Operational Quality Specialist

Bora Pharmaceuticals Services Inc

Mississauga

Hybrid

CAD 68,000 - 85,000

Full time

8 days ago

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Benefits offered by this job

Competitive salary
Health coverage
Retirement plans
Paid time off
Professional development
Wellness programs
Employee assistance

Job summary

Bora Bora Pharmaceuticals is seeking an Operational Quality Specialist to ensure products meet quality standards across QA processes, investigations, and batch release. You will support equipment qualification, deviations, change controls, and CAPA assignments, working in a hybrid setup with on-site presence.

Strong writing and regulatory knowledge are essential. The role offers a 37.5-hour week, competitive pay, and opportunities for professional development within a global CDMO environment.

Qualifications

  • Experience in Operational Quality Assurance or related role with similar responsibilities.
  • Minimum 2 years in Pharma industry.
  • Bachelor's degree in science / engineering / related field or equivalent on-the-job experience.
  • Preferred: College program completion for OQS role.
  • Adequate knowledge of regulatory framework and demonstrated ability to make informed decisions.
  • Ability to participate in projects or change initiatives with sound quality decisions.
  • Experience with SAP or similar systems and statistical software.
  • Strong communication and report-writing skills.
  • Able to work independently and in a team environment.

Responsibilities

  • Prepare and implement quality assurance procedures (SOPs) and review as required.
  • Investigate complaints, deviations, and product incidents; identify root causes and CAPAs.
  • Review IQ/OQ/PQ and process validation reports.
  • Review batch records and release or reject batches per procedures.
  • Participate in improvement projects for Quality systems and major changes.
  • Coordinate planned changes across units, suppliers, customers; ensure procedures followed.
  • Coordinate responses to audit observations and ensure recommendations are met.
  • Accountable for team and site metrics.
  • Participate in inspections as host, auditor, auditee, etc.

Skills

Interpersonal communication
Technical report writing
Team collaboration
Regulatory knowledge
Quality decision making
Independent work

Education

Bachelor's degree in science/engineering/related field
College program completion for OQS role

Tools

SAP

Job description

About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora's teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer's success more certain.

Position Status

This is a full‑time, permanent position that is currently vacant and approved to be filled as part of our ongoing staffing needs.

General Description

Operational Quality Specialists (OQS) ensure Bora's products and processes meet established quality standards. They provide quality support to a myriad of areas such as equipment qualification, validation, annual product reviews, deviations, change controls, complaints, Gembas, and batch record review and release. Their key responsibilities are listed but not limited to the following.

  • Prepare and implement quality assurance procedures (such as SOPs) and be responsible for reviewing as required.
  • Participate in investigation of complaints, deviations, and product incidents ensuring that all investigations are thorough, complete, identify root cause, and assign appropriate CAPAs.
  • Review documentation related to equipment qualification (IQ/OQ/PQ) and process validation, and preparation/review of reports.
  • Review batch records and associated documentation, releasing or rejecting batches as per quality procedure.
  • Participate in improvement projects for Quality systems and other special projects and initiatives, including new product introductions, significant changes to equipment/systems, etc.
  • Coordinate planned changes initiated by various business units, suppliers, as well as customers and ensure relevant quality procedures are followed.
  • Coordinate responses to internal improvement documents as required, such as audit observations, ensuring compliance to recommendations.
  • Accountable for team and site metrics.
  • Participate in inspections including roles such as hosting, mission control, auditor, auditee, etc.
Experience and Skills
  • Experience in Operational Quality Assurance or related role with similar responsibilities.
  • Minimum 2 years in Pharma industry.
  • Bachelor's degree in science / engineering / related field or equivalent on-the-job experience through years of service.
  • Preferred: College program completion for OQS role.
  • Adequate knowledge of regulatory framework and demonstrated ability to make informed decisions.
  • Demonstrated ability to participate in projects or change initiatives with the ability to make sound quality decisions.
  • Experience with statistical software, SAP.
  • Strong interpersonal and communication skills.
  • Excellent technical report writing and reviewing skills.
  • Able to work independently and in a team environment.
Working Conditions

37.5-hour work week in a hybrid work environment, with a minimum of three days onsite per week. Rotating afternoon shifts approximately every three months. Work will be performed in both production and office environments.

Additional Information

In accordance with Ontario's pay transparency requirements, candidates will be notified when they are no longer under consideration or once the vacancy is closed. Updates regarding application status may be communicated via email or through the online applicant profile, where applicable. As part of our recruitment process, we may use technology-assisted tools, including automated systems, to support the review and assessment of applications. These tools do not make final hiring decisions. All decisions related to screening, interviewing, and selection are made by our Talent Acquisition and hiring teams.

Compensation Range

$68,000-85,000

Benefits Include
  • Competitive salary and performance-based incentives
  • Comprehensive health coverage including medical, dental, and vision insurance
  • Retirement savings plans with employer contributions
  • Paid time off and flexible work arrangements
  • Professional development opportunities
  • Employee wellness programs and resources
  • Employee Assistance Program and Mental Health Resources
Our Values

At Bora, our values guide everything we do - from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.

We're proud to be an equal opportunity employer, committed to building a diverse and inclusive workplace where everyone feels empowered to contribute and grow. We welcome applications from qualified individuals of all backgrounds, experiences, and perspectives.

If you require accommodation during any stage of the application or interview process, or if you'd like to learn more about our accessibility policies, please contact us at accessibility@bora-corp.com.

Bora Pharmaceuticals is focused on developing and manufacturing branded, generic and over the counter (OTC) healthcare and pharmaceutical products for patients around the globe. At Bora Pharmaceuticals, we see it as our mission and our duty to make our mutual success more certain. As an ambitious, future-focused company, we know better than most that our own success is shaped by our partners victories.

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