Septa Pharmaceuticals Inc.
7490 Pacific Circle, #1 L5T 2A3 Mississauga, ON, Canada
Category
General Information
Locality: Mississauga, Ontario
Phone: +1 905-564-5665
Address: 7490 Pacific Circle, #1 L5T 2A3 Mississauga, ON, Canada
Website: www.septapharmaceuticals.com
Likes: 80
Reviews
Facebook Blog
http://www.cmaj.ca//23oct13_Health-Canada-to-improve-drug-
WE ARE HIRING! International/National Sales Manager (Business Development) Visit link below to apply:... http://www.septapharmaceuticals.com/job.php?ID=4
http://chealth.canoe.ca/channel_health_news_details.asp
http://medicinehatnews.com//less-than-a-month-in-pharmaci/
http://globalnews.ca//province-gives-pharmacists-30-day-r/
http://www.therecord.com//880394--health-canada-announces-
WE ARE HIRING!!! We are excited to announce the opening for the position of Manager - Quality Control & Quality Assurance. Working to support operations and to ensure compliance as related to pharmaceutical products and regulations, the incumbent will principally be responsible for managing all QC/QA responsibilities as well as oversee the drafting and implementation of Standard Operating Procedures (SOPs) related to Operations. Essential Duties/Responsibilities:... - Abide by the laws and by-laws of the company and the country of operations acting as a role model setting corporate standards and expectations both, internally and externally. - Engage in the process of drafting, reviewing, and implementing SOPs for the Company’s Operations department. - Develop and conduct internal audits pertaining to company operations, presenting findings to the senior management. - Participate in any HPFBI inspections/audits, serving as a subject matter expert for any inquiries that arise during the inspection/audit, including the drafting of action plans (if required). - Monitor and perform GMP inspections to assess compliance with Division 2 of HPFBI with Operations. - Handle all product lot release activities, including the review of manufacturing and other documentation to support batch releases. - Work with Operations team to create necessary operational documents and transition daily support activities with team. - Proactively research, analyse and recommend updates and improvements to existing systems and/or SOPs. - Other duties, as assigned. Qualifications : - 6-7 years of experience in a related quality position with experience in Canadian Drug GMP. - Minimum B.Sc. from an accredited Canadian University (preference will be given to majors in Chemistry and/or Microbiology). - Solid knowledge base in GMP, Establishment Licensing, NHM GMP requirements and other activities related to Canadian Drug products. - Experience in reviewing master product documents and auditor training, including conducting third party audits. - Strong follow-through, strong attention to details, resourceful in resolving issues and troubleshooting questions and issues as they arise. - Excellent written and oral communication skills. - Proficient in Microsoft Word, Outlook, and Excel. - An aptitude for advancing community, social, and environmental interests through volunteering and mentoring initiatives. http://septapharmaceuticals.com/job.php?ID=13
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