Associate scientist

Posted 12 Hours Ago
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Chennai, Tamil Nadu
Hybrid
Junior
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
The Associate Scientist is responsible for analytical method development, validation, and routine analytical studies for APIs, intermediates, and different drug product formulations. This role involves adhering to GxP standards, ensuring compliance with quality and safety regulations, and coordinating with cross-functional teams to meet project milestones.
Summary Generated by Built In

Department Name
AT-GTE, Chennai
Job Title
Associate Scientist (Chem Analytical)
Global Job levels
Job Family Group: Research and Development
Job Family: 093- Chemistry-Analytical
Job Category: Research
Job Level: R01 - Associate Scientist
Job Code: 600061
Management Level: J040
Reports to
Group Lead
Location(s)
Global Technology & Engineering (GTE), IITM-RP.
Job Summary ( Summarize the primary purpose & key accountabilities of the job function.)
Responsible for Analytical Method development, Method Validation, Method transfer, Routine analytical and stability study support for API, Intermediates and different DP formulations with the guidance and mentorship by senior chemist or superavisor.
Job Responsibilities ( Indicate the primary responsibilities critical to the job function.)

  • Responsible to Perform all activities as per GxP
  • He should adhere both quality and safety compliance according to organizational policies/procedures and regulatory guidelines.
  • Responsible for development analytical methods and analytical method validation by UPLC, HPLC, GC, for API, DP, Intermediate and Raw materials.
  • Support the analytical activities of lab trial batches, feasibility batches, lab scale batches, stability batches, stability studies as per plan.
  • Perform assessments of existing data packages, feasibilities and concluded remediation.
  • Ensure technical output is compliant with all Global Training Curriculum for the Instrument operations, material handling and Certifications related to Quality Operations, Manufacturing and EHS.
  • Ensures Compliances to local and corporate procedures and ensures all data packages are audit ready and transferable.


Coordinate with cross functional teams to ensure timely execution and resolution of all Deliverable versus target milestones
Qualifications/Skills: Education - Experience - Additional Requirements ( Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications, and other job-related technical and managerial skills.)
Requirements for all Global Job Levels
PREFERRED QUALIFICATIONS

  • M.Sc in Chemistry./M.Pharm


PREFERRED YEARS OF EXPERIENCE

  • 0 to 3 years of Experience


TYPE OF EXPERIENCE

  • Experience in Analytical Research and Development, possesses knowledge of oral solid dosage forms, liquids, semisolids, and API.
  • Theoretical knowledge on Chromatographic technic and spectroscopic technic.
  • Knowledge in basic technique like UV, IR, pH , Titration etc.,


Organizational Relationships: (Provide the primary groups or key role(s) that this role will interact with as a regular part of the job responsibilities. Include any external interactions as appropriate.)

  • Small Molecule Technology
  • Global Technology & Engineering
  • Launch Excellence
  • Pfizer Manufacturing Sites
  • External Supply
  • Global Supply Chain
  • Regulatory Sciences
  • Global EHS
  • Procurement
  • Pharmaceutical Sciences Small Molecule
  • Contract Research, Development and Manufacturing Organizations
  • Academic Institutes


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.
Research and Development
#LI-PFE

Top Skills

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What the Team is Saying

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The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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