Clinical and Health - QC Technician

QC Technician – Entry Level

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment, or making sure our food is safe. Your work will have a real-world impact, and you'll be supported in achieving your career goals.

Location/Division Specific Information:
Clinical Trials Division (CTD) partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time – a concept that we internally accept as "There is a Patient Waiting." Our outstanding blend of services includes project management, packaging, distribution, transportation management and specialty logistics, ancillary supply management, clinical supply optimization, bio-repository storage and much more.

Our more than 3,000 employees in over 15 countries work hard every day knowing that what they do matters.

What will you do?

• Follows all Thermo Fisher SOPs (standard operating procedure) and performs job responsibilities in a safe and efficient manner.
• Performs process inspections, samplings, and audits
• Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues.
• Review production orders to verify all information is accurate per applicable reference documents and align with all customer requirements.
• Review/Approve label part number item specifications to guarantee the information contained within is accurate and stays in sync with requirements.
• Other duties may be assigned to meet business needs.

How will you get here?

Associates degree and/or equivalent work experience.

Experience:

Good reasoning and problem-solving skills, basic math skills, good interpersonal skills, basic digital literacy. 1-2 years experience in Pharmaceutical or of a related field, preferably in a regulated industry.

Knowledge, Skills, Abilities:
Ability to function in a dynamic environment and balance multiple priorities simultaneously. Experience with Quality Systems (Change Control, deviations, complaint management, documentation management, among others). Ability to work independently or as part of a team, self-motivated, adaptable. Proficient in Microsoft Office including Word, Excel, Access, and Outlook. Knowledge or prior experience with Current Good Manufacturing Practices (cGMP) for pharmaceutical products.