Microbiologist I (Normal Office Hours initially | Future 12 Rotating Shift Opportunity)

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Be part of our Quality Control team at Thermo Fisher Scientific where youll contribute by ensuring the quality and reliability of products that help make the world healthier cleaner and safer. Youll perform testing and analysis to support the development of innovative therapeutic products. Youll conduct quality control testing of raw materials in-process samples and finished products using various analytical techniques. Youll document and analyze test results participate in investigations and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.

JOB RESPONSIBILITIES

• Perform quality control microbiological testing of raw materials incoming goods intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.

• Participate in method transfer verification and validation for new product introductions.

• Conduct monitoring for facilitys utilities systems.

• Support equipment qualification processes.

• Perform and coordinate calibration and maintenance of laboratory equipment.

• Assist in aseptic process simulations.

• Conduct periodic reviews or preparation of new laboratory documents.

• Lead microbiological inventory required for testing.

• Ensure accuracy completeness and compliance of laboratory data.

• Maintain individual training records.

• Engage in continuous improvement activities.

• Strictly adhere to cGMP in your area of work.

• Maintain a 5S approach to HSE and cGMP.

• Carry out additional tasks as required by the reporting Manager.

• Support shift work when necessary.

• Understand and follow emergency procedures and safe work systems.

• Ensure compliance with environment health safety and security policies and procedures rules signage and instructions at all times.

• Report and investigate accidents near misses and rule breaches promptly.

REQUIREMENTS:
Bachelors degree 1-2 years experience in quality control laboratory environment preferably in pharmaceutical/biotech industry
Preferred Fields of Study: Microbiology Biotechnology Biology or related scientific field
Strong knowledge of cGMP GLP and quality management systems
Experience with microbiological testing methods and aseptic techniques
Ability to follow SOPs and maintain detailed documentation per GDP requirements
Strong computer skills including LIMS Microsoft Office and analytical software
Excellent attention to detail and organizational skills
Strong analytical and problem-solving capabilities
Ability to work both independently and collaboratively in a team environment
Clear written and verbal communication skills
Experience with laboratory equipment maintenance and calibration
Knowledge of relevant pharmacopeia standards and regulatory requirements
Ability to manage multiple priorities effectively
Flexible scheduling may be required
Physical ability to perform laboratory work including PPE usage