Químico Analista de Microbiología
Job Summary
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.
In this role you will:
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.
Bachelors degree with any years of experience or an Associates 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
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
Experience using common AI tools including generative technologies such as ChatGPT or Microsoft Copilot to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices including risk management and ethical use
OTHER JOB DETAILS
Last Date to Apply for Job: August 13th 2026
EEO (Equal Employment Opportunity) & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin or disability.
To learn more about acceptable and prohibited uses of AI during the recruitment process please review our candidate AI-use guidelines available onPfizer Careers.
Quality Assurance and ControlRequired Experience:
IC
About Company
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