Pfizer Limited Walk-in Interview 2023.Pfizer Limited 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: Associate Manager – MSAT – Women only
- Qualification: B.Pharma in Any Specialization, B.Tech/B.E. in Chemical
- Experienced:7 – 12 years
Job Description: Greeting from Pfizer Limited !!!!
Important Details :
- Post of date:06/02/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To face Interview
- Interview Rounds of Interview: HR
Roles and Responsibilities
- Responsible for executing the end-to-end technology transfer activities of new product introduction of Sterile injectables.
- Maintain a contemporary awareness of Global Business Practices, methods, specifications, Standard Operating Procedures, Pharmacopoeial trends, International Conference on Harmonization guidelines and regulatory expectations.
- Work closely with process experts and project teams to provide timely support for formulators in the form of quality data which can be used in support of regulatory documentation of new drug applications.
- Independently carry out all aspects of practical work necessary to provide right first time results.
- Responsible for performing feasibility studies, MOC studies, dwell time studies and lab scale batches as part of technology transfer activities.
- Responsible for performing Engineering batches, scaleup batches, and Exhibit batches as part of technology transfer activities.
- Attend project team and brainstorming meetings and present data.
- Responsible for providing the required data for regulatory submissions.
- Experience with technology transfer activities or formulation development of Sterile injectables.
- Ability to extract relevant information from scientific literature, accurately record observations, facts, data and conclusions during studies or Good Manufacturing Practices {also cGMP} investigations
- Interact effectively with peers and leaders as part of a multi-disciplinary team
- Effective verbal and written communication skills
- Experience in a {Current} Good Manufacturing Practices {part of GxP} laboratory
- Understanding of various scientific software or software used in pharmaceutical or production environment
- Desire to develop their own technical skill set is essential.
Please share resume to zabiulla.m@pfizer.com
