GMP OPERATOR (STERILE) - 12 MONTH CONTRACT

Dalton Pharma Services is looking for results-driven dedicated individuals, who are problem solvers and team players. This position requires working in the morning, afternoon or night shift and occasional weekend, or afternoon work required.

QUALIFICATIONS:

• High school diploma
• Basic Microbiology knowledge
• Knowledge of GMP regulations
• Working experience in a GMP manufacturing environment. Aseptic experience will be an asset.
  While we appreciate all applications received, only those selected for an interview will be contacted.
  We are committed to providing accommodations for applicants with disabilities. If you require accommodation during the recruitment process, please contact careers@dalton.com
  Job Types: Full-time, Fixed term contract
  Contract length: 12 months
  Pay: From $21.00 per hour

Benefits:

• Casual dress
• Company events
• Flexible schedule
• On-site parking

Application question(s):

• Are you comfortable working 100% on site?

Experience:

• Aseptic: 2 years (preferred)
• working in a GMP manufacturing environment: 2 years (required)

Work Location: In perso

• Participate in production processes (Formulation, Filtration, Filling, product Inspection and packaging), activities, as the project requires.
• Participate in visual Inspection, labelling, secondary packaging and final bulk packaging.
• Wash and autoclave equipment and glassware used in GMP production activities, including terminally sterilizing of filled products.
• Participate in general maintenance of the GMP environment.
• Clean/Sanitize and maintain production suites and support areas as required.
• Operate all machinery and related equipment involved in the GMP production activities.
• Complete GMP non-aseptic processes in accordance with current SOPs, worksheets, batch records and governing protocols.
• Complete documents in accordance with GMP regulations.
• Maintain logbooks documenting sanitization, equipment maintenance and calibration in accordance with GMP regulations.
• Reconcile and dispose of waste products in accordance with current SOPs and batch records.
• May participate in process development and other related studies.