Work Schedule
Second Shift (Afternoons)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed No contact lens allowed; prescriptive glasses will be provided Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)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.
*FIXED TERM CONTRACT - 18 - Month Contract *
Shift:
Tuesday - Saturday
3:30 pm 11:30 pm
DESCRIPTION:
At Thermo Fisher Scientific youll join a quality assurance team focused on ensuring consistent execution of quality standards and regulatory compliance. Youll play a vital role in enabling our customers to make breakthrough discoveries and innovations that make the world healthier cleaner and safer. Youll ensure product quality drive continuous improvement initiatives and collaborate with cross-functional teams to maintain the highest standards of quality and compliance in a GMP environment.
REQUIREMENTS:
- Relevant batch review/documentation experience preferred
Additional certifications in Quality Systems or GMP preferred
Strong knowledge of cGMP ISO standards (13485/9001) and international regulatory requirements
Experience with quality systems and documentation including batch records SOPs deviations CAPA
Proficiency in quality management software systems (TrackWise SAP etc.)
Demonstrated ability to perform detailed documentation review and quality assessments
Strong analytical and problem-solving skills for quality investigations and root cause analysis
Excellent written and verbal communication skills
Ability to work independently and collaborate effectively with cross-functional teams
Experience conducting internal quality audits and supporting external regulatory audits
Proficient computer skills including Microsoft Office applications
Strong attention to detail and commitment to accuracy
Ability to prioritize and adapt in a changing environment
Experience with continuous improvement methodologies (Lean Six Sigma) preferred
Must be able to work in controlled environments wearing required PPE
EDUCATION:
Bachelors Degree required. Experience in pharmaceutical medical device or regulated industry preferred
Preferred Fields of Study: Chemistry Biology Biotechnology Engineering or related scientific/technical field
Compensation
The salary range estimated for this position based in Canada is $46600.00$70000.00.Required Experience:
IC
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more