SOP’s.
To qualify for this position, the candidate must have a High School Diploma (or equivalent degree) and 2 -5 years of relevant work experience with a focus on hazardous and regulated materials. Knowledge of international shipping/receiving regulations and requirements is an asset.Sound verbal and written communication skills are also required.
Qualifications & Experience
Relevant experience in a pharmaceutical environment an asset
Knowledge or experience working within GMP’s an asset
Knowledge or experience working with Dangerous Goods an asset
Knowledge of international shipping/receiving regulations is an asset
English spoken and written language skills essential
Must be able to deal with a high volume of requests