- Develop safe, robust, scalable, and efficient manufacturing processes for intermediate and Active Pharmaceutical Ingredients (APIs) suitable for both pilot plant and commercial scale production.
- Performing literature search and identifying various synthetic routes for process development.
- Promotes the use of novel experimental approaches within sub-function; routinely investigates/creates innovative processes, hypotheses and methodologies.
- Knowledge of interpretation of structures using spectral techniques like NMR, IR & Mass spectra.
- Planning and Performing experiments as per process governance (Lab feasibility, Optimization, Pre-validation, CPP and Validation)
- Performing What if studies, stress studies, holding time studies, Mass balance, recovery studies and scale up studies.
- Encountering the process challenges on time and supporting production teams for scale up activities.
- Handling of business critical / supply chain critical related investigational projects on fast track
- Participate in brainstorming activity for the project in identifying scope of improvement
- Responsible for making necessary scientific statutory documents for the lab execution of a given project
- Designing experiments based on the project /business requirement in varying scale as per the needs
- Perform data analysis, interpret the data of them and provide scientific rationale for the experiments
- Support the next level manager in providing the cost estimates associated with R&D project proposals
- Summarize the experimental results and present to the next level managers for discussion
- Prepare Technical project updates with precious data as per the business meeting requirement regularly
- Knowledge on ICH guidelines.
- Willingness to learn and apply new technology/ tools to meet process / business needs
- Co-ordinate with Analytical, Process safety, Process engineering teams on the project discussions and support the need of them to drive the project
- Utilization of electronics tools (Biovia eLN, GDMS, LIMS etc.,)
- Partner closely with other CRD scientists, Process Engineers, Process Safety Chemists, Crystallization Technologists, Pilot Plant facility, Analytical, Formulation and manufacturing colleagues at Global Pfizer sites as required.
- Responsible for instrument qualification across the CRD labs (coordination with instrumentation team, quality team)
- Ensure compliance with cGMP /GSP procedures and practices
- Ensure effective safety systems are implemented in the premises
- Perform other tasks as per the dynamic business requirement
QUALIFICATION
- Ph.D in the field of Organic Chemistry.
- Demonstrated capabilities and experience in performing chemical reactions, structure characterizations, basic understanding of chromatography, Crystallizations, Basic safety principles, Basic quality principles, basic understanding of analytical techniques.
- Experience and demonstrated competencies in working with teams in a matrixed organization, building and nurturing relationships and effective engagement resulting in successful outcomes.
- Candidate should have skill in preparing the technical reports and adherence to compliance.
Work Location Assignment: On Premise
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
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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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