Pfizer
Scientist=Chem Analytical
Pfizer, Jackson, Mississippi, United States
Scientist - Chem Analytical
Location: AT-GTEL, Chennai Role Title:
Scientist (Chem Analytical) Global Job Levels: Job Family Group:
Research and Development Job Family:
093- Chemistry-Analytical Job Category:
Research Job Level:
R03 - Scientist Job Code:
602741 Management Level:
J060 (06C) Why Patients Need You: Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Accountability: Responsible for E&L workflow support for a variety of pharmaceutical matrices, including aqueous buffered saline solutions, complex pharmaceutical formulations, and very complex matrices. This includes activities such as Analytical Method development, Method Validation, Investigation, Tox assessment, and Regulatory support. What You Will Achieve: As a Scientist, you will be at the center of our operations, performing qualitative and quantitative analyses of organic, inorganic compounds, or biologics. You will use your scientific judgment to adapt standard methods and techniques and undertake mentoring activities to guide your team members. Responsibilities: Should have extractables and leachable testing experience for pharmaceutical and biopharmaceutical products as: Primary packaging for pharmaceuticals (inhalation, parenteral, ophthalmic, topical, and oral drug forms). Secondary packaging. Delivery systems. Single-use systems or other process materials used during pharmaceutical manufacturing. Leachable Method Development and Validation. Leachable Studies on Stability Samples. Test According to International Standards: Physico-chemical testing according to compendium monograph. Extractables & Leachables assessments for finished packaging. Sound scientific research leachables-screening studies. Leachables shelf-life studies. Quantitative and qualitative determinations of plastic additives and related substances. Should be conversant with the below analytical Techniques: Headspace coupled to gas chromatography with mass spectral detection (HS-GC/MS). Gas chromatography with mass spectral detection (GC/MS). Liquid chromatography with mass spectral detection (LC/MS/MS). Inductively coupled plasma with optical emission detection (ICP-OES) and ICP-MS. Infrared spectrophotometry (FTIR). Wet chemical methods: pH, TOC, conductivity, and others. Toxicological assessments of extractables/leachables studies for medicinal products: Derivation of health-based thresholds. In silico toxicology for the assessment of substances. Other experiences: Ensure technical output is compliant with all Global Training Curricula. Work with Quality Assurance and cross-functional teams. Ensure compliance to local and corporate procedures. Coordinate with cross-functional teams. Requirements for all Global Job Levels: Preferred Qualifications: MSc / Mpharm / Ph.D Preferred years of experience:
9 to 12 years of Experience. Experience in interdisciplinary drug development teams and industrial experience developing analytical strategies. Relationships: Small Molecule Technology Global Technology & Engineering Launch Excellence Pfizer Manufacturing Sites External Supply Global Supply Chain Regulatory Sciences Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.
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Location: AT-GTEL, Chennai Role Title:
Scientist (Chem Analytical) Global Job Levels: Job Family Group:
Research and Development Job Family:
093- Chemistry-Analytical Job Category:
Research Job Level:
R03 - Scientist Job Code:
602741 Management Level:
J060 (06C) Why Patients Need You: Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Accountability: Responsible for E&L workflow support for a variety of pharmaceutical matrices, including aqueous buffered saline solutions, complex pharmaceutical formulations, and very complex matrices. This includes activities such as Analytical Method development, Method Validation, Investigation, Tox assessment, and Regulatory support. What You Will Achieve: As a Scientist, you will be at the center of our operations, performing qualitative and quantitative analyses of organic, inorganic compounds, or biologics. You will use your scientific judgment to adapt standard methods and techniques and undertake mentoring activities to guide your team members. Responsibilities: Should have extractables and leachable testing experience for pharmaceutical and biopharmaceutical products as: Primary packaging for pharmaceuticals (inhalation, parenteral, ophthalmic, topical, and oral drug forms). Secondary packaging. Delivery systems. Single-use systems or other process materials used during pharmaceutical manufacturing. Leachable Method Development and Validation. Leachable Studies on Stability Samples. Test According to International Standards: Physico-chemical testing according to compendium monograph. Extractables & Leachables assessments for finished packaging. Sound scientific research leachables-screening studies. Leachables shelf-life studies. Quantitative and qualitative determinations of plastic additives and related substances. Should be conversant with the below analytical Techniques: Headspace coupled to gas chromatography with mass spectral detection (HS-GC/MS). Gas chromatography with mass spectral detection (GC/MS). Liquid chromatography with mass spectral detection (LC/MS/MS). Inductively coupled plasma with optical emission detection (ICP-OES) and ICP-MS. Infrared spectrophotometry (FTIR). Wet chemical methods: pH, TOC, conductivity, and others. Toxicological assessments of extractables/leachables studies for medicinal products: Derivation of health-based thresholds. In silico toxicology for the assessment of substances. Other experiences: Ensure technical output is compliant with all Global Training Curricula. Work with Quality Assurance and cross-functional teams. Ensure compliance to local and corporate procedures. Coordinate with cross-functional teams. Requirements for all Global Job Levels: Preferred Qualifications: MSc / Mpharm / Ph.D Preferred years of experience:
9 to 12 years of Experience. Experience in interdisciplinary drug development teams and industrial experience developing analytical strategies. Relationships: Small Molecule Technology Global Technology & Engineering Launch Excellence Pfizer Manufacturing Sites External Supply Global Supply Chain Regulatory Sciences Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.
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