IPC Specialist - New Capital

The In-Process Quality Specialist is responsible for executing and monitoring all in-process quality

controls during manufacturing operations to ensure product quality, compliance with cGMP

activities which directly or indirectly impact the quality of the product manufactured in GEPD New

Capital Manufacturing site.

Environment

Internal and external interactions i.e.: with other departments/divisions, international scope,

providers, customers)

Internal: GEPD Manufacturing site teams, Quality System Team, Operations, and other

supportive functions.

External: In absence of the In-Process Quality Manager, Auditors and Health Authorities.

Key responsibility

Perform in-process checks, sampling, and testing in accordance with approved procedures and

regulatory guidelines.

Ensure proper use, handling, cleaning, and segregation of sampling equipment to prevent

cross-contamination.

Conduct regular GEMBA and shop-floor walkthroughs to verify compliance with GMP,

GEPD, and IPC requirements.

Review and verify IPC records, batch data, critical parameters, and equipment logs for

accuracy and compliance.

Support the implementation and maintenance of the Contamination Control Strategy (CCS)

by following defined controls, identifying gaps, and reporting risks related to contamination

prevention.

Ensure timely and accurate IPC documentation and support batch record completion to enable

batch release readiness.

Monitor IPC results, identify deviations, atypical events, or trends, and escalate further

investigation.

Support implementation and improvement of IPC procedures and cross-contamination control

practices (cleaning, validation, and use of dedicated or disposable equipment).

Coordinate with production to ensure adherence to IPC frequencies and availability of required

materials and equipment.

Academic experience required

Bachelor's degree in health-related Sciences, preferably as a pharmacist.

Knowledge of cGMP requirements, aseptic processing and in-process Quality Control.

Professional experience required

Minimum 2-3 years of experience in similar position at GMP pharmaceutical manufacturing,

with aseptic operations.

Computing skills

Proficiency in computer, MS Office knowledge.

Experience with eQMS and ERP systems.

Personal skills
Organized and able to manage time effectively.
Ability to work within a highly regulated, labor-intensive environment.
Ability to understand, explain, follow, and enforce SOPs.
Organizational and problem-solving skills.
Strong integrity and commitment to Quality and Compliance.
Ability to work in groups and with other departments.
Excellent oral and written communication skills to produce clear and concise factual findings.