pfizer asia pacific pte ltd Jobs & Career

Job Description : Why Patients Need You Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the med

Job Description : As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Clinical Data Scientist (CDS) is responsible for timely and high-quality

Job Description : Why Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether y

Job Description : APPOINTMENT The appointment of Professional Service Officer is in the Executive Cadre of the Company and reflects the importance of the incumbent’s role as an important and active link between the Company and its customers in estab

Job Description : Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory env

Job Description : * Liaise withSite / Corporate Quality function to represent Vizag site for Global procedural improvements. * Manage investigations and apply relevant and necessary actions/ systems to ensure appropriate levels of compliance.

Job Description : >> Perform filing and ensure compliance of monthly, quarterly, half yearly and yearly returns under GST >> Perform review of general ledgers for GST balances and reconciliation with returns on monthly basis >> Review transnational

Job Description : MAIN REPONSIBILITIES / DUTIES Responsible for providing support to the Pfizer Biopharmaceuticals Group (PBG),Vaccines Business Unit, Global Medical Affairs team specifically: * Develop abstracts, posters, manuscripts, congress p

Job Description : ROLE SUMMARYAs part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Associate Data Manager is responsible for timely and high quality

Job Description : Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory env

Job Description : Qualifications Must-Have * Masters Degree (Microbiology) with 0-2 years of Experience in pharmaceutical industry * Demonstrated technical skills in water sampling and analysis * Microbiology best laboratory practices * A

Job Description : Target years of experience: 4-7 yrs of Instrumentation experience for Diploma engineers/Graduate engineers in maintenance function of pharmaceuticals industry Technical Skills: • Knowledge on operation and maintenance of respective

Job Description : ROLE SUMMARYAs part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Senior Associate, Lab Data Specialist is responsible for man

Job Description : This role will support the Logistics Center Quality Director in daily activities related to quality logistics within the Intercompany Organization. This role is responsible to ensure the continuity of daily operations linked to sup

Job Description : She will be responsible for meeting HCPs and achieving Budgets. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Sales#LI-PF

Job Description : Position of Govt. KAM at Kolkata, KAM will be exclusively looking after Govt. Accounts of the assigned geographical area. He will be ensuring below mentioned key actions. * Coverage of Kay Accounts in the assigned territory. * Deve

Job Description : Why Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether y

Job Description : Position Purpose To oversee and direct regional/national submission portfolio execution associated with 40,000 submissions worldwide to regulatory health authorities per annum, through leadership and engagement of Hub Submission M

Job Description : Why Patients Need You Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their r

Job Description : * Theoretical & practical knowledge on working principle of analytical instruments- FTIR, UV, IR, HPLC, GC with minimum 5 years of relevant experience * Understanding on the purpose of different method validation parameters an

Job Description : ROLE SUMMARY * Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. * Provide statistical expertise and contrib

Skills : Manager , biostatistics

Job Description : ROLE SUMMARY This position will provide statistical support for clinical Phase I-IV projects in Vaccine Research and Development. The successful candidate will collaborate with study teams working effectively to design studies, dev

Skills : Sr. Manager , biostatistics

Job Description : * Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations. * Maintain regulatory compliance in accordance with cGMP practices * Ensure manufacturing

Job Description : * ROLE SUMMARY As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Senior Associate Data Manager is responsible fo

Job Description : * Functions as Regulatory support for Biosimilars development projects and the lifecycle changes, works with Global Product Owners (GPOs), cross functional teams, local and regional regulatory colleagues, external partners (in ca