Opening At US For Research And Development Department At Cambrex

Company Information

You Matter to Cambrex.

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 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

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Opening At US For Research And Development Department At Cambrex

JobEngine
May 2, 2023
3 min read




Company Information

You Matter to Cambrex.

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 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

Your Work Matters.

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 medical, dental, vision, Life, LTD, retirement savings and more! Can we make this broader language, so it fits in all markets, e.g., that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

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!

Job Overview

With minimal supervision: perform analytical testing on reference standards and drug substance following established methods under GMP conditions. Maintain laboratory notebook and perform some data review. Maintain lab instruments with support. Ensure compliance with applicable company SOPs and regulatory guidance.

With some supervision: conduct method validation and method transfers; support laboratory investigations, author reports.

Responsibilities

Perform analytical testing utilizing established methods.
Maintain and review notebook and data entries.
Write reports and similar documents
Conduct reference standard characterizations
Conduct analytical methods validation, and transfers
Maintain equipment.
Responsible for laboratory upkeep (supplies, chemicals, cleanliness, safety).
This position works with and handles hazardous materials and wastes. Responsible for recognizing emergency situations concerning hazardous materials and wastes.
Write protocols and analytical procedures.

Education, Experience & Licensing Requirements

Minimum BS/BA in Chemistry or related field with 6 years experience in a laboratory environment or MS in Chemistry or related field with 2 years experience.

Fundamental Understanding with some of the following analytical technologies:
Titrations (manual and automated)
Basic wet chemistry
FTIR, NMR, XRPD, HPLC, GC

Working knowledge of other analytical equipment common to the pharmaceutical industry

Competencies:

Analytical Chemistry Knowledge: Some understanding of the principles of Analytical Chemistry, able to execute protocols

Cross Discipline Knowledge: Early practical industry exposure to cross functional technical departments, including organic chemistry, works with QC/PSG for transfer

GMP/Regulatory Knowledge: With less manager supervision, able to better understand need for SOPs and basic regulatory guidance, knowledgeable of AD requirements


Instrumentation: Basic understanding of key analytical R&D equipment, can operate independently once instructed, solid LC/GC

Communication: Good oral and written communication skills within group

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, review notebooks and spreadsheets

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