Scientist 2 - QC (2nd Shift 3-11pm)

Cambrex•High Point, NC

12h•Onsite

About The Position

The Scientist 1 - Quality Control role performs routine analytical testing on raw materials, intermediate, and final products as well as in-process testing; performs data entry; draft deviations, and participates in OOS investigations for their testing. Ensures compliance with applicable Company SOPs and regulatory guidance’s. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We’re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more! Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Requirements

Analytical Chemistry Knowledge: Some understanding of the principles of Analytical Chemistry or Quality Control
Cross Discipline Knowledge: Early practical industry exposure to cross functional technical departments, including organic chemistry
GMP/Regulatory Knowledge: With less manager supervision, able to better understand need for SOPs and basic regulatory guidance
Instrumentation: Basic understanding of key analytical R&D equipment, can operate independently once instructed
Communication: Good oral and written communication skills
Problem Solving: May be asked to support peer-led laboratory investigation process with manager support
Time Management: Ability to handle key assignments, with supervision
Leadership: Shares ideas with peers
Technical Documentation and Review: Ability to keep a good laboratory notebook and perform data entry, compliance with GDP
External Influence: Ability to work within a matrix team
Industry Credibility and Rapport: Willing to learn and grow within the local Cambrex Team
Operational Excellence: Strives to engage in group/team improvement projects
Change Orientation: Able to understand the importance of Cambrex initiatives
Experience with and fundamental understanding of several of the following analytical technologies ( - most important): HPLC FTIR Titration Basic wet chemistry NMR XRPD cKF
Working knowledge of other analytical equipment common to the pharmaceutical industry
This position works with and handles hazardous materials and wastes at Cambrex. This person has the appropriate qualifications to read, understand, apply and communicate written and verbal information regarding handling and managing hazardous wastes. He/She is also responsible for recognizing emergency situations concerning hazardous materials and wastes.

Responsibilities

Perform routine testing of raw materials, intermediate, and final products (may include stability)
Provide support to the plant by performing in-process testing and analyzing cleaning samples.
Maintain laboratory notebook.
Ensure equipment is left in good working order after use.
Perform laboratory upkeep (wash glassware, reorder supplies, check for expired chemicals).
Draft their deviations.
Be an active participant in their laboratory investigations.