Quality Technician, Waterford

Job Description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

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 environmentstrengthen 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!

Your Future Matters.

Job Overview

We are seeking applicants for the position of Quality Technician to join our team. This role will report directly to the Quality Manager for Waterford and will be a pivotal role in our growing Quality department.

Responsibilities

Quality Management System (QMS)

Provision of assistance and advice to the Company on all QMS activities.Ensure that all Q1 activities meet the quality standards specified by the Company QMS and in accordance with cGMP standards.Continually monitors the QMS system suggesting improvements and CAPA measures.Ensure all planned and unplanned changes (deviations) are adequately investigated and documented.Review of completed documents for compliance to specification and to ensure all entries are complete.Proposing/reviewing document changes as appropriateMaintenance of indexes (electronic and hard copy)Issue of document numbers and controlled documents (logbooks, protocols for execution etc.)Providing admin assistance to the Company on all eQMS activitiesWorking in collaboration with team members

Audits:

Ensure compliance to GMP certification by conducting and reporting internal reviews.Co-ordinates and prepares for all internal, regulatory, supplier and customer audits.
Qualifications/Skills

Strong attention to detail and organisational skills
Education, Experience & Licensing Requirements

A degree in a science-related discipline (desirable)Experience working in a regulated environment (advantageous)1–2 years’ experience in a quality or administrative role (preferred)Strong attention to detail and organisational skills

Hours of Work

This is a full time, permanent position

Hours are to 5pm, Monday – Friday

Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre-employment screen. The pre-employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration. 

All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law.