Sr. QA Technician (2nd Shift)

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for headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections if posting has real specific content. We need to parse the posting. Key info: - Work Schedule: Second Shift (Afternoons) Environmental Conditions Able to lift 40 lbs. without assistance, Office, Standing for full shift Shift: 2nd Shift 02:00pm - 10:30pm - Monday to Friday - Pay Range: $26.00 - $28.00 - Title: Sr. QA Technician - Description: As part of the Thermo Fisher Scientific team... (mission). How You Will Make an Impact: ... A Day in Life: bullet list of duties. - Education: High school diploma or equivalent required. - Experience: Minimum of 2 years of work experience in QA or QC or related field is required. Required: Experience in a cGMP environment - Knowledge, Skills, Abilities: list of items. - Physical Requirements / Work Environment: Fast-paced environment... Must be able to lift to 30 lbs., 13.6 kgs. Must be able to pack out clinical labels 20/40 corrected vision required, subject to bi-annual testing - Compensation: 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 - Also later: Compensation And Benefits: hourly pay range estimated for this position based in New York is $21.82–$36.36. 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 We need to remove boilerplate: cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. Also remove "Apply today!" and links. We need to preserve all substantive information. We need to decide sections: - About the role: maybe the mission paragraph and "As part of the Thermo Fisher Scientific team..." That's about role. - Responsibilities: the "How You Will Make an Impact:" and "A Day in Life:" bullet list. - Requirements: Education, Experience, Required: Experience in cGMP environment. - Qualifications: maybe combine with Requirements? But we can have Qualifications separate for knowledge, skills, abilities. - Skills: maybe the Knowledge, Skills, Abilities list. - Benefits: the benefits list. - Pay: the pay range and shift differential, bonus, etc. - Schedule: the shift details. We must not create sections with filler like "commensurate with experience". We have actual content. We need to use

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  . Responsibilities: The "How You Will Make an Impact:" paragraph and then the "A Day in Life:" bullet list. Let's capture: How You Will Make an Impact: As a Sr. Quality Assurance Technician, you will play a pivotal role in the overarching success of the Quality Operations team. The QA Operation team reviews and monitors all clinical labeling documentation, as well as performs final quality release of all clinical labels manufactured in our Bohemia, NY facility. With the support of department leadership, you will support the team by ensuring that all batch record documentation (a real time record of everything that is manufactured) has been verified and that products meet the form, fit, and function requirements of our clients to safely and successfully serve their patients’ needs. You will also support the packing of clinical labels to ensure safety. A Day in Life: Perform real-time verification of job documentation to ensure accuracy and completeness with a 24-hour turnaround time. Categorize and log all work performed in accordance with local procedures and regulatory requirements. Organize and maintain all batch records in clinical labeling custody including on-site storage and final archival. Perform pack out of clinical labels to ensure safe delivery to client/packaging sites. Participate in the PPI program by actively performing JDI and assisting with GEMBA We need to turn each sentence into

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    list. Qualifications: maybe not needed separate; but we have Knowledge, Skills, Abilities list. That could be Skills section. Skills: list of items: Strong understanding of quality assurance principles and practices... etc. Also includes Communication Skills, Technical Skills, Time Management, Multitasking, Adaptability, Collaboration. We'll make
    . Benefits: list: Medical, Dental, & Vision benefits-effective Day 1; Paid Time Off & Designated Paid Holidays; Retirement Savings Plan; Tuition Reimbursement; Employee Referral Bonus; Career Advancement Opportunities; plus later details: 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; 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. We need to avoid duplication. We'll combine unique items. Pay: Competitive Hourly Pay Rate; Additional shift differential for 2nd shift and 3rd shift positions; Annual performance-based bonus; Annual merit performance-based increase; Pay Range: $26.00 - $28.00; also later hourly pay range estimated for this position based in New York is $21.82–$36.36. There's some conflict; we need to preserve all substantive information, not invent or summarize away detail. So we should include both ranges? The posting includes both: earlier "Pay Range: $26.00 - $28.00" and later "Compensation And Benefits The hourly pay range estimated for this position based in New York is $21.82–$36.36." Both are substantive. We'll include both as separate statements maybe in

    . Schedule: Work Schedule Second Shift (Afternoons) Environmental Conditions Able to lift 40 lbs. without assistance, Office, Standing for full shift Shift: 2nd Shift 02:00pm - 10:30pm - Monday to Friday. Also physical requirements: Must be able to lift to 30 lbs., 13.6 kgs. Must be able to pack out clinical labels 20/40 corrected vision required, subject to bi-annual testing. Also Fast-paced environment which relies on teamwork to ensure jobs are completed within established timelines. We'll make Schedule section with

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      About the role

      ... (combined mission paragraphs)

      Responsibilities

      How You Will Make an Impact: As a Sr. Quality Assurance Technician, you will play a pivotal role in the overarching success of the Quality Operations team. The QA Operation team reviews and monitors all clinical labeling documentation, as well as performs final quality release of all clinical labels manufactured in our Bohemia, NY facility. With the support of department leadership, you will support the team by ensuring that all batch record documentation (a real time record of everything that is manufactured) has been verified and that products meet the form, fit, and function requirements of our clients to safely and successfully serve their patients’ needs. You will also support the packing of clinical labels to ensure safety.

      • Perform real-time verification of job documentation to ensure accuracy and completeness with a 24-hour turnaround time.
      • Categorize and log all work performed in accordance with local procedures and regulatory requirements.
      • Organize and maintain all batch records in clinical labeling custody including on-site storage and final archival.
      • Perform pack out of clinical labels to ensure safe delivery to client/packaging sites.
      • Participate in the PPI program by actively performing JDI and assisting with GEMBA.

      Requirements

      • High school diploma or equivalent required.
      • Minimum of 2 years of work experience in QA or QC or related field is required.
      • Experience in a cGMP environment is required.

      Skills

      • Strong understanding of quality assurance principles and practices: possesses comprehensive knowledge of QA principles, methodologies, and best practices; understands inspection techniques and relevant paperwork procedures; familiar with QC tools and able to interpret and analyze data effectively.
      • Attention to detail and accuracy: pays close attention to detail and maintains accuracy; meticulous approach; ensures documentation completed with precision; able to identify and document deviations or non-conformities accurately; spots potential quality issues and takes appropriate actions.
      • Effective communication and documentation skills: excellent written and verbal communication; communicates findings, observations, and recommendations clearly and concisely; accurately records and maintains detailed reports, logbooks, and other QC records; ensures proper traceability and facilitates effective communication.
      • Communication Skills: Strong verbal and written communication skills for reporting and collaboration.
      • Technical Skills: Proficiency with QA tools, software testing frameworks, and methodologies.
      • Time Management: Efficiently managing time to meet deadlines and project milestones.
      • Multitasking: Ability to handle multiple projects and tasks simultaneously.
      • Adaptability: Flexibility to adapt to changing requirements and environments.
      • Collaboration: Ability to work effectively with cross-functional teams including developers, product managers, and stakeholders.