In Process Inspector 2 - Finishing Operations, 2nd Shift
About The Position
The In Process Inspector role has a significant impact in ensuring the quality and integrity of the production process. Their responsibilities include monitoring and inspecting the various stages of manufacturing to identify any discrepancies while using automatic equipment or visually inspecting labels. Their vigilance and attention to detail play a crucial role in preventing defects, ensuring product safety, and maintaining overall process efficiency. A Day in the Life: Conducting inspections using automatic inspection equipment: Operates and monitors automatic inspection equipment to assess the quality and integrity of pharmaceutical labels during the manufacturing process including setting up the equipment, conducting routine checks, and interpreting the results to identify any defects or change requests from specifications. Ensures that labels meet the required standards for accuracy, legibility, and adherence to regulatory requirements Performing QC inspections: Conducts Quality Control (QC) inspections at various stages of the manufacturing process including visually examining labels, verifying label content, conducting accurate counts, checking for proper alignment, and assessing print quality. Uses appropriate tools and techniques, to ensure that labels meet the necessary quality standards and complies with regulatory guidelines. Documenting and reporting findings: Records all inspection results and documents any non-conformities or deviations identified during the inspections including generating detailed reports, maintaining inspection records, and communicating findings to area supervisor or manager. Effective documentation and reporting facilitate traceability, support corrective actions, and contribute to the overall quality assurance process.
Requirements
- High school diploma or equivalent required
- Minimum of 2 years of work experience in QA or QC or related field
- Knowledge of automatic inspection equipment
- Ability to follow pacing and maintain production flow
- Problem tracking and troubleshooting skills
Nice To Haves
- Experience in a cGMP environment or QA & QC
Responsibilities
- Conducting inspections using automatic inspection equipment
- Performing QC inspections
- Documenting and reporting findings
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
Number of Employees
5,001-10,000 employees
