Quality Laboratory Supervisor (Second Shift), Johnson & Johnson Inc., Guelph, ON-4227140602
Description
Johnson & Johnson Inc. is a member of the Johnson & Johnson Family of Companies, the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. In Canada, Johnson & Johnson Inc. markets innovative consumer products focusing on skin and hair care, baby care, wound care, oral health and women's health as well as a broad range of well-known and trusted over-the-counter products through our McNeil Consumer Healthcare division.
At Johnson & Johnson Inc. our purpose is to "Bring Science to the Art of Healthy Living" by providing Canadians with some of the most world's most widely used and trusted brands including; JOHNSON'S ® Baby, NEUTROGENA®, AVEENO® LISTERINE®, BAND-AID® Brand Adhesive Bandages, TYLENOL®, REACTINE® , BENYLIN® , NICORETTE®, NICODERM® and many more. Based in Markham, Ontario, Johnson & Johnson Inc. employs approximately 400 people and is supported by a manufacturing and R&D facility located in Guelph, Ontario.
ROLE SUMMARY
We are currently recruiting for a Quality Laboratory Supervisor to join our team, for the Afternoon Shift working from 2:45pm to 11pm.
To support the McNeil Guelph site’s Reliability Manifesto and Unit Fill Rate (UFR), the Quality Sciences and Compliance Laboratory is recruiting for a Quality laboratory Supervisor. This individual will take a leadership role in the planning and coordination of team activities to ensure the timely analysis of raw materials, packaging components, bulk work in-process, and finished goods. The Supervisor will also be responsible for the analytical review, technical services and calibration functions of the Quality Sciences and Compliance Laboratory. Other key responsibilities of this position include, coaching, development and training of technical personnel in the department, assessment of specifications, department standard operating procedures and on-going evaluation and continuous improvement of Quality Sciences & Compliance activities.
MAJOR RESPONSIBILITIES
The responsibilities of this position include strong leadership, partnering, problem solving and communication skills.
Responsible for the scheduling of work to direct reports including the testing and review of active pharmaceutical ingredients (API’s), excipients, packaging components, semi-finished goods and finished product batches.
Performance management and development for team members (analysts, calibration services, technical services and reviewers).
Recommend and implement continuous improvement projects (CIPs) and Lean initatives related to product quality, methods and laboratory equipment.
Establish and modify department procedures (test methods, SOPs) that will satisfy company GMP, quality, environmental, safety and company standards.
Provide technical expertise in the team and to customers in R&D, Quality and Manufacturing, including review of cleaning validation, calibration procedures, preventative maintenance procedures, change controls, quality notifications, raw material method verifications, analytcial method transfers, equipment validation, and packaging changes.
Coordinate testing between day and second shifts.
Will assist management through change and transformation activities, and support strategic and tactical plans in alignment with site's goals.
Qualifications
EDUCATION AND EXPERIENCE
B. Sc. in Chemistry, Microbiology, Engineering or related Science
Qualified by training and experience as defined by the HPFBI
Minimum of 3 to 5 years relevant experience in a Quality, R&D or Production environment in the pharmaceutical, food or water industries. Previous supervisory experience is a definite asset.
COMPETENCIES
In-depth knowledge of Good Manufacturing Practices (GMPs)
Working knowledge of SAP and computer applications.
Knowledge of Process Excellence tools, thinks analytically and acts decisively.
Strong interpersonal skills and effective performance management skills
Ability to work on multiple projects simultaneously
Strong problem solving, partnering, communication and interpersonal skills.
BE VITAL in your career. Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
Diversity and inclusion are central elements of the shared culture across the Johnson & Johnson Family of Companies. Attracting, developing and retaining a workforce that reflects the diversity of our customers and communities is essential to our success. We are committed to providing a respectful, inclusive and accessible work environment where all employees have the opportunity to achieve their potential.
J2W:LI
Primary Location:North America-Canada-Ontario-Guelph
Organization: Johnson & Johnson Inc. (7695)
Job Function: Quality Control
Description
Johnson & Johnson Inc. is a member of the Johnson & Johnson Family of Companies, the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. In Canada, Johnson & Johnson Inc. markets innovative consumer products focusing on skin and hair care, baby care, wound care, oral health and women's health as well as a broad range of well-known and trusted over-the-counter products through our McNeil Consumer Healthcare division.
At Johnson & Johnson Inc. our purpose is to "Bring Science to the Art of Healthy Living" by providing Canadians with some of the most world's most widely used and trusted brands including; JOHNSON'S ® Baby, NEUTROGENA®, AVEENO® LISTERINE®, BAND-AID® Brand Adhesive Bandages, TYLENOL®, REACTINE® , BENYLIN® , NICORETTE®, NICODERM® and many more. Based in Markham, Ontario, Johnson & Johnson Inc. employs approximately 400 people and is supported by a manufacturing and R&D facility located in Guelph, Ontario.
ROLE SUMMARY
We are currently recruiting for a Quality Laboratory Supervisor to join our team, for the Afternoon Shift working from 2:45pm to 11pm.
To support the McNeil Guelph site’s Reliability Manifesto and Unit Fill Rate (UFR), the Quality Sciences and Compliance Laboratory is recruiting for a Quality laboratory Supervisor. This individual will take a leadership role in the planning and coordination of team activities to ensure the timely analysis of raw materials, packaging components, bulk work in-process, and finished goods. The Supervisor will also be responsible for the analytical review, technical services and calibration functions of the Quality Sciences and Compliance Laboratory. Other key responsibilities of this position include, coaching, development and training of technical personnel in the department, assessment of specifications, department standard operating procedures and on-going evaluation and continuous improvement of Quality Sciences & Compliance activities.
MAJOR RESPONSIBILITIES
The responsibilities of this position include strong leadership, partnering, problem solving and communication skills.
Responsible for the scheduling of work to direct reports including the testing and review of active pharmaceutical ingredients (API’s), excipients, packaging components, semi-finished goods and finished product batches.
Performance management and development for team members (analysts, calibration services, technical services and reviewers).
Recommend and implement continuous improvement projects (CIPs) and Lean initatives related to product quality, methods and laboratory equipment.
Establish and modify department procedures (test methods, SOPs) that will satisfy company GMP, quality, environmental, safety and company standards.
Provide technical expertise in the team and to customers in R&D, Quality and Manufacturing, including review of cleaning validation, calibration procedures, preventative maintenance procedures, change controls, quality notifications, raw material method verifications, analytcial method transfers, equipment validation, and packaging changes.
Coordinate testing between day and second shifts.
Will assist management through change and transformation activities, and support strategic and tactical plans in alignment with site's goals.
Qualifications
EDUCATION AND EXPERIENCE
B. Sc. in Chemistry, Microbiology, Engineering or related Science
Qualified by training and experience as defined by the HPFBI
Minimum of 3 to 5 years relevant experience in a Quality, R&D or Production environment in the pharmaceutical, food or water industries. Previous supervisory experience is a definite asset.
COMPETENCIES
In-depth knowledge of Good Manufacturing Practices (GMPs)
Working knowledge of SAP and computer applications.
Knowledge of Process Excellence tools, thinks analytically and acts decisively.
Strong interpersonal skills and effective performance management skills
Ability to work on multiple projects simultaneously
Strong problem solving, partnering, communication and interpersonal skills.
BE VITAL in your career. Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
Diversity and inclusion are central elements of the shared culture across the Johnson & Johnson Family of Companies. Attracting, developing and retaining a workforce that reflects the diversity of our customers and communities is essential to our success. We are committed to providing a respectful, inclusive and accessible work environment where all employees have the opportunity to achieve their potential.
J2W:LI
Primary Location:North America-Canada-Ontario-Guelph
Organization: Johnson & Johnson Inc. (7695)
Job Function: Quality Control