Pfizer Pharma jobs – QC openings for pharmacy and chemistry graduates
Pfizer fresher and experienced quality control job openings for chemistry and pharmacy graduates
Pfizer is a pharmaceutical company that employs quality control professionals to ensure that the products it manufactures meet the necessary quality standards. Quality control jobs at Pfizer may involve testing raw materials and finished products, conducting inspections, and maintaining documentation to ensure compliance with regulations. These professionals may also be responsible for troubleshooting problems with products and identifying ways to improve the quality of products. In order to work in quality control at Pfizer, you may need to have a degree in a field such as chemistry, Pharmacy
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 analyze chemical, biological or microbiological products will help us manage our quality. Your contribution to analytical testing will help Pfizer provide safe drugs to its patients.
Your qualifications in unique Quality Control instruments will help us meet accuracy specifications for sample management, retains management, interpretation, and evaluation. You will also be relied on for establishing requirements for the transfer of methodology from R&D.
As an associate, your focus on the job will contribute to 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.
Pfizer QC Job description
- Assist in the preparation of media, maintenance of dehydrated and prepared media stocks, and sterilization of media accessories by autoclave cycles.
- Ensure training records are updated and correctly filed to reflect current testing capabilities.
- Perform sampling and labeling of materials as per defined procedure and verification of all the equipment/instruments.
- Interpret and evaluate data in terms of accuracy, precision, trends, and potential Good Manufacturing Practices {also cGMP} impact and recommend appropriate corrective actions.
- Ensure all documentation and quality records are conducted in accordance with Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance with existing policies.
- Review and revise Standard Operating Procedures (SOPs), analytical methods, and related procedures/documents, to keep them current.
- Perform analyses on finished products, raw materials, and components including entry, review, and/or approval of data in a computerized database and generate EMS reports.
- 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.
Qualifications
- Bachelor’s Degree in Pharmacy or Master’s in Chemistry/ Pharmacy.
- 0-5 years of experience in Quality Control.
- Demonstrated technical skills in analytical 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.
SKILLS
- Laboratory work experience with analytical HPLC (High-Pressure Liquid Chromatography) technique
- Experience leading continuous improvement projects
- Knowledge of lean manufacturing, six sigma methodologies, and statistics.
Work Location Assignment: On-Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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