Chemist II (12 hours shift)

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Job Description

DESCRIPTION:

Join our Quality Control team at Thermo Fisher Scientific where you'll make meaningful contributions to our mission of enabling customers to make the world healthier, cleaner and safer. As an Engineer/Scientist II, QC, you'll perform testing and analysis to ensure product quality while working with state-of-the-art analytical equipment in a GMP environment. You'll conduct testing of raw materials, in-process samples, and finished products using various analytical techniques, evaluate test data, document results, and participate in continuous improvement initiatives. This role offers excellent opportunities for professional growth while working alongside colleagues who share your commitment to science and quality.

Position Summary

As QC Chemist, you will ensure that Quality control operations meet cGMP and Regulatory compliance and Data Integrity principals while respecting regulations, corporate standards and clients' requirements.

This role is responsible for method transfer/verification/validation of methodology, and project work within the department to support manufacture and release of pharmaceutical raw materials, intermediates and products. The role contributes to building and maintaining QC lab cGMP system, delivers analytical solution to clients through expertise in specific method qualification and validation strategies while ensuring timely delivery for projects.

Responsibilities

To perform transfer/verification/validation of laboratory procedures within the team where required

To prepare technical documentation including but not limited to protocols, analytical write-ups, standard operating procedures, specifications and reports

To perform analysis of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies

To review analytical and laboratory data within the department for accuracy, completeness and compliance with documented procedures

To perform write up for laboratory investigations, deviation and on time closure in line with Quality Management system procedures

Management of QC chemical, reference standard and consumable stock levels

To communicate effectively with others on site and internationally, and to participate with them in problem solving activities

Participate/contribute in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab

Support and encourage a "Quality Culture" and company 4i values throughout QC

Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business

Undertake ad-hoc activities that may be required by the business

Minimum Requirements/Qualifications

Degree in Chemistry or strongly related scientific discipline

At least 3 years relevant industrial experience

Ability to apply GMP regulations and other international guidelines to all aspects of the position

Ability to work independently and adhere to critical timelines

Effective communication skills at all internal and external levels

Excellent attention to detail