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.

Job Summary / Main Purpose

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The

Quality Control (QC) Manager

at Julphar HQ is a strategic leadership role responsible for managing the overall Quality Control operations, ensuring adherence to regulatory standards (GMP/GLP) and internal quality policies. The role oversees both

Chemical and Microbial laboratories

, ensuring all materials and products meet approved specifications, regulatory requirements, and internal standards of excellence.



The QC Manager is responsible for managing ongoing commercial stability programs, regulatory compliance, laboratory operations, documentation, and investigations. This role plays a critical part in maintaining

product quality, safety, and data integrity

, and contributes to the continuous improvement of quality systems and cross-functional collaboration.

Key Responsibilities

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Ensure the quality of

raw materials, packaging materials, and finished products

is in strict compliance with approved specifications and GMP/GLP standards. Lead, manage, and oversee operations in both the

Chemical and Microbial QC laboratories

, ensuring timely and accurate testing in accordance with protocols, GMP, and safety regulations. Oversee and execute

commercial stability programs (ongoing/commitment)

in compliance with regulatory expectations. Review and approve

SOPs, protocols, and reports

(including method validation, method transfers, process validation, and stability studies). Approve

chemical and microbiological analysis reports

and analytical batch records. Ensure

timely completion and closure

of investigations (OOS, OOT, deviations) in compliance with SOPs and regulatory expectations. Lead and manage all

laboratory investigations

, implementing appropriate CAPAs. Ensure

data integrity

compliance in all QC processes, as per current regulatory and company protocols. Update procedures and quality practices to remain aligned with evolving

cGMP and regulatory guidelines

. Provide technical support to internal and external audits and ensure effective

closure of audit observations

. Support

cross-functional departments

(R&D, Regulatory Affairs, Production, Compliance, etc.) in achieving organizational objectives. Manage quality systems within the QC department including

Change Controls, Deviations, CAPAs, and Self-Inspections

, using the

AmpleLogic EQMS

system. Oversee

training and development

of QC staff; conduct onboarding and continuous training to ensure competency and compliance. Participate in the

preparation of department budgets

and monitor resource allocation and spending. Continuously analyze and improve QC processes to increase operational efficiency, reduce errors, and enhance product quality. Ensure full

adherence to cGMP practices

and promote a strong culture of quality and compliance.

Core Competencies

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Leadership & Collaboration

Proven leadership skills with the ability to manage multi-disciplinary teams and collaborate with cross-functional departments to align on quality goals.

Strategic Thinking & Quality Culture

Strong analytical and strategic mindset, with the ability to influence and drive transformation of quality culture at the organizational level.

Decision-Making & Problem-Solving

Solution-oriented with the ability to make sound scientific and compliance-based decisions under pressure.

Project & Performance Management

Experienced in managing multiple priorities, delivering results, and driving continuous improvement initiatives.

Technical & Regulatory Expertise

In-depth understanding of regulatory guidelines (e.g., GMP, GLP), data integrity principles, and audit readiness, with strong documentation and reporting skills.

Communication & Interpersonal Skills

Excellent verbal and written communication skills with strong interpersonal abilities to effectively engage with stakeholders at all levels.

Qualifications & Experience

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Education:

Bachelor's degree in Pharmacy (Master's preferred).

Experience:

Minimum of 10 years in Quality Control within the pharmaceutical industry, with at least 3-5 years in a managerial or leadership role.

Regulatory Knowledge:

Deep understanding of cGMP, GLP, ICH guidelines, and other applicable regulatory requirements.

Systems & Tools:

Experience with EQMS systems (e.g., AmpleLogic), SAP, and data integrity practices.

Leadership:

Proven ability to manage complex, cross-functional teams and resolve operational challenges.

Audit Experience:

Hands-on experience with regulatory inspections and implementing effective post-audit action plans.

Preferred Certifications & Skills

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Lean Six Sigma or equivalent quality/process improvement certification (preferred). Training in data integrity, regulatory inspection management, and risk-based quality systems. Strong business acumen and cost-conscious mindset.
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