Sr. Associate, Quality Assurance

Found in: Jooble CA O C2 - 1 week ago

Brantford ON, Canada SC Johnson Professional™ Full time

Sr. Associate, Quality Assurance page is loaded Sr. Associate, Quality Assurance Apply locations CAN - Ontario - Brantford time type Full time posted on Posted 2 Days Ago job requisition id 25850

Joining the team at SC Johnson Professional makes you part of a family company with a deep history in the professional market as a leading manufacturer of skincare, cleaning and hygiene products, and smart technologies. We provide solutions to Healthcare, Clean Industrial, Industrial, Office & Institutional, Hospitality & Travel, and Retail & Entertainment markets.

SC Johnson Professional is a business unit within SC Johnson, a family-owned and led company and leading manufacturer of quality, trusted products since 1886.

ABOUT THE ROLE

The purpose of this position is to perform day-to-day quality assurance and compliance activities.

KEY RESPONSIBILITIES

  • Prepare paperwork for finished product release (C of A's, release paper).
  • Participate in regulatory audits (FDA, Health Canada)
  • Review technical documents including packaging orders, batch records, QC testing (bulk, finished product and raw materials), packaging components, stability and validation testing.
  • Co-ordinates change control and CAPA activities by assigning change control & CAPA numbers, distributing change controls for review and approval, and follow-up with the required activities for change control& CAPA closure.
  • Work with department managers to ensure the compliant execution of the training program.
  • Conduct internal audits and issue reports to management assuring compliance with company SOPs/policies and regulations.
  • Conduct deviation investigations, with the aid of involved department personnel, identify the root cause, required corrective action and/or preventative actions.
  • Assist in the generation and review of SOPs and associated controlled documents.
  • Develop and implement standard operating procedures.
  • Monthly documentation review for compliance to quality systems and predefined specifications.
  • Issue technical documents such as working batch records and packaging records to production.
  • Control and maintain current master indexes.
  • Perform inspections and line clearances according to approved manufacturing and packaging records.
  • Participates in investigation and follow-up for non-conformances (OOS and OOT).
  • Perform and assist in Customer Complaint investigations.
  • Initiates Vendor Complaints and follows up on vendor’s implementation of corrective actions
  • Co-ordinate and organize product launches, documentation related activities.
  • Write Annual Product Quality Reports (APQRs) for product consistency regarding their quality, including the deviations, change controls and customer complaints. APQRs are sent to related customers.
  • Review and/or approve technical documents (Certificates of Analysis, MWBR, MPO) in absence of Supervisor, QA
  • Other duties as assigned.

REQUIRED EXPERIENCE YOU’LL BRING

  • Minimum Bachelor of Science degree obtained through accredited university with minimum 3 – 5 years work experience.
  • Quality Assurance experience in a GMP environment

PREFERRED EXPERIENCES AND SKILLS

 

  • Thorough knowledge of applicable regulatory and industrial standards as it relates to cGMP and GLP.
  • Ability to organize and manage multiple priorities
  • Workplace Hazardous Materials Information Systems (WHMIS) training,
  • Organizational skills to handle multiple tasks.
  • Working knowledge of SC Johnson Professional product line.
  • Strong interpersonal skills required to effectively liaise with manufacturing staff, administration staff and external contacts.
  • Good Verbal and written communication skills in dealing/corresponding with outside contacts and internal staff.
  • Good judgement and problem solving skills necessary when dealing with results that require modifications/resolving.

JOB REQUIREMENTS

8 hours per day. Normal working hours are 8.5 hrs as assigned by the Associate Manager, Quality with a 30 minute lunch break, and two 15 minute breaks, Monday to Friday. 40 hours per week with overtime if and when required.

Inclusion & Diversity

We believe Inclusion and Diversity is more than a program. We embed inclusive practices in our day-to-day work, the way we relate to our colleagues, collaborate, and make decisions.

We value the collective richness of the differences people bring to the organization, including style, personality, thoughts, race, ethnicity, culture, religion, gender, gender identity, sexual orientation, age, and disability – that enables all to bring their full contributions to the organization.

SC Johnson & Son Inc., SC Johnson Professional, and SC Johnson Lifestyle Brands is committed to accessibility in its workplace and recruitment processes for persons with disabilities. If you require accommodation in order to participate in this recruitment process, please contact Human Resources.

About Us

Joining the team at SC Johnson Professional makes you part of a family company with a deep history in the professional market as a leading manufacturer of skincare, cleaning and hygiene products, and smart technologies. We provide solutions to Healthcare, Clean Industrial, Industrial, Office & Institutional, Hospitality & Travel, and Retail & Entertainment markets.

SC Johnson Professional is a business unit within SC Johnson, a family-owned and led company and leading manufacturer of quality, trusted products since 1886.

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