Quality Control Analyst - Contract

Pfizer, S.A. de C.V; Saudi Arabia; On-site; SAR 168,000 - 244,000; Full time

Job summary

A global pharmaceutical company in Saudi Arabia is seeking a qualified candidate to assist in media preparation and carry out microbiological tests. This role requires strong technical skills and the ability to multi-task in a fast-paced environment. Ideal candidates should have a Bachelor's degree or equivalent experience and be proficient with Quality Control instruments. Join our commitment to delivering high-quality products to patients worldwide.

Benefits

Competitive compensation and benefits

Innovative work environment

Qualifications

• Ability to understand compendial methods and governmental regulations.
• Proficiency with Quality Control instruments for sample management.
• Knowledge of Good Manufacturing Practices and their application.

Responsibilities

• Assist in preparation and maintenance of media stocks.
• Perform microbiological tests and ensure compliance with Good Manufacturing Practices.
• Conduct analyses on finished products and maintain quality records.

Skills

Technical skills in method validation and testing

Strong written and verbal communication skills

Excellent organizational skills

Ability to multi-task

Education

Bachelor's degree

Associate's degree with 4 years experience

High school diploma with 6 years experience

Tools

Analytical HPLC techniques

Quality Control instruments

Job description

Overview

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

Responsibilities

What You Will Achieve

• Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.
• Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.
• Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.
• Ensure training records are updated and correctly filed to reflect current testing capabilities.
• Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.
• Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
• Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
• Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
• Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.
• Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.

Minimum Requirements

• Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
• Demonstrated technical skills in method validation and testing
• Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
• Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
• Excellent organizational skills and strong ability to multi-task
• Strong written and verbal communication skills
• Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Preferred Qualifications

• Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques
• Proven track record in leading continuous improvement projects
• Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
• Strong problem-solving skills and attention to detail
• Ability to manage multiple priorities and meet deadlines.
• Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
• Adaptability and willingness to learn new techniques and procedures

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.