Manager, Quality Control
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Job Location:
High Point, NC - USA
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting OfficeJob 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.
Excellent Benefits Package
Review our companys Total Rewards
Medical Dental & Vision benefits-effective Day 1
Paid Time Off & Holidays
401K Company Match up to 6%
Tuition Reimbursement eligible after 90 days!
Employee Referral Bonus
Employee Discount Program
Recognition Program
Charitable Gift Matching
Company Paid Parental Leave
Career Advancement Opportunities
Location Information:
High Point NC
Click here for site video: High Point Softgels
Essential Duties and Responsibilities
- Ensures that the QC laboratory is well-equipped with the necessary personnel to conduct timely testing of non-commercial and pre-commercial samples encompassing both process and cleaning validations.
- Provide mentorship and technical support to staff in troubleshooting instrumentation root cause analysis and implementing Corrective/Preventative Actions (CAPAs).
- Collaborate with internal and external customers to support site and company initiatives.
- Uphold and implement safety regulations and company policies.
- Conduct regular 1-on-1 mentoring sessions and annual performance evaluations for team members.
- Represent Quality Control during audits and regulatory inspections.
Qualifications
- BS degree with 8 years of laboratory experience preferably within a cGMP pharmaceutical laboratory environment including 2-3 years of supervisory experience.
- Meet applicable DEA security clearance requirements.
- Skilled in the interpretation of guidelines and employing rational or scientific reasoning.
- Proficiency in operating basic and complex laboratory equipment and software such as Empower Chromeleon MS Word and Excel.
Required Experience:
Manager
Key Skills
- Laboratory Experience
- Quality Assurance
- Construction Experience
- FDA Regulations
- ISO 9001
- Assays
- Quality Systems
- Quality Control
- Quality Management
- cGMP
- QA/QC
- HACCP
About Company
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
