Job opportunity
Supervisor, Sterile Dosage Production - Night
Norwell Inc.
Job Category
:
Manufacturing
Requisition Number
:
SUPER004083
Posted : October 26, 2026
Full-Time
On-site
Locations
Showing 1 location
Description
Material Resource Management:
Plan and organize the use of resources including equipment and labor to optimize the execution of daily operations and meet the delivery dates of external customers;
Respect the standards of efficiency, cleanliness during the cleaning of production areas and / or preparation of equipment;
Manage and resolve any emergency situation in order to respect the production plan
Quality and Compliance Management:
Ensure that the operations as a whole are performed as described in the procedures and that they comply with Good Manufacturing Practices, as well as Canadian, US and European standards;
Human Resource Management :
Manage, motivate and develop team members to achieve defined goals
Evaluate the performance of the employees under his responsibility according to the annual performance targets set.
Apply and ensure compliance with Health & Safety rules. Develop a health and safety culture at the plant level
Management of continuous improvement:
Define team-specific performance indicators such as production rejects, number of deviations, broken equipment, etc. ; see to their implementation and ensure their follow-up.
Inter-sector coordination:
Coordinate with the "Support" sectors when necessary, among other things, when implementing new products, equipment and / or problem solving.
Authority:
Has the authority to stop production activities according to emergencies
Escalade any issues specific to the production including the rejections of potential lots or any situation that may put at risk the health and safety of individuals, sterility or compliance activities.
Skills, knowledge and abilities:
High degree of motivation, initiative and creativity;
Excellent communication and interpersonal skills.
Patience, diplomacy and sensitivity to customer needs;
Ability to manage priorities and focus on results;
Autonomy, a great sense of organization, a great ability to manage and coordinate several projects and / or tasks simultaneously as well as a good resistance to stress;
Mastery of software on Windows environment; SAP, Trackwise
Excellent knowledge of French (oral and written) and good knowledge of English (especially oral).
Qualification in media fill (filling with culture environment)
Qualifications
Education
Required
Bachelor or better in Science or related field.
Experience
Required
5 years:
years of experience in the pharmaceutical industry
Experience in a sterile environment
Required experience in human resources management
Very good knowledge of Good Manufacturing Practices and Canadian Standards
Preferred
Knowledge of the standards of the F.D.A.
#J-18808-Ljbffr
Apply on source site :
Manufacturing
Requisition Number
:
SUPER004083
Posted : October 26, 2026
Full-Time
On-site
Locations
Showing 1 location
Description
Material Resource Management:
Plan and organize the use of resources including equipment and labor to optimize the execution of daily operations and meet the delivery dates of external customers;
Respect the standards of efficiency, cleanliness during the cleaning of production areas and / or preparation of equipment;
Manage and resolve any emergency situation in order to respect the production plan
Quality and Compliance Management:
Ensure that the operations as a whole are performed as described in the procedures and that they comply with Good Manufacturing Practices, as well as Canadian, US and European standards;
Human Resource Management :
Manage, motivate and develop team members to achieve defined goals
Evaluate the performance of the employees under his responsibility according to the annual performance targets set.
Apply and ensure compliance with Health & Safety rules. Develop a health and safety culture at the plant level
Management of continuous improvement:
Define team-specific performance indicators such as production rejects, number of deviations, broken equipment, etc. ; see to their implementation and ensure their follow-up.
Inter-sector coordination:
Coordinate with the "Support" sectors when necessary, among other things, when implementing new products, equipment and / or problem solving.
Authority:
Has the authority to stop production activities according to emergencies
Escalade any issues specific to the production including the rejections of potential lots or any situation that may put at risk the health and safety of individuals, sterility or compliance activities.
Skills, knowledge and abilities:
High degree of motivation, initiative and creativity;
Excellent communication and interpersonal skills.
Patience, diplomacy and sensitivity to customer needs;
Ability to manage priorities and focus on results;
Autonomy, a great sense of organization, a great ability to manage and coordinate several projects and / or tasks simultaneously as well as a good resistance to stress;
Mastery of software on Windows environment; SAP, Trackwise
Excellent knowledge of French (oral and written) and good knowledge of English (especially oral).
Qualification in media fill (filling with culture environment)
Qualifications
Education
Required
Bachelor or better in Science or related field.
Experience
Required
5 years:
years of experience in the pharmaceutical industry
Experience in a sterile environment
Required experience in human resources management
Very good knowledge of Good Manufacturing Practices and Canadian Standards
Preferred
Knowledge of the standards of the F.D.A.
#J-18808-Ljbffr