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Operations Technician

Job in Waterford, New London County, Connecticut, 06386, USA
Listing for: Cambrex
Full Time position
Listed on 2026-01-22
Job specializations:
  • Manufacturing / Production
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Cambrex Operations Technician

IE--Waterford

Job :

Type: Regular Full-Time

Category: Stability Storage

Location: Cambrex - Waterford

Overview

Through our support of international pharmaceutical and medical device companies, we see Q1 Scientific as part of a customer’s operational and production chain. The healthcare products provided by these companies are vital and we are privileged to perform our part in the provision of those products to the global market.

Our purpose-built facilities in Waterford and Belgium offer walk-in rooms and reach-in cabinets for sample storage at specific temperature and humidity conditions ranging from ultra-low freezers at
-80°C to storage over 50°C. This Operations Technician position in Waterford offers the opportunity to build your experience across operations and quality. Working as part of a busy Operations team, you will report to the Stability Lead while performing sample management activities.

Responsibilities

Operations

  • Receive and check customer deliveries to Q1 Scientific, highlighting any anomalies and ensuring secure, correct and timely storage of such deliveries in line with customer requirements, regulatory and quality guidelines
  • Take responsibility for retrieval, packing and delivery of samples back to customers
  • Perform daily checks on stability cabinets/room conditions
  • Ensure the facility is kept clean and equipment and maintenance schedules are maintained as specified by the Quality Management System (QMS)
  • Liaise with external consultants and contractors
  • Provide general admin support and any other duties as may be required

Quality

  • Ensure that all activities meet the quality standards specified by the Q1 Scientific QMS and in accordance with cGMP standards
  • Review completed documents for compliance to specification and to ensure all entries are complete
  • Produce and manage quality reports around deviations
Qualifications / Skills
  • Strong attention to detail, ability to work on own initiative, and highly motivated
  • Ability to work to strict deadlines, be a team player with well-developed problem-solving abilities
  • Highly numerate, computer literate with Microsoft Word and Excel skills to produce graphs and reports
  • A good work ethic, highly flexible and willing to work as part of a team or on your own initiative
  • A positive attitude to work and a willingness to take ownership of projects, client relationships and timely responses and reporting
Qualifications

The ideal candidate will have 2 + years’ work experience in a temperature-controlled storage environment (retail or warehouse), regulated manufacturing or pharmacy environment with:

  • Experience working to standard operating procedures in a regulated environment (this is desirable and not essential)
  • Previous experience in picking and packing materials
  • Experience using an inventory management system
  • The ability to complete quality documentation/reports

This is a full-time, permanent position. Hours are 8.30 am to 5 pm Monday – Friday, with some requirement to work outside of these hours.

Equal employment opportunity, including veterans and individuals with disabilities.

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