In Process Inspector 2 - Finishing Operations, 3rd Shift

Work Schedule Third Shift (Nights) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift,

Warehouse Job Description Shift Schedule:

3rd Shift 11:00pm

• 07:30am

Pay Range:

$24

• 26 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.

Education:

High school diploma or equivalent required.

Experience:

Required:

Minimum of 2 years of work experience in QA or QC or related field

Preferred:

Experience in a cGMP environment or

QA & QC Knowledge, Skills, Abilities:

Knowledge of automatic inspection equipment: Possesses a solid understanding of the operation and uses automatic inspection equipment specific to pharmaceutical labeling manufacturing. Capable of setting up and calibrating equipment, interprets, and analyses inspection results, and troubleshoots any equipment-related issues. Familiarity with automatic inspection equipment and its capabilities is crucial for effective quality control. Ability to follow pacing and maintain production flow: Possesses the ability to follow pacing and maintains the production flow including effectively managing their time, ensuring inspections are conducted in a timely manner, and keeping up with the production schedule. Maintains attention to detail to prevent any bottlenecks in the manufacturing process.

Problem tracking and troubleshooting skills:

Possesses strong problem tracking and troubleshooting skills and the ability to identify and track issues or deviations during inspections. Investigates root causes, and propose appropriate corrective actions. Applies analytical thinking and problem-solving abilities to address quality-related problems promptly and effectively. Maintains quality standards, minimizes disruptions, and ensures smooth operations in pharmaceutical trial labeling manufacturing. Physical Requirements / Work Environment Fast-paced environment which relies on teamwork to ensure jobs are completed within established timelines. What We Offer 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 Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values

• Integrity, Intensity, Innovation and Involvement
• working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Compensation and Benefits The hourly pay range estimated for this position based in New York is $21.82
• 32.

72. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: 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 For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. 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. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.