Qualifications:

Education and Experience:

Degree in chemistry, biochemistry, molecular biology, or related scientific disciplines that combine chemistry and biology, plus pharmaceutical industry, regulated industry, or Information Science experience - Bachelor's and 5+ years, Master's/PhD and 3+ years

Required:

Completed at least one year of organic chemistry Experience or familiarity with deriving chemical nomenclature (IUPAC or CAS style) Experience with structure drawing software (ChemDraw, ACD, Accerlys, etc.) Domain expertise: Strong knowledge of chemical structures, stereochemistry, physicochemical properties, biological sequence representations and concepts, and the drug development process Familiarity with chemical identifiers and formats (SMILES, InChI, CAS, MOL/SDF), spectral data concepts, chemical ontologies/taxonomies, and common cheminformatics tools or libraries Experience establishing stewardship frameworks, SOPs, ownership models, and KPIs to maintain high quality, traceable, and compliant data Demonstrated history of adopting new technologies (AI, ML-assisted curation, knowledge graphs) and willingness to learn & prototype new approaches Very organized and able to work with high attention to detail Excellent written and verbal communication skills with the ability to convey technical and business information Ability to present in a group environment Strong time management and project management skills Ability to balance and prioritize multiple tasks Ability to work under pressure in a changing environment with flexibility Ability to work independently to drive tasks to completion and to act with appropriate accountability Ability to establish and maintain good working relationships with the different functional areas and work cross functionally as part of a team Preferred qualifications: Experience with searching resources (SciFinder, STN) and familiarity with structure searching. Data modeling & metadata: Ability to understand canonical data models for products, substances and related metadata, with understanding of identifiers, keys, versioning, and provenance. Familiarity with data standards and ontologies used in the biomedical/pharma domain (WHO Drug, Med

DRA, CDISC, MESH, UMLS

). Experience with database querying (SQL), and data visualization tools Proficiency with programming languages, such as python or R Skilled at defining validation rules, implementing automated checks, resolving duplicates/merges, and maintaining robust audit trails. Knowledge of how GxP, GLP, 21 CFR part 11, REACH, and IDMP standards influence data management practices #eligiblefor

ERP BARDS2020

Required Skills:

Adaptability, Biopharmaceutical Industry, ChemDraw, Data Integrity, Data Management, Data Modeling, Data Standards, Data Systems, Good Manufacturing Practices (GMP), Ontology, Pharmaceutical Industry, Regulated Industries, Standard Operating Procedure (SOP)

Preferred Skills:

Current Employees apply HERE Current Contingent Workers apply

HERE US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights

EEOC GINA

Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:

We will consider qualified applicants with arrest and conviction records for employment in compliance with the

San Francisco Fair Chance Ordinance Los Angeles Residents Only:

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular Relocation:

No relocation

VISA Sponsorship:

No Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid Shift:

Not Indicated Valid Driving License:

No Hazardous Material(s):

N/A Job Posting End Date:

08/3/2026 •A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. 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