Associate Scientist II, Analytical Research & Development (ARD)

Veranova; Harvard (MA); On-site; USD 65,000 - 80,000; Full time

Benefits offered by this job

Comprehensive health & wellness benefits

401(k) Plan with company match

Tuition Assistance

Generous PTO

Job summary

A global leader in pharmaceutical manufacturing is seeking an Associate Scientist II in Analytical Process & Development. The role focuses on analytical procedure implementation in the manufacturing of APIs. Candidates should have a BS or MS in Analytical Chemistry, relevant experience in a cGMP environment, and proficiency in HPLC, GC, and FTIR. The position offers a salary range of $65,000-$80,000, comprehensive health benefits, and opportunities for professional development.

Qualifications

• 2+ years relevant experience in a cGMP environment or 1+ year with MS.
• Proficiency in standard analytical techniques such as HPLC, GC, UV, and FTIR.
• Good written and verbal communication skills.

Responsibilities

• Performs sample analysis and interprets results.
• Assists with method development and documentation.
• Communicates results effectively in verbal and written form.

Skills

HPLC

GC

UV

FTIR

Analytical chemistry knowledge

Education

BS in Analytical chemistry

MS in Analytical chemistry

Tools

MS Project

Job description

Associate Scientist II, Analytical Process & Development (ARD)

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Every role at Veranova plays a part in delivering an exceptional customer experience through ownership and integrity.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

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 the 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.

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. Even if you don’t meet every qualification, we encourage you to apply. 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.

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

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 applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.