Pfizer Walk In Interview 2023.Pfizer Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue. Life, it is the underlying purpose of everything we do at Pfizer. A purpose that defines our R & D strategy of discovering and developing innovative products that improve the quality of life. The worlds number one healthcare company, we have an annual turnover exceeding US $ 54 Billion and an annual global R & D spend of over US $ 7 Billion.
Vacancy details:
- Post Name: Quality Control – Microbiology /Equipment Maintenance Engineer/Instrumentation Engineer/HVAC Engineer- Women only
- Qualification –MS/M.Sc(Science) in Microbiology/B.Tech/B.E. in Mechanical/B.Tech/B.E. in Instrumentation
- Experienced: 2-7 years of experience
- Contact – Pfizer HR Team
Job Description: Greeting from Pfizer !!!!
Important Details :
- Location: Visakhapatnam
- Post of date:02/03/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Quality Control – Microbiology – Women only
Roles and Responsibilities
- Assist in preparation of media, maintenance of dehydrated and prepared media stocks, and sterilization of media accessories by autoclave cycles.
- Assist in maintenance of Master cultures Isolates and preparation of Cryo vials.
- Manage receipt, storage and handling of Bio ball cultures.
- Perform water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test and Assays, 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 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 documentations and quality records 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), 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.
- Conduct Microbiological protocols on an as needed basis.
- 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 Media Preparation, GPT 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
- Laboratory work experience with Microbiological techniques
- Experience leading continuous improvement projects
- Knowledge of lean manufacturing, six sigma methodologies, and statistics
Please send resume to zabiulla.m@pfizer.com
Equipment Maintenance Engineer – Women only
- Contribute to the completion of project milestones and organize own work to meet project task deadlines.
- Support Engineering team in planning and overseeing the preventative maintenance for filling equipment.
- Manage the status of work control and backlog for work order submission to work order completion.
- Support maintenance work management and the installation, commissioning, qualification of equipment.
- Contribute to continuous process improvements initiatives.
- Provide input to capital project design with respect to equipment selection and specifications that create project approaches which minimize life cycle costs.
- Follow up and communicates schedule to all resources, i.e. maintenance, production, outside services, stores and engineering.
- Responsible for pest control management in compliance with Good Manufacturing Practices (also cGMP) and Pfizer internal requirement.
- Manage all the utility document and drawings and ensure all of them are sorted and archived properly.
- Ensure that supporting Good Manufacturing Practices (also cGMP) relevant documentation is generated and maintained.
- Documentation/Compliance
- Executing activities complying with cGMP, Quality and safety procedures and practices
- Initiating, tracking and closing of Change controls, Incidents, CAPAs and Effectiveness Checks.
- Coordination during the Walkthroughs, Internal Audits / Regulatory Audits
- Logbooks Management
- Preparation and Review of respective Documents / Procedures
- Coordinate for Engineering PQS Implementation
- Ensuring on track of the Change Controls, Incidents, CAPAs and Effectiveness Checks
- Coordinating with cross functional teams for closing of the actions
- Preparation of drawings as per site requirementsStatutory Obligation
- Conduct himself/herself in line with relevant legislation pertaining to workplace health and safety, discrimination, harassment and bullying.
- Participate in and take responsibility for workplace environment, health and safety at the level required for this position, following the guidelines in the company Environmental, Health and Safety Management System Manual.
- Ensure plant and personnel safety
- Ensuring that health and safety guidelines are strictly followed
- Environmental Health and Safety
- Well versed with Microsoft word, Auto CAD and excel
- Knowledge of Track wise software
- Preparation of drawings/layouts (Civil, Engineering drawings etc)
Please send resume to zabiulla.m@pfizer.com
Instrumentation Engineer – Women only
Technical Skills:
- Knowledge on operation and maintenance of respective utility / equipment / system
- Knowledge of preventive and breakdown maintenance
- Troubleshooting of Hardware/Software issues; VFD configuration; PLC basic programming and hardware troubleshooting knowledge
- Should have the process instrumentation knowledge and different type of Automation system communication protocols
- Should be conversant with Validation Documents, Preventive Maintenance
- Schedules/Check sheets, SOPs & Various Audit Procedures
- Should have Knowledge on Installation and Maintenance of Filling Lines (Washing, Tunnel, Filling, Capping) and solution preparation equipment
- Knowledge on qualification program FAT / SAT /DQ / IQ / OQ / PQ
- Standards, Processes & Policies:
• Knowledge on metrological standards
• Standard instruments
• Global calibration policies
• Knowledge on Clean room requirements and Regulatory Guidelines
Responsibilities:
- Prepare specifications for process equipment
- Prepare and maintain engineering drawings
- Prepare Equipment installation drawings and ensure the installation of the equipment as per the same
- Review drawings issued by vendor.
- Complete periodic inspections of the vendors site to check for the progress of manufacturing of the equipment
- Plan and execute preventive maintenance program
- Attend to breakdowns, troubleshoot and rectify basic issues in shortest possible time
- Ensure that all safety instructions and measures are strictly observed
- Study and review standby facilities for critical sub-assemblies and addition of capital equipment on long term basis for smooth operation
- Prepare monthly reports
- Preparation and Review of respective Documents / Procedures
Please share resume to zabiulla.m@pfizer.com
HVAC Engineer – Women only
Roles and Responsibilities
- Knowledge of Installation, Operation and Maintenance of Centralized HVAC System Air Handling units, Laminar flow stations, Building Management System, Environmental Monitoring System. Building Management System, TMS system extra
- Operation & Maintenance of Stability Chambers, Cold Chambers, Deep Freezers and related maintenance knowledge
- Conversant with Validation documents and schedule: FAT / SAT /DQ / IQ / OQ / PQ
- Knowledge in performing PRQ, PR Activities as part of validation.
- Experience in performing the HEAP Filter Integrity test, Air Velocity test extra i.e. Validation Tests
- Detailed knowledge of preventive maintenance schedules/check sheets, SOPs and various audit procedures
- Support maintenance work management and the installation, commissioning, qualification of equipment.
- Contribute to continuous process improvements initiatives.
- Follow up and communicates schedule to all resources, i.e. maintenance, production, outside services, stores and engineering.
- Manage all the HVAC document and drawings and ensure all of them are sorted and archived properly.
- Ensure that supporting Good Manufacturing Practices (also cGMP) relevant documentation is generated and maintained.
- Experience in reliability-based maintenance practices
- Demonstrated ability to write and provide simple and accurate instructions.
- Demonstrated computer and technical skills
- Knowledge or experience working in a Good Manufacturing Practices {also cGMP} environment
Please share resume to zabiulla.m@pfizer.com
