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Summer Student, Quality Control

0-1 years
Not Disclosed
10 Jan. 28, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Here's a revised version of the job description in a professional and clear format:


Job Title: Summer Student, Quality Control
Location: Kirkland, QC
Position Type: Full-time Summer Internship (37.5 hours per week)
Salary: Competitive hourly wage (to be discussed during the interview)

About Jubilant Radiopharma:
Jubilant Radiopharma is a leader in the radiopharmaceutical industry, committed to delivering high-quality products that make a real impact on patients' lives. We offer more than just a job; we provide a platform for professional growth in a collaborative and supportive environment. This summer, we invite you to join our Quality Control (QC) department and contribute to our mission.

Position Overview:
As a Summer Student in Quality Control, you will gain hands-on experience in document management, training support, performance tracking, and regulatory inspection preparation. This is a great opportunity for students pursuing a scientific degree to apply their knowledge in a dynamic work environment.

Key Responsibilities:

  • Document Management:
    Assist the QC team in organizing, filing, and archiving GMP (Good Manufacturing Practice) documents, ensuring everything is properly stored and easily accessible.

  • Record Distribution:
    Distribute records to the appropriate departments efficiently, ensuring proper communication and record-keeping across the team.

  • Training Support:
    Contribute to the revision and improvement of training materials, supporting the continuous enhancement of our educational programs.

  • KPI Reporting:
    Help generate weekly KPI (Key Performance Indicator) reports, providing insights into performance metrics and contributing to data-driven decision-making.

  • Learning Plan Development:
    Participate in the creation of new learning plans that foster a culture of continuous improvement and development.

  • Inspection & Audit Support:
    Assist with preparation for regulatory inspections and audits, ensuring compliance and readiness.

Qualifications & Skills:

  • Educational Background:
    Currently pursuing a Bachelor’s degree in Science (e.g., Biology, Chemistry, or related field) and returning to your studies in Fall 2025.

  • Language Proficiency:
    Bilingual in English and French (spoken and written).

  • Technical Skills:
    Proficient in the Microsoft Office Suite (Word, Excel, PowerPoint) and familiar with SAP or similar software platforms for document management.

  • Attention to Detail:
    Exceptional attention to detail, strong organizational skills, and effective time management to ensure that projects stay on track and deadlines are met.

  • Availability:
    Available for a full-time position (37.5 hours per week) at our Kirkland, QC location for the duration of the summer.

What We Offer:

  • Hands-On Experience:
    Gain practical experience in Quality Control, directly contributing to key processes that ensure product quality.

  • Professional Exposure:
    Work closely with senior management and various departments, gaining visibility and building a professional network.

  • Career Development:
    Develop valuable skills in document management, process improvement, and regulatory compliance that will serve as a strong foundation for your future career.

Application Deadline:
All applications must be submitted by February 9, 2025.


How to Apply:
Click on the "Apply Now" button to submit your resume and cover letter.