Senior Manager, Analytical Chemistry

Rhythm Pharmaceuticals Inc.

Boston (MA)

Hybrid

USD 135,000 - 215,000

Full time

2 days ago
Be an early applicant

Get more replies from employers

Send a job-specific resume in minutes.

Benefits offered by this job

Hybrid work model
Competitive compensation

Job summary

Rhythm Pharmaceuticals Inc. in Boston, MA is seeking an Analytical Chemistry Manager to oversee testing at contract sites and guide CMOs on analytical methods. You will lead method development, validation, transfer, and regulatory documentation for in‑process yield, purity, and impurities. Travel may be required, and a hybrid work model is offered.

Qualifications

  • Bachelor’s degree with 7+ years or Master’s degree with 5+ years in analytical method development or QC in pharma.
  • Experience in analytical techniques for monitoring yield and purity during organic synthesis.
  • Knowledge of testing of raw materials, excipients and components.
  • Familiarity with characterization, qualification and management of impurity standards.
  • Authorship/review of analytical method development, validation, and transfer docs.
  • Knowledge of ICH, compendium, cGMP and pharma best practices.
  • Experience with trace impurities qualification (extractables/leachables/nitrosamines).
  • Proficient in LC methods, MS, GC, moisture analyses, and related analytical procedures.
  • Proficient with LC chromatographic analyses, statistics, and quality systems.
  • Excellent interpersonal, organizational, and communication skills.

Responsibilities

  • Direct development, optimization, validation, and transfer of analytical procedures for in-process yield and impurities.
  • Coordinate analytical activities at CMOs/CROs with cross-functional teams.
  • Assist in deviations remediation, investigations, CAPAs, and change controls.
  • Author/review CMC submissions for analytical sections and stability data.
  • Manage analytical documents for lifecycle management of methods and specs.
  • Select CRO/CMOs, solicit quotes, and finalize contracts with finance/legal.
  • Support pre- and post-approval commitments and annual product reviews.

Skills

HPLC
GC
MS
Moisture analyses
LC chromatographic analyses

Education

Bachelor’s degree in analytical chemistry or related field
Master’s degree in analytical chemistry or related field

Tools

Statistical software
Quality management systems

Job description

Company Overview

Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.

Company Overview

Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.

Opportunity Overview

The Analytical Chemistry Manager is responsible for oversight of testing performed at Rhythm’s contract sites to support manufacturing. The qualified candidate will provide directions to CMO analytical laboratories and serve as subject matter expert on cross functional project teams (internal and external). The ideal candidate will be knowledgeable in analytical techniques used for testing excipients, raw materials, components, in-process reactions and purifications.

Responsibilities And Duties
  • Direct the development, optimization, validation, and transfer of analytical procedures for testing and control of in-process yield, purity, key intermediates and impurities.
  • Participate in cross-functional task forces to coordinate analytical activities at CMOs/CROs.
  • Contribute to remediation of deviations and investigations, implementation of corrective / preventive actions and change controls.
  • Author and review regulatory CMC submissions including analytical procedures, method validations, reference standards, batch analyses, characterization, stability, and specification sections.
  • Identify, review, and organize analytical documents to support robust analytical method life-cycle management.
  • Assess and select CRO/CMOs, solicit quotes and finalize contracts with finance and legal.
  • Contribute to fulfilment of pre- and post-approval commitments and annual product reviews.
Qualifications And Skills
  • Minimum of Bachelor’s degree with over 7 years’ experience or Master’s degree with over 5 years’ experience in analytical method development or quality control in the pharmaceutical industry.
  • Experience in analytical techniques for monitoring yield and purity during organic synthesis.
  • Knowledgeable in the testing of raw materials, excipients and components.
  • Familiarity in procedures for characterization, qualification and management of intermediate and impurity standards.
  • Authorship and/or review of analytical method development, validation and transfer documents.
  • Demonstrated knowledge and experience in the interpretation and application of ICH, compendial, cGMP and pharmaceutical best practices.
  • Familiarity in qualification of trace impurities, including extractables, leachables and nitrosamines.
  • Well versed in analytical and characterization procedures, for example, HPLC, GC, MS, elemental impurities and moisture analyses.
  • Competent in the use of software applications, including LC chromatographic analyses, statistical applications, and quality management systems.
  • Excellent interpersonal, organizational, problem-solving, customer service and communication skills.
  • Self-motivated, flexible, and able to prioritize work and handle multiple assignments in a fast-paced environment, while maintaining a high level of scientific quality and compliance.

This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs.

This role may involve some travel.

The expected salary range for this position is $135,000 - $215,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job‑related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units.

More About Rhythm

We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.

At Rhythm our core values are:
  • We are committed to advancing scientific understanding to improve patients’ lives
  • We are inspired to tackle tough challenges and have the courage to ask bold questions
  • We are eager to learn and adapt
  • We believe collaboration and ownership are foundational for our success
  • We value the unique contribution each individual brings to furthering our mission

Inherent in our core values is the commitment to act ethically and with integrity in all we do.

Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law.

Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Senior Manager, Analytical Chemistry
Senior Manager, Analytical Chemistry

Rhythm Pharmaceuticals, Inc • Boston (MA), Northern (KY)

Hybrid
USD 135,000 - 215,000
Senior Director, Analytical Development & Quality Control
Senior Director, Analytical Development & Quality Control

Rhythm Pharmaceuticals Inc. • Boston (MA)

Hybrid
USD 210,000 - 300,000
Discretionary annual bonus
Restricted stock units
Benefits package
Senior Director, Analytical Development & Quality Control
Senior Director, Analytical Development & Quality Control

Rhythm Pharmaceuticals, Inc • Boston (MA)

Hybrid
USD 210,000 - 300,000
Director, Regulatory CMC
Director, Regulatory CMC

Rhythm Pharmaceuticals, Inc • Boston (MA)

Hybrid
USD 182,000 - 275,000
Discretionary bonus
Benefits package
Restricted stock units (RSUs)
+1
Associate Director, GCP/GLP/GVP QA
Associate Director, GCP/GLP/GVP QA

Rhythm Pharmaceuticals Inc. • Boston (MA)

Hybrid
USD 160,000 - 240,000
Discretionary annual bonus
Restricted stock units
Hybrid work model
Director, Regulatory CMC
Director, Regulatory CMC

Rhythm Pharmaceuticals Inc. • Boston (MA)

Hybrid
USD 182,000 - 275,000
Discretionary annual bonus
Restricted stock units
Director, Program Management
Director, Program Management

Rhythm Pharmaceuticals, Inc • Boston (MA)

Hybrid
USD 182,000 - 275,000
Hybrid work model
Annual bonus
RSUs
+1
Senior Manager, Business Analytics and Reporting
Senior Manager, Business Analytics and Reporting

Rhythm Pharmaceuticals Inc. • Boston (MA)

Hybrid
USD 135,000 - 215,000
Hybrid work model
Bonus potential
RSUs
Director, Nonclinical Development
Director, Nonclinical Development

Rhythm Pharmaceuticals Inc. • Boston (MA)

Hybrid
USD 182,000 - 275,000
Discretionary annual bonus
Restricted stock units
Comprehensive benefits
Associate Director, Biostatistics
Associate Director, Biostatistics

Rhythm Pharmaceuticals Inc. • Boston (MA)

Hybrid
USD 144,000 - 240,000
Hybrid work model
Discretionary annual bonus
Restricted stock units (RSUs)