Quality Control Analyst

Veranova L PDevens, MA
5d

About The Position

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse 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. 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. The QC Analyst I will perform laboratory analysis and sampling of raw materials, intermediates, finished products, cleaning verification samples, stability samples and other miscellaneous samples following relevant SOP’s while adhering to current Good Manufacturing Practices (cGMP) to ensure they meet the required quality standards and specifications. This role also involves basic maintenance of technical equipment, use of basic troubleshooting techniques and laboratory stock management.

Requirements

  • BS in Chemistry, or equivalent
  • Ability to work independently with minimal supervision and in a team environment
  • Ability to read, analyze, and interpret English-language chemical periodicals, scientific journals, and regulatory documents

Nice To Haves

  • Experience with common analytical techniques such as HPLC/UPLC, GC, NMR, UV-Vis, pH meter, KF, FTIR, PSD or Refractive index is preferred
  • Previous experience with Laboratory Information Management Systems (LIMS)

Responsibilities

  • Deliver experimental output with a high degree of scientific integrity, both on time and on target, with a focus on quality
  • Actively demonstrate strict compliance with current Good Manufacturing Practices and Good Documentation Practices (cGMP and GDP), Environment, Health and Safety (EH&S) and other relevant standards in all aspects of work
  • Manages data by following established procedures, standards and processes. Uses the concepts of ALCOA+ to maintain Data Integrity
  • Perform maintenance and calibration of technical equipment with ability to perform simple troubleshooting
  • Creates, maintains, analyses and/or updates QC data with minimal supervision following established methods and relevant specifications
  • Always ensures the security and safe handling of all controlled substances. Strictly adheres to all Company and DEA regulations. Ensures that waste is appropriately characterized, labelled, stored and disposed in compliance with all Company, state and federal regulations
  • Other responsibilities as assigned

Benefits

  • Health & Wellness: Comprehensive health & Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
  • Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and 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 are committed to ensuring that everyone can bring their full self to work and thrive in their career.
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