Veranova→
Associate Scientist II, Analytical Process & Development (ARD)
Entry LevelOn-site
Location
Devens, MA
Salary
$65k–$80k/yr
Experience
Not specified
Posted
3 weeks ago
Skills
analytical chemistryanalytical developmentmethod qualificationmethod validationchromatographyhplcuplcgas chromatographygcion chromatographyicspectroscopynmricp-msftiruv-viskarl fischer titrationcgmpms project
Job Description
Summary: Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. The Associate Scientist II, ARD is responsible for the development and implementation of analytical procedures and specifications in support of the development and manufacture of APIs, utilizing various analytical techniques.
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 collaborative 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
Required 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
Required Skills: Analytical Chemistry, Analytical Development, Method Qualification, Method Validation, Chromatography, HPLC, UPLC, Gas Chromatography, GC, Ion Chromatography, IC, Spectroscopy, NMR, ICP-MS, FTIR, UV-Vis, Karl Fischer Titration, cGMP, MS Project
Benefits: Comprehensive health & wellness benefits., Access to mental health resources and wellness programs., Generous PTO and holiday pay policies., Eligibility for performance-based bonuses., Attractive 401(k) Plan with company match., Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship., Tuition Assistance for Undergraduate and Graduate degree programs.
Benefits
Comprehensive health & wellness benefits.
Access to mental health resources and wellness programs.
Generous PTO and holiday pay policies.
Eligibility for performance-based bonuses.
Attractive 401(k) Plan with company match.
Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship.
Tuition Assistance for Undergraduate and Graduate degree programs.