Executive – Documentation (Quality Control) At High-Q Pharmaceuticals

Job Description

High-Q Pharmaceuticals is seeking a dedicated and detail-oriented professional for the position of Executive – Documentation (Quality Control) within their Quality Assurance department.

This role is crucial for maintaining the high standards of quality that the pharmaceutical industry demands. If you have experience in quality control, stability, and validation, and possess a Pharm-D or M.Sc. in Chemistry, this could be the perfect opportunity for you.

Role and Responsibilities

As the Executive – Documentation (Quality Control), your primary responsibility will be to ensure the accuracy, consistency, and compliance of all documentation related to quality control processes.

Your role will be vital in maintaining the integrity of the pharmaceutical products produced by High-Q Pharmaceuticals, ensuring they meet all regulatory standards.

Key Responsibilities:

• Documentation Management: Create, review, and manage documentation related to quality control processes, including stability studies and validation protocols.
• Compliance Assurance: Ensure that all documentation complies with industry regulations and company standards.
• Data Analysis and Reporting: Analyze quality control data and prepare reports that will be used for internal audits and regulatory submissions.
• Collaboration: Work closely with other departments, including Production, R&D, and Quality Assurance, to ensure the smooth flow of documentation and compliance with regulatory standards.
• Continuous Improvement: Identify areas for improvement within the documentation process and implement best practices to enhance efficiency and accuracy.

Departmental Role: Quality Control

The Quality Control department plays a critical role in the pharmaceutical industry, ensuring that all products meet the necessary standards before they reach consumers.

This department is responsible for testing raw materials, in-process materials, and finished products to ensure they meet the required specifications. As part of the Quality Control team, your work will directly impact the safety and effectiveness of the pharmaceutical products produced by High-Q Pharmaceuticals.

Typical Duties in Quality Control:

• Testing: Conducting rigorous testing of materials and products to ensure they meet specific standards.
• Stability Studies: Monitoring the stability of products over time to ensure they remain effective and safe for use.
• Validation: Validating processes and equipment to ensure they produce consistent and reliable results.

How You Can Contribute

In the role of Executive – Documentation (Quality Control), you will be at the forefront of ensuring that High-Q Pharmaceuticals maintains its reputation for producing high-quality, safe, and effective products.

Your attention to detail and commitment to compliance will be critical in upholding the standards that the pharmaceutical industry demands.

Ways to Make an Impact:

• Accuracy and Precision: Your ability to maintain accurate and detailed documentation will ensure that all quality control processes are thoroughly documented and compliant with regulations.
• Regulatory Compliance: By ensuring that all documentation meets industry standards, you will help the company avoid costly errors and potential regulatory issues.
• Collaboration: Your collaboration with other departments will be key to ensuring that all aspects of the quality control process are documented and executed correctly.