Associate Scientist II, Analytical Process & Development (ARD)

Veranova, L.P; Massachusetts; On-site; USD 65,000 - 80,000; Full time

Benefits offered by this job

Comprehensive health & wellness benefits

Generous PTO and holiday pay

Competitive base salary with performance-based bonuses

401(k) plan with company match

Tuition assistance for degree programs

Job summary

A leading pharmaceutical company is seeking an Associate Scientist II to develop and implement analytical procedures for active pharmaceutical ingredients. This role involves performing sample analysis, assisting with method development, and ensuring compliance with cGMP standards. Qualified candidates should have a BS in Analytical Chemistry or equivalent experience. The position offers a salary range of $65,000-$80,000 annually and includes comprehensive health benefits, professional development opportunities, and a commitment to an inclusive culture.

Qualifications

• Experience in analytical development (R&D and method qualification/validation) in pharma.
• Ability to work independently and in a team environment.
• Familiarity with cGMP environment.

Responsibilities

• Perform sample analysis and document results according to SOPs.
• Assist with method development and validation.
• Prepare high-quality written documentation.
• Communicate research results effectively.
• Demonstrate initiative and collaborate with team members.
• Apply cGMP and compliance standards.

Skills

Proficiency in HPLC

Proficiency in GC

Proficiency in FTIR

Good written and verbal communication skills

Knowledge of MS Project

Education

BS in Analytical Chemistry or equivalent with 2+ years experience

MS in Analytical Chemistry or equivalent with 1+ years experience

Job description

Associate Scientist II, Analytical Process & Development (ARD)

3 days ago Requisition ID: 1548

Role Overview

The Associate Scientist II, ARD is responsible for development and implementation of analytical procedures and specifications in support of the development and manufacture of active pharmaceutical ingredients (APIs) for traditional synthetic molecules (including potent) and peptides. Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (NMR, ICP-MS, FTIR and UV-Vis), and physical properties (particle size, water content, etc.). The Associate Scientist II is expected to support the functions including sample analysis by a variety of analytical techniques with respect to potent compounds. This role is 100% on site at our Devens, MA facility.

Core Responsibilities

• Performs sample analysis, interprets results, and reports data. Documents all analyses per SOPs.
• Assists with method development, method qualification/validation/transfer activities, drafts weekly reports, method qualification/validation protocols/reports for analytical procedures.
• Prepares high quality written documentation (notebook entry, summary reports, SOPs, analytical procedures, etc.). Troubleshoots analytical instrumentation.
• Communicates effectively in verbal and written form on research results and plans.
• Demonstrates initiative in handling responsibilities and collaborates with team members. Participates in self‑development activities.
• Applies cGMP, quality, regulatory, and EH&S standards in compliance with company procedures and state and federal regulations.
• Promotes a safe and compliant work environment by following EH&S policies, reporting incidents, and supporting corrective actions and sustainability initiatives.

Qualifications

• BS in Analytical chemistry or equivalent with 2+ years relevant experience or MS in Analytical chemistry or equivalent with 1+ years of related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry in a cGMP environment.
• Proficiency in standard analytical techniques such as: HPLC, GC, UV, KF, and FTIR.
• Good written and verbal communication skills. Ability to work independently and in a team environment.
• Knowledge of MS Project. Experience in establishing integrated plans with resource and task constraints.

Salary Range

$65,000-$80,000 annual base salary.

The salary range for this role is $65,000-$80,000. This range represents a good‑faith estimate of the compensation we expect to offer for this position at the time of posting. Actual compensation will be based on factors such as relevant experience, skills, qualifications, and internal equity. In exceptional cases, compensation may exceed the stated range.

Our Commitment

• Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
• Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance‑based bonuses, and an attractive 401(k) plan with company match.
• Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition assistance for undergraduate and graduate degree programs.
• Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.

Additional Information

Applicants for this role must be authorized to work in the United States without further employer sponsorship.

Equal Opportunity Employer

Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.

All your information will be kept confidential according to EEO guidelines.