Search:
Pharmaceutical Contract Manufacturing Company
 

 
 
 

Careers

Dalton is always looking for new people to contribute to the company's growth. We offer a competitive salary and benefits and an excellent opportunity to build your career with a growing company.

Please forward your resume to:
 

Human Resources Department
Dalton Pharma Services Inc.
Fax: 416-661-2108


While we appreciate all applications received, only those selected for an interview will be contacted.
 

Learn more about our benefits.

 
POSITIONS CURRENTLY AVAILABLE:
 
Aseptic /Sterile GMP Operator

Qualified candidates will have a B.Sc. or College technical diploma in Microbiology or Related Science using Sterile techniques, preferably with over 3 years of related work experience.  Alternatively, a High School Diploma with over 5 years relevant sterile/aseptic manufacturing experience. The successful candidate will have excellent verbal and written communication skills with the ability to work in a team environment. Must be able to follow verbal and written instructions. This position may require shift work.
 

You must possess the following qualifications:

  • Previous experience Aseptic/Sterile Fill or Microbiology/Sterile techniques
  • Previous experience with sterile drug product formulation and filling
  • Good knowledge of microbiology is a plus
  • Control and maintain inventory of sterile material and equipment
  • Participate in sterile process operations (filtrations/formulations/crystallizations/fills)
  • Document work according to batch records and GMP requirements
  • Troubleshooting and problem solving capabilities
  • Work closely with a team of sterile operators
  • Perform all GMP activities in compliance with GMP guidelines & Dalton SOP’s

 
Quality Control Manager

We are seeking an experienced QC Manager to join our team. As a QC Manager you hold a PhD or MSc in Chemistry with 5-10 yrs supervisory or management experience in a GMP quality control environment.  You have had involvement directly leading FDA inspections with successful outcomes within in the past 3-5 years. Experience in OpenLab software and instrumentation validation is a requirement.  Able to develop, administer and coordinate the schedules and technical activities of the QC team.   Act as an advisor to help subordinates meet timelines and resolve technical problems.  Coordinate lab activities with other departments / supervisors to best serve both production and research needs. Strong working knowledge of GMPs, experience with quality control equipment and method development and validation.  You must possess strong oral and written English communication skills.
 

 

 

Customer Service Coordinator

A self-starter with high energy and initiative, you must have a Science degree with 3+ yrs office experience, superior organizational and interpersonal skills.
 

In this position will be responsible to provide Customer Service in support of Business Development and Sales functions. Experience with MS Dynamics and Salesforce.com (CRM) is an asset.

 

 
 

Home | Company | Services | Products | Resources | News | Careers | Accessibility | Contact