In Process Inspector - Press Manufacturing - 3rd Shift
About The Position
As part of the Thermo Fisher Scientific team, you’ll 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 world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: Clinical Labeling Services, part of the Clinical Trials Division, located in Bohemia, New York provides leading clinical label design, production and management services for the pharmaceutical and biotechnology industry. Our advanced inspection software, full in-house print capabilities, and proprietary translation and regulatory approval system are designed to reduce overall clinical trial label cycle times How Will You Make an Impact?: The QC Technician II plays a crucial role in ensuring the quality and accuracy of labeling materials used in clinical trials. They are responsible for conducting inspections to verify compliance with regulatory requirements and internal standards. Their attention to detail and adherence to quality control procedures significantly impact the overall efficiency and safety of the manufacturing process A Day in the Life: Conduct thorough inspections: Responsible for performing inspections and tests on raw materials, in-process samples (startups), and finished products. Follows established protocols and applies various analytical techniques to ensure compliance with quality standards and regulatory requirements. Document and report findings: Accurately records and documents all inspection and test results. Effectively communicating findings is crucial for maintaining traceability and facilitating corrective actions. Ensuring adherence to quality control procedures: Ensures that all quality control procedures and protocols are followed consistently including monitoring and verifying compliance with standard operating procedures (SOPs), safety guidelines, and regulatory requirements
Requirements
- High school diploma or equivalent required.
- Minimum of 1 year of work experience in QA or QC or related field
- Strong understanding of quality control principles and practices: Possesses a comprehensive knowledge of quality control principles, methodologies, and standard processes.
- Understands inspection techniques, and relevant paperwork procedures.
- Familiar with quality control tools and able to interpret and analyse data effectively.
- Attention to detail and accuracy: Pays close attention to detail and maintains accuracy.
- Possesses a meticulous approach to their work, ensures that all inspections, tests, and documentation are completed with precision including the ability to identify and document deviations or non-conformities accurately, as well as the skill to spot potential quality issues and take appropriate actions.
- Effective communication and documentation skills: Possesses excellent communication skills, both written and verbal.
- Communicates' findings, observations, and recommendations clearly and concisely to colleagues, supervisors, and other team members.
- Accurately records and maintains detailed reports, logbooks, and other quality control records.
- Ensures proper traceability and facilitates effective communication within the organization.
Nice To Haves
- Experience in a cGMP environment
Responsibilities
- Conduct thorough inspections: Responsible for performing inspections and tests on raw materials, in-process samples (startups), and finished products.
- Follows established protocols and applies various analytical techniques to ensure compliance with quality standards and regulatory requirements.
- Document and report findings: Accurately records and documents all inspection and test results.
- Effectively communicating findings is crucial for maintaining traceability and facilitating corrective actions.
- Ensuring adherence to quality control procedures: Ensures that all quality control procedures and protocols are followed consistently including monitoring and verifying compliance with standard operating procedures (SOPs), safety guidelines, and regulatory requirements
Benefits
- Competitive Hourly Pay Rate
- Additional shift differential for 2nd shift and 3rd shift positions
- Annual performance-based bonus
- Annual merit performance-based increase
- Excellent Benefits
- Benefits & Total Rewards | Thermo Fisher Scientific
- Medical, Dental, & Vision benefits-effective Day 1
- Paid Time Off & Designated Paid Holidays
- Retirement Savings Plan
- Tuition Reimbursement
- Employee Referral Bonus
- Career Advancement Opportunities
- A choice of national medical and dental plans, and a national vision plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
