Job Description

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.


Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

:

As a member of the Microbiology Quality Control team, you will be responsible for conducting a range of microbiological tests to ensure compliance with regulatory and internal quality standards. Your key responsibilities will include:


#

Microbiological Testing & Analysis:

Perform testing of

sterile samples

including Sterility, LBPC (Limulus-Based Pyrogen Test), and BET (Bacterial Endotoxin Test)with proper documentation. Conduct testing of

non-sterile samples

, such as Microbial Limit Test (MLT) and Bioburden*, along with accurate record-keeping.
Perform

microbiology assay testing

and document results in compliance with GMP. Carry out

microbiology culture testing

including maintenance, sub-culturing, Growth Promotion Testing (GPT), and microbial identification.
#

Water & Environmental Testing:

Perform

water testing

, release analysis, and related documentation. Conduct

environmental monitoring

in classified areas across Julphar production plants and microbiology labs, ensuring accurate and timely documentation.
#

Lab Support Activities:

Execute various

microbiology lab support activities

including equipment monitoring, cleaning validations, and media preparation. Monitor equipment and area temperatures using

Vaisala/SIRIUS systems

. Ensure real-time documentation and compliance for all assigned tasks. Handle

sample and result entries

, reservation creation, and notification processes in

SAP

.
#

Compliance & Documentation:

Adhere strictly to

Good Laboratory Practices (GLP)

,

Data Integrity

, and

Good Documentation Practices (GDP)

. Prepare and review

Standard Operating Procedures (SOPs)

and support microbiology-related

qualification/validation documentation

. Participate in

internal and external audits

and promptly report any deviations, OOS (Out of Specification), OOL (Out of Limit), or excursions. Manage documentation and deviation handling through

eQMS (Amplelogic system)

.
#

Safety & Best Practices:

Follow all

safety protocols

and ensure a clean and compliant laboratory environment. Ensure full compliance with company policies, GMP, and regulatory guidelines.

Core Competencies:

Strong sense of

accountability and ownership

Highly

disciplined, motivated, and well-organized

Excellent

process compliance

and

implementation skills

Effective

time and task management

Proficient

English communication skills

(verbal and written)

Qualifications & Functional Knowledge:

Bachelor's or Master's Degree in

Microbiology

or other

Biological Sciences

4-6 years of relevant experience

in a pharmaceutical microbiology lab (preferably in sterile and non-sterile product testing) Proficient in computer applications including

MS Word, Excel, and PowerPoint

Familiarity with

SAP

,

eQMS (Amplelogic)

, and

temperature monitoring systems

like Vaisala/SIRIUS is a plus
We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar