JOB DESCRIPTION

When you’re part of the team at Thermo Fisher, 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 real-world impact, and you’ll be supported in achieving your career goals.
Be on the front lines of delivering impactful pharmaceutical products to patients! This Quality Assurance Technician role is responsible for ensuring our clinical trials packaging products are manufactured at the highest standards of quality and compliance. Make a difference!

Responsibilities:

• Applies Good Manufacturing Practices (cGMP) in all areas of responsibility and follows all Thermo Fisher Standard operating procedures.
• Performs process inspections, samplings, and audits. Assures that issues potentially affecting product quality/compliance are escalated to the attention of the Team Leader and/or Management.
• Performs incoming inspections on material (drug, components, etc.) and distribution shipments.
• Performs approval of specifications (drug, components, etc.)
• Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues.
• Assures that issues are resolved in a timely manner and corrective actions are implemented accordingly.
• Other duties may be assigned to meet business needs.

Minimum Qualifications:

• Knowledge or prior experience with Current Good Manufacturing Practices (cGMP) for pharmaceutical products.
• Associate’s degree preferred and/or equivalent years of experience, with minimum of 1-2 years in Pharmaceutical or of a related, regulated industry.
• Must be able to work in an ambient, refrigerated, or freezer environments or potent compound suites with provided personal protective equipment (PPE).
• Good reasoning and problem-solving skills, prioritization, basic math skills, good communication skills, basic computer skills.
• Must be willing to work various shifts and overtime depending on business needs.
• Must be able to work independently.
• Must not be allergic to penicillin or cephalosporin products.
• Extensive standing and walking on packaging floor in order to monitor room activities.
• The employee must occasionally lift and/or move up to 20 pounds.
• Proficient in Microsoft Office including Word, Excel, Access, and Outlook.

At Thermo Fisher Scientific, each one of our 100,000+ extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer. Apply today http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

• Applies Good Manufacturing Practices (cGMP) in all areas of responsibility and follows all Thermo Fisher Standard operating procedures.
• Performs process inspections, samplings, and audits. Assures that issues potentially affecting product quality/compliance are escalated to the attention of the Team Leader and/or Management.
• Performs incoming inspections on material (drug, components, etc.) and distribution shipments.
• Performs approval of specifications (drug, components, etc.)
• Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues.
• Assures that issues are resolved in a timely manner and corrective actions are implemented accordingly.
• Other duties may be assigned to meet business needs