Quality Assurance Associate

Catalent Pharma Solutions; Strathroy; On-site; CAD 60,000 - 80,000; Full time

Job summary

Catalent Pharma Solutions is seeking a Quality Assurance Associate in Strathroy, Ontario. This role focuses on maintaining quality compliance within manufacturing operations by performing audits and training staff on quality practices. Join a leading organization dedicated to improving patient health through innovative pharmaceutical solutions.

Benefits

Comprehensive Benefit Package

Group Retirement Savings Plan

Employee Reward & Recognition programs

Opportunities for professional development

Qualifications

• Prior experience in manufacturing or GMP facility.
• Able to work independently with minimal supervision.
• Candidates with non-Canadian credentials must provide evaluation.

Responsibilities

• Perform in-process document auditing and product quality checks.
• Assist in investigation of manufacturing issues and deviations.
• Perform weekly compliance audits in production and packaging.

Skills

Analytical skills

Problem-solving skills

Detail-oriented

Interpersonal skills

Communication skills

Time management

Education

Bachelor’s degree in science or Engineering

Tools

MS Excel

MS Word

Job description

Quality Assurance Associate

Position Summary

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

This position is located in Strathroy, Ontario, one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.

Reporting to the Quality Assurance Supervisor, the Quality Assurance Associate creates a culture of quality compliance and continuous improvement, which meets the government, customer and business requirements. the focus is on prevention rather than detection of quality issues. In addition, the Quality Assurance Associate will perform final product audit for product release and coaching and training operators and supervisors on proper documentation practices and cGMP requirements.

12-hour Continental Shifts (Days and Nights)

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

The Role:

• Performs in-process document auditing and product quality checks in production and ensures all issues are communicated to production employees, production management and QA management.

• Performs Final Release auditing of batch documentation ensures all product has been manufactured in compliance with cGMP’s and SOP’s. This includes performing all duties required to release the final product.

• Assists in the investigation of manufacturing issues and manufacturing deviations as reported by the production departments.

• Performs in-process product quality checks and documentation review.

• Performs weekly compliance audits/monitoring in all production and packaging departments and prepares result reports for QA management.

• Acts as QA representative on shift in decision-making and issue resolution, escalating serious issues to production management and QA management as required.

• Performs line clearance verifications of equipment and processing areas during changeovers from one type of product to another type of product – may include testing/verification of vision equipment.

• Perform other duties as assigned.

The Candidate:

• Bachelor’s degree in science, Engineering (Chem., BioChem.) or related field is required.

• Prior experience in a manufacturing, pharmaceutical and/or GMP facility would be an asset.

• Strong analytical and problem-solving skills.

• Extremely detailed oriented.

• Excellent prioritization and time management skills.

• Strong interpersonal skills.

• Excellent communication skills – verbal and written.

• Able to work independently with minimal supervision.

• Advanced computer skills in MS Excel and Word.

• Currently Catalent does not participate in the Ontario Immigrant Nominee Program (OINP).

• Candidates with non-Canadian credentials must provide an evaluation confirming the Canadian equivalency of the credentials as determined by the Alliance of Credential Evaluation Services of Canada (ACESC) such as WES.

• The employee's role frequently involves sitting and utilizing hands and fingers for tasks such as handling, feeling, and keyboard manipulation, necessitating manual dexterity.

• Occasionally, the position requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, alongside close vision capabilities and potential exposure to chemicals.

Why You Should Join Catalent:

• Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)

• Group Retirement Savings –Registered Pension Plan (RPP) with employer contributions.

• Employee Reward & Recognition programs.

• Opportunities for professional and personal development & growth including tuition reimbursement.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.