FreshRemote.Work

Scientist, Analytical Research and Development

USA - New Jersey - Rahway, United States

Job Description

The Small Molecule Analytical Research and Development group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

In your role as Scientist, you will be part of a team of Analytical Chemists working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis. 

Primary Responsibilities

  • Support execution of Good Manufacturing Practices (GMP) activities such as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools.

  • Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA principles.

  • Troubleshoot and investigate any challenges associated with the GMP testing through active collaboration with cross-functional project teams and/or Quality stakeholders.

  • Validate and implement analytical methods to support release and stability testing of clinical materials.

  • Perform data entry, data review, and author analytical reports or data summaries.

  • Strong collaboration with fellow Analytical Research & Development colleagues as well as cross-functional partners such as Global Development Quality, Process Chemistry, and Pharmaceutical Operations.

  • Support compliance audit/inspection activities.

Education Minimum Requirements:

  • Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree or Master of Science degree in Chemistry, Pharmaceutical Sciences, or other Life Sciences.

Required Experience and Skills

  • Excellent written and oral communication skills, as well as interpersonal skills, are necessary to qualify for this role.

  • Candidates will also be required to work in a team environment with cross-functional interactions.

Preferred Experience and Skills

  • Though not required, the ideal applicant would have hands-on experience in GMP operations, advanced chromatographic separation science, spectroscopy analysis, dissolution testing, and other analytical techniques. 

  • In addition, experience with Empower, data science, and LCMS are also a plus.

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.

We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace.  All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

Pay Transparency Nondiscrimination

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas 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

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

Expected US salary range:

$85,600.00 - $134,800.00

Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.

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:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

Yes

Job Posting End Date:

02/26/2025

*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.

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Job Profile

Regions

North America

Countries

United States

Restrictions

Hybrid Hybrid work Hybrid work model On-site Puerto Rico residents only Travel required US and Puerto Rico residents only

Benefits/Perks

Bonus eligibility Career development opportunities Collaboration Collaboration with talented colleagues Diverse workplace Equal opportunity Equal opportunity employer Flexible work Flexible work arrangements Global team Hands-on experience Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Inclusive workplace Insurance Paid holidays Retirement benefits Sick Days Team environment Vacation

Tasks
  • Author analytical reports
  • Collaboration
  • Communication
  • Compliance
  • Data Analysis
  • Document experiments
  • Execution
  • Innovation
  • Perform data entry
  • Support GMP activities
  • Troubleshoot GMP testing
  • Validate analytical methods
Skills

Analysis Analytical Analytical Chemistry Analytical Methods Analytical Research Analytical Techniques Analytical tools APIs Audit Characterization Chemistry Chromatographic separation Clinical Collaboration Communication Compliance Data Data analysis Data Entry Data Review Data Science Development Dissolution testing Drug delivery Drug Development Education Empower Execution GMP Good Manufacturing Practices Inclusion Innovation Interpersonal Laboratory LCMS Life sciences Manufacturing Manufacturing Practices Manufacturing processes Operations Oral communication Organization Peptide Pharmaceutical Pharmaceutical operations Pharmaceutical Sciences Process Chemistry Quality Research Research and development Science Spectroscopy Statistical Data Analysis Teams Testing

Experience

3 years

Education

AS Bachelor Bachelor of Science Business Chemistry Data Science Degree Development Health Care Life Sciences Master Master of Science Pharmaceutical Sciences Science

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9