You

Profile
Goals

Community

People

Pay & Market Info

Roles
Employers
Qualifications

Job Search

Jobs

Preferences

CurrencyUSD

Support

About
Feedback
Help

← Back to jobs

BranchFactor

You

Profile
Goals

Community

People

Pay & Market Info

Roles
Employers
Qualifications

Job Search

Jobs

Preferences

CurrencyUSD

Support

About
Feedback
Help

← Back to jobs

Quality Compliance Specialist at Eva Pharma — BranchFactor

← Back to jobs

Apply →

Quality Compliance Specialist

Eva Pharma · Giza · Full-time

Posted 31 Aug 2025

Advertised as “Quality Compliance Senior Specialist”

Apply →

BranchFactor Summary

The original posting with the fluff stripped out

Expected experience: 2–4 yrs
Management level: Individual contributor
Contract: Full-time

Compensation

No salary listed for this role.

Role speciality

Pharmaceutical Quality ManagementQuality Compliance

Useful technologies

ExcelMicrosoft OfficeMS OutlookPowerPointWord

Original posting

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

More openings like this

Quality Compliance SpecialistHims & Hers · US RemoteUSD 90K–115K Quality Compliance SpecialistStanley 1913 · Ho Chi Minh City Quality Compliance SpecialistJASARA PMC · Riyadh, Riyadh Province, Saudi Arabia Contracts LawyerEva Pharma · Giza, Al Qāhirah, Egypt See all Legal & Compliance openings →

Job Summary

We are seeking a passionate and talented Quality Compliance Senior Specialist / Supervisor to join our dynamic team.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities

Handling of deviations according to the current procedure including initial assessment, root cause investigation, root cause identification, and proposal of corrective & preventive actions.
Handling of changes within the site according to Change Management SOP along with the associated follow up of actions.
Implement Product Quality Review procedure and follow up of QMS CAPA closure and effectiveness check.

Requirements

Bachelor’s degree in Pharmaceutical Sciences.
2-4 years of experience in a similar position with proven track record in passing regulatory inspections.
Excellent communication and interpersonal skills, Result-oriented personality with team working ability & resilience.
Fluency in spoken & written English is required, Excellent knowledge of Microsoft Office Professional (word, Excel, PowerPoint, MS Outlook).

More openings like this

Sourced from workable · original listing