Quality Control Analyst

Posted 3 Days Ago
Be an Early Applicant
Cairo
Junior
Healthtech • Biotech • Pharmaceutical
The Role
The Quality Control Analyst conducts various testing and analysis in a laboratory setting, ensuring quality control through documentation, data integrity, and compliance with regulations. Responsibilities include method validation, data interpretation, managing laboratory instruments, and supporting regulatory submissions. This role requires attention to detail and the ability to work independently and in teams.
Summary Generated by Built In

Viatris Egypt S.A.E

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via: 
Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and 
Partnership – Leveraging our collective expertise to connect people to products and services. 
 

Every day, we rise to the challenge to make a difference, and here’s how the Quality Control Analyst (Stability and Methodology) role will make an impact:

  • Position summary:
  • Conduct routine and non-routine analysis and relevant documentation and reporting.
  • Performance of lab-related tasks.

Job Specific technical/Functional/Professional Competencies:

  • Conduct stability & method validation testing and the corresponding documentation to support the timely disposition of product.
  • Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.
  • Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms.
  • Write technical reports or prepare graphs or charts to document experimental results.
  • Participate in out-of-specification and failure investigations and recommend corrective actions.
  • Supply quality control data necessary for regulatory submissions.
  • Investigate or report questionable test results.
  • Manage stability chambers.
  • Execute all activities related to process, cleaning, and instrument validation.
  • Prepare and execute the SOPs, calibration, and validation documents (IQ, OQ & PQ) related to chemical laboratory tasks.
  • Using, monitoring, and controlling of laboratory chemical reagents inventory and expiry
  • Perform Data loggers monitoring, downloading, and reviewing.
  • Work on improving his/her process by implementing lean and 6σ projects.
  • Ensure that all results generated follow data integrity requirements and following ALCOA principles all over operations.
  • Comply with all Viatris Quality Standards and procedures.
  • Knowledgeable with basic Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.
  • Raise “NTM” Notification to Management whenever condition in Viatris policies applies.
  • Support Supply department by sending stability samples on time, evaluation of stability results and taking any immediate actions required in addition to archive of these results for toll manufacturing products.
  • Create/review of stability schedule, protocols, reports, and trends.
  • Follow up stability equipment calibration & maintenance and ensure appropriate documentation and archiving.
  • Maintain laboratory supplies inventory required for Stability analysis.
  • Handle the global changes affecting stability and methodology.
  • Support QA with all CCRs and QARs related to Stability & Methodology.
  • Perform all method validation activities required.
  • Create/review of method validation protocols and reports.

Experience and Knowledge

  • Good command of English in both written and spoken.
  • Excellent in Microsoft office (word, excel & PowerPoint)
  • Knowledgeable with interpersonal, good communication and presentation skills.
  • cGMP & cGLP knowledge is preferred with particular emphasis on Quality Control.
  • Knowledgeable with Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.

Essential Personal Qualifications

  • Bachelor’s degree in pharmacy or science.
  • 1-5 years’ experience in a related area.
  • Demonstrated ability to work independently.
  • Excellent documentation and technical writing skills.
  • Able to work in a team, interact with various priorities and meet deadlines.
  • Active, organized and planner with high attention to details.
  • High observation skills.
  • Self-motivated and able to consistently meet timelines.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. 

Viatris is an Equal Opportunity Employer.

The Company
HQ: Canonsburg, PA
16,557 Employees
On-site Workplace

What We Do

Viatris is a global pharmaceutical company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer.

Similar Jobs

Cairo, EGY
9 Employees

Pixelogic Media Logo Pixelogic Media

Continuous Improvement Manager

Digital Media • News + Entertainment
Cairo, EGY
2002 Employees
Cairo, EGY
26878 Employees

Foodics Logo Foodics

Head of COE Outsourced Site - Customer Operations

Fintech • Food • Payments • Financial Services
Cairo, EGY
853 Employees

Similar Companies Hiring

AcuityMD Thumbnail
Software • Healthtech
Boston, MA
168 Employees
Zealthy Thumbnail
Telehealth • Social Impact • Pharmaceutical • Healthtech
New York City, NY
13 Employees
Cencora Thumbnail
Pharmaceutical • Logistics • Healthtech
Conshohocken, PA
46000 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account