Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.
Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. Your knowledge of quality control will be helpful to support our quality programs.
Your ability to maintainance the reference substances, biotechnological reference standards, reagents and columns stock, will help us manage our quality.
Your contribution to maintain the stock in the laboratory will help Pfizer provide safe drugs to its patients.
Your qualifications of unique Quality Control instruments will help us meet accuracy specifications for sample management, retains managements, interpretation and evaluation.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Assist in assortment of standards, download standards in database, expiration review, notification of standards to expire, update of standards database.
Assist in inventory of biotechnological standards, logistics for sending biotechnological standards to third party.
Assist in Reagents and consumables reception, reagents reception log record, new entries in the reagents and consumables database.
Assit in column reception, entry of new entries in column database, discharge of used columns, update of column database
Manage receipt, storage and handling of reference standards, reagents and columns.
Ensure all documentations are conducted in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance to existing policies.
Review and revise Standard Operating Procedures (SOPs) to keep them current.
Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Demonstrated technical skills in manage stocks and inventory database
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
Laboratory work experience with analytical HPLC (High Pressure Liquid Chromotography) technique
Experience leading continuous improvement projects
Knowledge of lean manufacturing, six sigma methodologies, and statistics
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control