Scientist

at  Viatris

Mylan Pharmaceuticals Inc.
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

• Access – Providing high quality trusted medicines regardless of geography or circumstance;
• Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
• Partnership – Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here’s how the role will make an impact:

Key responsibilities for this role include:

• Working in the Bioanalytical Laboratory at our world-class Research and Development Center, the incumbent will:
• Develop and validate analytical methods for the quantitation of small and large molecule drugs/metabolites (including peptides, proteins/antibodies, and oligonucleotides) and endogenous biomarkers in biological matrix using LC-MS/MS, and other techniques in support of both preclinical and clinical projects for PK, PD and biomarker assessments.
• Become fluent in operations of scientific equipment such as triple quadrupole and high-resolution mass spectrometers, chromatographic systems, and spectrometric/electrochemical plate readers.
• Review and approve data and evaluate the scientific validity of the conclusions derived.
• Author, review and/or approve technical documents such as analytical methods and reports.
• Maintain professional and technical knowledge by attending workshops and reviewing publications.
• Present scientific work within and across functions, and in professional symposia/conferences.
• Train and mentor junior associates in the organization.

The minimum qualifications for this role are:

• A degree in Chemistry, Biochemistry, Molecular/Cell Biology, immunology or a related discipline is required. A Bachelor’s degree and at least 7 years of experience, a Master’s degree and at least 2 years of experience, or a Doctorate and 0-2 years of experience is preferred. However, a combination of experience and education will be taken into consideration.
• Must possess knowledge of laboratory analytical theories, techniques and instrumentation employed in the quantitation/analysis of drugs and metabolites (e.g., HPLC, mass spectrometry, immunoassay, UV/Vis Fluorescence plate readers, automated sample processing equipment, etc.).
• Must have hands-on experience in utilizing LC-MS/MS instrument for drug and biological molecular analysis.
• Must be a team player, and possess excellent communication (oral and written), analytical and organizational skills.
• Must be able to multi-task and drive multiple projects and assigned responsibilities.
• Must possess the ability to write comprehensive technical reports and communicate complex concepts to colleagues across functions.
• A general understanding of current regulatory policies applicable to pharmaceutical industry practice and health authority regulations and expectations.
• Proficiency in speaking, comprehending, reading, and writing English is required.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

Key responsibilities for this role include:

• Working in the Bioanalytical Laboratory at our world-class Research and Development Center, the incumbent will:
• Develop and validate analytical methods for the quantitation of small and large molecule drugs/metabolites (including peptides, proteins/antibodies, and oligonucleotides) and endogenous biomarkers in biological matrix using LC-MS/MS, and other techniques in support of both preclinical and clinical projects for PK, PD and biomarker assessments.
• Become fluent in operations of scientific equipment such as triple quadrupole and high-resolution mass spectrometers, chromatographic systems, and spectrometric/electrochemical plate readers.
• Review and approve data and evaluate the scientific validity of the conclusions derived.
• Author, review and/or approve technical documents such as analytical methods and reports.
• Maintain professional and technical knowledge by attending workshops and reviewing publications.
• Present scientific work within and across functions, and in professional symposia/conferences.
• Train and mentor junior associates in the organization

The minimum qualifications for this role are:

• A degree in Chemistry, Biochemistry, Molecular/Cell Biology, immunology or a related discipline is required. A Bachelor’s degree and at least 7 years of experience, a Master’s degree and at least 2 years of experience, or a Doctorate and 0-2 years of experience is preferred. However, a combination of experience and education will be taken into consideration.
• Must possess knowledge of laboratory analytical theories, techniques and instrumentation employed in the quantitation/analysis of drugs and metabolites (e.g., HPLC, mass spectrometry, immunoassay, UV/Vis Fluorescence plate readers, automated sample processing equipment, etc.).
• Must have hands-on experience in utilizing LC-MS/MS instrument for drug and biological molecular analysis.
• Must be a team player, and possess excellent communication (oral and written), analytical and organizational skills.
• Must be able to multi-task and drive multiple projects and assigned responsibilities.
• Must possess the ability to write comprehensive technical reports and communicate complex concepts to colleagues across functions.
• A general understanding of current regulatory policies applicable to pharmaceutical industry practice and health authority regulations and expectations.
• Proficiency in speaking, comprehending, reading, and writing English is required