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Posted 19 days ago

Specialist, Quality Assurance (Investigations)

@ Sun Pharmaceutical Industries Ltd

Brampton, Ontario

1+ years experience
Apply now
SIGNALS

Overview

Sun Pharmaceutical Industries Ltd is hiring a Quality Assurance Specialist to lead deviation investigations, root cause analysis, risk assessments and CAPA effectiveness under GMP and regulatory requirements. The role is office based, with regular hours of 8:00am to 4:30pm plus extended hours for urgent issues. Base pay is $63,500 to $79,500 plus an annual performance bonus.

Responsibilities:

  • Prepare deviation investigation reports and identify root causes
  • Execute risk assessments based on investigation findings
  • Manage CAPA effectiveness and timely execution of actions
  • Coordinate subject matter experts and investigation boards
  • Support internal, customer and regulatory audits

Requirements summary:

  • Bachelor's degree in science or related discipline
  • Minimum 1 year in pharmaceutical QA, QC or manufacturing
  • Working knowledge of pharmaceutical quality systems
  • Experience with Health Canada and FDA officials
  • Experience in TrackWise is an asset

Tools & skills

Benefits mentioned

DentalVisionLife insuranceRetirement planEmployee assistance
Source and dates

Employer career site / ATS feed · successfactors

Employer posting date
2026-10-18
First seen by our source
2026-10-19
Source record updated
2026-10-19

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityEntry level
DepartmentQuality assurance
Experience1+ years
Hours per week40
Scheduleday, evening
Travelair: none · ground: none
Work settingOffice
PositionMostly sitting
Physical demandsphysical low · computer high
LanguagesEnglish
EducationBachelor’s degree (required)
Fields of studyScience
Perks mentionedGenerous paid time off, Retirement plan, Performance bonus, Wellness

Summary and details written by AI from the posting; the employer’s posting is the authority.

Sun Pharmaceutical Industries Ltd

Saved company profile

Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.

Reaching People. Touching Lives.

Full company description

Sun Pharma is the world's fourth-largest speciality generic pharmaceutical company and No. 1 in India. We provide high-quality, affordable medicines trusted by customers and patients in over 100 countries. Sun Pharma's global presence is supported by more than 40 manufacturing facilities spread across 5 continents, R&D centres across the globe, and a multicultural workforce comprising over 50 nationalities. Sun Pharma fosters excellence through innovation supported by strong R&D capabilities comprising around 3,000 scientists and R&D investments of over 6-8% of annual revenues. At Sun, our people are our greatest asset. Ours has never been a story of individual brilliance but of cultivating a culture of realising collective potential. In our journey, everyone is enabled to take charge in an environment that offers limitless growth opportunities. We are with you every step of the way, so you can shine for years to come. With the launch of our Employee Value Proposition (EVP), we define our promise to ‘Create Your Own Sunshine'—driven by the three pillars of Better Every Day, Take Charge, and Thrive Together. These pillars drive progress at Sun so that people can achieve what they would have thought impossible. Learn more about our EVP here: https://sunpharma.com/careers/

LinkedIn followers
2,343,928
People associated on LinkedIn
47,337
Reported office locations
  • Sun House, CTS No. 201 B/1,, Western Express Highway, Goregaon East, Mumbai, Maharastra 400063, IN
Business categories
  • Biotechnology
  • Manufacturing
  • Pharmaceutical
Other recorded names
  • Sun Pharmaceutical Industries Ltd
  • SUN PHARMA
Specialties
  • Formulations
  • API
  • US Generics
  • Speciality brands
  • and Technically complex formulations
Profile identifies a recruitment agency
No
Reported total investment
0

Currency and observation date were not supplied; this is not a current valuation or a funding round.

Sun Pharma is the world's fourth-largest speciality generic pharmaceutical company and No. 1 in India. We provide high-quality, affordable medicines trusted by customers and patients in over 100 countries. Sun Pharma's global presence is supported by more than 40 manufacturing facilities spread across 5 continents, R&D centres across the globe, and a multicultural workforce comprising over 50 nationalities. Sun…

FieldValue
IndustryPharmaceutical Manufacturing
Company size10,001+ employees
HeadquartersMumbai, Maharastra
Organization typePublic Company
Year founded1983
SpecialtiesFormulationsAPIUS GenericsSpeciality brandsand Technically complex formulations
Open jobs on Jobsy26
LinkedInView page
Job description

Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients.

As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being.

Reaching People. Touching Lives.

Job purpose

Specialist, Quality (Investigations) is responsible for ensuring products are manufactured, inspected, tested and packaged according to GMP and Company requirements. This is done on a day-by-day basis by the ensuring deviations investigations are managed in compliance with Sun Pharma Global Quality Standards, GSOPs, SOPs and Regulatory requirements through the identification of the root cause, assessment of the associated risks and establishment of the effective CAPAs.

Duties and responsibilities

  • Prepares deviation investigation reports
  • Ensure identification of the root cause of the issue and execute risk assessments based on the findings of the investigation
  • Ensures that all activities related to the recognition, investigation and resolution of non-conformities are performed in a timely manner and in compliance with the company and regulatory requirements
  • Obtain and maintain current Lead Investigator and Approver certification status as per the Certification Program requirements
  • Ensure appointment of the Subject Matter Experts (SMEs) from relevant areas and their participation in the investigation’s execution and Board discussions
  • Support all activities associated with Investigator and Approver Certification Program
  • Manage TrackWise access and system training of the site personnel involved in the investigations based on their training and certification status
  • Ensure assessment of the CAPAs effectiveness and timely execution of all the associated actions
  • Identify relevant regulatory requirements for non-conformance investigations and ensure their implementation in the facility
  • Work with other departments to proactively build quality into the processes and systems
  • Develops or assists with Change Controls and SOP's as required
  • Participate in Internal, Customer and Regulatory Audits
  • Other duties as assigned

Additional responsibility (Only applicable to customer facing roles)

Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day

Qualifications

  • Bachelor's Degree in Science, or related discipline
  • Minimum 1 Year experience in a Quality Assurance, Quality Control or Manufacturing experience role within the pharmaceutical industry preferably in handling non-conformance investigations.
  • Good working knowledge of pharmaceutical Quality Systems.
  • Experience in coordinating team activities
  • Experience in dealing directly with Regulatory Agency officials (Health Canada and FDA)
  • Knowledge of pharmaceutical standards, transfer guidelines, validation requirements
  • Strong focus on flexibility, ability to multi-task, attention to detail, excellent organizational skills, good follow-up, excellent communication and writing skills
  • Experience in Quality electronic systems such as Trackwise, Learning Management System (LMS), Electronic Documentation Management System (EDMS), and SAP is an asset

Working conditions

  • Non-routine and complex problems
  • Dealing interdepartmentally/across sites to attempt to obtain facts in a rapidly changing atmosphere
  • Ability to work under stressful conditions and prioritize workload
  • Numerous and varied responsibilities demanding attention and detail

Physical requirements

  • Office based role
  • Regular hours are 8:00am to 4:30pm with extended hours as required to resolve urgent issues

This posting is for an existing vacancy.

The presently-anticipated base compensation pay range for this position is $63,500 to $79,500. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; RRSP savings plan; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.

The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, ethnic origin, citizenship, ancestry, sex, age, marital status, family status, physical or mental disability, gender identity, gender expression or any other ground protected by applicable human rights legislation.

The Company uses artificial intelligence to screen, assess or select applicants.

Notice to Agency and Search Firm Representatives: Sun Pharmaceuticals Industries, Inc. (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. 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.

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