quality lab technician

Kraft Heinz

<div><h2 class="jobSectionHeader">Job Description
</h2><div></div><div><div><div><div><div><div><div><div><div>Job Purpose
This role supports the implementation and execution of key food safety microbiological and analytical testing by performing routine quality control activities, and executing testing using approved microbiological and analytical methods to support food safety and quality. The position works on site in the laboratory and on the production floor to perform sampling for routine environmental and product testing.
Essential Functions &amp; Responsibilities
<ul><li>Support testing completion through media preparation, quality control activities, sample collection, and execution of microbial testing on daily basis.
</li><li>Support and execute sanitation verification testing, shelf-life studies and other microbiological testing to verify critical limits for critical processes.
</li><li>Partner with internal business partners to update/maintain and improve laboratory standards and procedures.
</li><li>Maintain excellent records of laboratory equipment and testing performed.
</li><li>Perform testing, evaluate and approve microbiological test results for the Kraft Heinz network.
</li><li>Participate in proficiency testing program and internal laboratory audit process for internal factory laboratories.
</li><li>Support sanitation verification, validation of pre-requisite programs and HACCP preventive controls (cooking, formulation, etc.) through routine product and environmental sampling and testing.
</li><li>Remain current in scientific and regulatory principles of food safety to ensure most relevant information and emerging issues are identified and incorporated into Kraft Heinz food safety programs.
</li><li>Perform administrative tasks such as managing inventory, ordering of lab supplies, and data entry.
</li><li>Perform cross-functional communication of results with internally generated data.
</li><li>Other duties as assigned.
</li></ul>Expected Experience &amp; Required Skills
<ul><li>Past experience performing relevant food safety or analytical science work in a laboratory required (1-3 years preferred).
</li><li>Knowledge and experience of GLPs (Good Laboratory Practices) required, including routine handling of BSL2 organisms.
</li><li>Knowledge and experience of GMPs (Good Manufacturing Practices) preferred.
</li><li>Experience with LIMS (Laboratory Management Systems) and data management preferred.
</li><li>Experience performing microbiology laboratory techniques and analytical chemistry procedures, including rapid test methods.
</li><li>Awareness of quality management systems/processes (ISO, Six Sigma etc.), especially ISO 17025 requirements.
</li><li>Work experience in team-oriented functions as well as individual contribution.
</li><li>Must be able to work assigned shift with prompt and regular attendance, weekends or overtime as needed.
</li><li>Strong technical, communication and organizational skills required.
</li><li>Detailed-oriented.
</li><li>Effective communication skills (oral, written and verbal).
</li><li>Planning and organizational skills.
</li><li>Ability to walk, sit, stand, climb, work near moving equipment, occasionally lift up to 25lbs, operate a computer, keyboard/typing, communicate in-person and via telephone, complete paperwork responsibilities.
</li></ul>Work Environment &amp; Schedule
This position is considered a Manufacturing plant environment with heavy machinery and equipment. Additionally, this role requires extended hours as needed in the lab.
This is a Monday -Thursday shift starting at 5pm.
Physical Requirements
Physical demands include but not limited to
<ul><li>Frequent activity or conditions sustained 1/3 to 2/3 of working hours; upright stance, keyboard or text input; sedentary &ndash; occasionally exerting 0-10 lbs. of force, limited movement from workstation for brief period of time.
</li></ul>This job description is not designed to cover or contain all duties or responsibilities that are required of the role. Duties or responsibilities may change or be added with or without notice.
</div></div></div></div></div></div></div></div></div>Our Total Rewards philosophy is to provide a meaningful and flexible spectrum of programs that equitably support our diverse workforce and their families and complement Kraft Heinz&rsquo; strategy and values.
New Hire Base Salary Range:
$56,800.00 - $71,000.00
Bonus: This position is eligible for a performance-based bonus as provided by the plan terms and governing documents.
The compensation offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors
Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family&rsquo;s needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.
Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families.
You&rsquo;ll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example:
<ul><li>Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments
</li><li>Social - Paid Time Off, Company Holidays, Leave of Absence, Flexible Work Arrangements, Recognition, Training
</li><li>Emotional &ndash; Employee Assistance Program , Wellbeing Programs, Family Support Programs
</li><li>Financial &ndash; 401k, Life, Accidental Death &amp; Dismemberment, Disability
</li></ul>Location(s)
Davenport Plant (New) 
 
Kraft Heinz is an Equal Opportunity Employer &ndash; Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes. In order to ensure reasonable accommodation for protected individuals, applicants that require accommodation in the job application process may contact NAZTAOps@kraftheinz.com for assistance.</div>

Quality Lab Technician

Kendall Packaging

<div>About us
Kendall Packaging Corporation is the preferred flexible packaging manufacturer and on-time industry leader for custom-manufactured barrier needs.
Kendall Packaging Offers:<ul><li>
Competitive Wages</li><li>
Comprehensive Benefits Package</li><li>
Increased Off-Shift Premiums $3.00</li><li>
Three (3) - Paid Sick Days</li><li>
Ten (10) - Paid Holidays</li><li>
Four (4) Hours - Paid Volunteer Time Off</li><li>
401(k) Profit Sharing Match</li><li>
Access to On-Site Fitness Center &amp; Personal Trainer</li><li>
Climate Controlled Work Environment</li></ul>
ESSENTIAL DUTIES AND RESPONSIBILITIES include, but are not limited to the following:<ul><li>
Assist with inspection of jobs from presses, laminator, and slitter to confirm colors, adhesives, bonding, film size, thickness, and other parameters meet customer specifications.</li><li>
Assist in evaluating product quality to ensure compliance with both customer requirements and company quality standards.</li><li>
Assist in notifying appropriate personnel when inspection data exceeds acceptable limits or when significant quality issues are identified; support implementation of corrective actions.</li><li>
Assist in verifying that UPC codes are readable and compliant.</li><li>
Assist in organizing, maintaining, and completing all required documentation and records, including Certificates of Analysis, related to product quality and production jobs.</li><li>
Follow all cleanup and housekeeping procedures; comply with all quality, safety, and sanitation regulations.</li><li>
Organize and maintain the sample program and sample inventory.</li><li>
Perform quality checks on samples produced from each production department.</li><li>
Adhere to all GMP policies and procedures.</li></ul>
QUALIFICATION REQUIREMENTS: 
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION AND/OR EXPERIENCE: 
Requires education generally equivalent to a high school diploma, and three to twelve months related experience to become familiar with equipment and processes.
LANGUAGE SKILLS: 
Ability to read and comprehend simple instructions, short correspondence, and memos. Ability to write simple correspondence. Ability to effectively present information in one-on-one and small group situations.
MATHEMATICAL SKILLS: 
Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio and percent.
OTHER SKILLS AND ABILITIES: 
Requires the ability to operate a slitter machine, to operate a forklift truck, hand trucks, a hoist and hand jacks, and the ability to operate a variety of small hand tools.
PHYSICAL DEMANDS: 
While performing the duties of this job, the employee is regularly required to stand. The employee frequently is required to walk; use hands to finger, handle, or touch objects, tools, or controls; reach above shoulders; and talk or hear. The employee is occasionally required to climb or balance; stoop, kneel, crouch, or crawl; taste or smell; and use foot/feet to operate machine. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
WORK ENVIRONMENT: 
While performing the duties of this job, the employee regularly works near moving mechanical parts and is regularly exposed to fumes or airborne particles. The employee occasionally works in high, precarious places and is occasionally exposed to toxic or caustic chemicals and risk of electrical shock.</div>

Quality Lab Technician Assistant - 3rd Shift

Schreiber Foods

<div><h1 class="jobSectionHeader">Job Category:
</h1>Quality
<h1 class="jobSectionHeader">Job Family:
</h1>Plant Quality Assurance
<h1 class="jobSectionHeader">Work Shift:
</h1><h1 class="jobSectionHeader">Job Description:
</h1>Rotating 12-hour Night shifts
Pay Scale
Entry Level-$22.59
24 months-$27.74
Position Purpose: Responsible for completing all lab analysis to ensure quality and productivity is maintained. Directly involved in the production process. 
Must follow Good Manufacturing Practices and good housekeeping guidelines. Must follow safety guidelines, wear designated Personal Protective Equipment and meet OSHA safety requirements.
Essential Functions
<ul><li>Daily performance of laboratory tests on cheese and ingredients.
</li><li>Equipment used includes but not limited to microwave ovens, pH meter, analytical and technical balances, magnetized hot salts, calculator, CRT terminal, and various types of glassware and utensils.
</li><li>Maintain work area in an approved housekeeping/sanitary condition.
</li><li>Will be involved using TPM and QIP.
</li><li>Expectation that approximately 70% of work time will be spent on production floor.
</li><li>Must be able to read and write English
</li><li>Preform an assignment ask by leaders.
</li><li>Regular attendance
</li></ul>SKILLS:
<ul><li>Must be capable of learning and performing various laboratory tests with sensitive instruments and equipment.
</li><li>Must be capable of operating or learning to operate a calculator or CRT terminal to compute test results and/or input data.
</li><li>Must be capable of reading fine graduation on the test bottles and equipment.
</li><li>Must be willing to accept responsibility.
</li><li>Must be willing to learn new process systems as they evolve.
</li><li>Must be able to work overtime as needed.
</li><li>Must be able to develop, use, and control the process controls in all areas of the plant.
</li><li>Must be responsible for printing the summary management audits for the shift.
</li><li>Must be able to work around ammonia systems, acid systems, steam systems, and high voltage.
</li><li>Must be able to wear all required PPE including but not limited to safety shoes, hairnet, and hard hat at all times.
</li><li>Must be able to wear gloves, goggles, face shield, ear protection, and/or gars mask as the need arises.
</li><li>Must be able to perform simple math, read and write English.
</li></ul>PHYSICAL DEMANDS ANALYSIS:
 Stand
 Walk
 Sit
 Crouch
 Climb
 Prone and/or overhead
 Lift/Carry up to 50 pounds
<h1 class="jobSectionHeader">Eligible partners will receive:
</h1><ul><li>A 401(k) plan that includes up to an 8 percent Schreiber match and has been recognized as Best-in-Class for companies with 5,000-plus employees.
</li><li>Competitive medical, prescription drug, dental and vision benefits without a waiting period, including second-opinion medical consultation with specialists
</li><li>Wellness resources, including a fitness reimbursement program and access to an interactive personalized online wellness program
</li><li>Paid vacation and holidays
</li><li>Professional growth and development opportunities through training and our Education Assistance Program
</li><li>Childcare costs . Get up to $5,000 annually to help you with the cost of childcare. Monthly contributions toward childcare expenses, including independent babysitters.
</li></ul>Schreiber requires that an employee have authorization to work in the country in which the role is based. In the event, an applicant does not have current work authorization, Schreiber will determine, in its sole discretion, whether to sponsor an individual for work authorization. However, based on immigration requirements, not all roles are suitable for sponsorship.
An Equal Opportunity Employer, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Want to be alerted of new openings? Sign in and click the Job Alerts button in the upper-right corner to create a job alert.</div>

Quality Assurance Lab Technician | 12-hour night shifts | Starting at $22.59/hr, reaching $27.74/hr after 24 months

Pacific Coast Producers

<div>Pacific Coast Producers, a growing agricultural cooperative with food production facilities across the West Coast, is seeking a talented and experienced Quality Control Lab Lead to join our team at our Production Facility in The Dalles, OR. PCP is investing in its people and advancing a culture of service, where each employee can do their best to make affordable, high-quality food for customers across North America. Our Salem facility produces maraschino cherries and other cherry products in various styles, colors, and flavors. 
 
Hours of Operation: Full time/ 40 hours per week with some weekend and overtime hours required when needed, possible day or swing shift position. This position is part of a seniority based Collective Bargaining Unit (CBA) and requires work on various shifts.
Join our legacy of talented people working together to provide the highest level of customer service. PCP employees receive terrific benefit plans such as affordable medical, dental, and vision insurance. Retirement savings plans, including a defined-benefit pension plan is also provided to eligible employees.
Pay: $27.26 / hour
Overview
The QC Lab Lead will be responsible for overseeing lab staff duties and Quality Control (QC) record keeping. Direct, train and monitor graders, lab techs and pit checkers in all areas of production.
Primary Duties<ul><li>
Maintain current knowledge of grades and specifications of all areas of production.</li><li>
Check, evaluate, review, maintain and update accurate QC documentation, forms, logs and procedures.</li><li>
Proficient in grading with the ability to direct, train and monitor QC graders &amp; lab techs.</li><li>
Perform routine laboratory tests, maintain laboratory equipment and supplies.</li><li>
Frequent use of computers and programs to lookup, enter, monitor, analyze and evaluate data. Create reports and documentation.</li><li>
Enter QC data into computer in a timely manner.</li><li>
Perform, direct and evaluate microbiological testing.</li><li>
Oversee sample request ordering, preparations, labeling, entry and shipping.</li><li>
Maintain a clean, organized and hazard free work area.</li><li>
Perform other duties as may be assigned by the QA Manager.</li><li>
Maintain confidentiality on results obtained from in house or third-party testing.</li><li>
Pacific Coast Producers. is a food processing facility, and it is the responsibility of every employee to perform all job duties and other activities in a manner that upholds the safety and quality of the facilities and products produced. In addition, it is the responsibility of each employee to report all food safety issues or concerns to a Production Manager, Plant Manager or QA Manager.</li></ul> 
Minimum Qualifications<ul><li>
Associates degree in physical science; or 2 years of lab experience in lieu of degree.</li><li>
Proficient in Excel, Microsoft Word, Outlook and general computer skills</li><li>
Strong arithmetic skills (must be able to calculate percentages, ppm, averages, basic addition, subtraction, multiplication and division).</li><li>
Must have laboratory skills (measuring pH, titrating, solutions preparation, laboratory cleaning, and laboratory safety).</li><li>
High degree of cleanliness and organization.</li><li>
Ability to work well with and motivate others and be a self-starter.</li><li>
Must be able to work within deadlines and time restraints.</li><li>
Exercise care and attention in the performing of daily duties as reports are relied on as the accurate record of product quality.</li><li>
Excellent verbal, written and interpersonal communication skills. Must be able to read and write English.</li><li>
Demonstrates ability to follow all good manufacturing practices and safety rules.</li><li>
Must have and maintain a good attendance record and performance record.</li><li>
Be able to become PCQI certified.</li></ul> 
Physical Requirements 
Frequent physical activity includes walking, bending, standing, twisting, pushing, pulling, lifting, and carrying up to 50 lbs., touching, reaching, gripping, finger dexterity, and hearing. Moderate physical activity may include stooping, color identification, close vision, and depth perception. Under strenuous conditions, employees are still expected to perform their job requirements in a safe manner. 
 
Environmental Factors 
Working conditions include exposure to plant temperature extremes, dampness, humidity, fumes, and high noise levels. Work requires wearing proper protective equipment. Incumbent may work in a crowded area. 
 
Note &ndash; Employees are expected to comply with all applicable Company rules and policies, as well as the guidelines that apply to their specific position. It is the responsibility of every employee to perform all job duties and other activities in compliance with customer, 3rd party, regulatory, and company food safety and quality initiatives and standards. In addition, it is the responsibility of each employee to report all food and employee safety issues or concerns to management.</div>

QC Lab Lead

Eli Lilly

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
Organization Overview:
Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN (Lilly Lebanon API). This facility is Lilly&rsquo;s largest investment in manufacturing capacity and is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the startup team for the manufacturing site, and the successful candidate will help to build the processes and facility to enable a successful startup into GMP manufacturing operations.
Position Description:
The technician position participates in environmental and utilities monitoring for all site buildings following procedurally required frequencies. This role may include performing aseptic testing, incubation and analysis of environmental monitoring samples.
Key Objectives/Deliverables:<ul><li>
Perform environmental monitoring sampling, including non-viable, viable, surface sampling and personnel monitoring in the various site manufacturing and support facilities.</li><li>
Perform utility sampling, including non-viable, viable, oil content, dew point, and purity on compressed gas systems.</li><li>
Perform sampling on water systems.</li><li>
Participate in performance qualification of environmental, utility, and water systems.</li><li>
Perform data entry and review work for accuracy in accordance with laboratory procedures, standards, and GMP requirements.</li><li>
Train others within the lab, as required.</li><li>
Perform routine equipment qualifications/calibrations or maintenance through execution of well-defined protocols, as required.</li><li>
Troubleshoot equipment and methods, as required.</li><li>
Ensure complete and effective monitoring data using electronic systems.</li><li>
Ensure that data integrity is maintained.</li><li>
Second Person Verify (SPV) data of other technicians, as required.</li><li>
Ensure compliance with current Good Manufacturing Practices (cGMPs) and assist in identification and investigations of non-conformance issues.</li><li>
Recognize deviations from procedures and initiate investigations.</li><li>
Execute notifications to management when required by procedures or standards.</li><li>
Responsible for maintaining a safe work environment, working safely and being accountable for supporting all HSE Corporate and Site Goals.</li><li>
Support a constant state of inspection-readiness.</li><li>
Continuous Improvement Initiatives:</li><li>
Identify and communicate opportunities for improvement initiatives in daily work activities.</li><li>
Follow Lilly standards for CCI/Lean and support departmental or site continuous improvement initiatives.</li></ul>
Basic Requirements:<ul><li>
Associate degree (2 year) in a science field such as microbiology or biology or High School Diploma with 2 years of relevant GMP experience.</li><li>
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.</li></ul>
Additional Preferences:<ul><li>
Ability to work in a highly regulated lab environment, including wearing appropriate PPE and using other safety-required equipment.</li><li>
Understanding of cGMPs, environmental monitoring procedures, processes, and equipment.</li><li>
Strong skills in: written and oral communication, troubleshooting and investigative work, and critical thinking and decision-making.</li><li>
High attention to detail and the capability of meeting critical deadlines by organizing and prioritizing multiple tasks.</li><li>
Proficiency with computer systems, including instrument-specific applications and Microsoft Office products.</li></ul>
Other Information:<ul><li>
Role may be in support of 24-hour operations, requiring shifts that cover days, nights, and weekends.</li><li>
Overtime, as needed, and must be available off-shift to respond to operational issues.</li><li>
Tasks may require repetitive motion and standing for long periods of time.</li><li>
Must be able to lift at least 30 pounds.</li></ul>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. 
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
$18.02 - $34.90
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly</div>

Technician – QC Lab - Lebanon

Kindeva Drug Delivery

Our Work Matters
 At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
 
The Impact You Will Make
 Kindeva Northridge is currently seeking a meticulous and detail-oriented Quality Control Laboratory Technician to join our team. The Quality Control Laboratory Technician will play a crucial role in ensuring that our incoming Raw Material and Hard Goods meet quality standards and regulatory requirements. This position requires strong attention to detail, excellent organizational skills, and the ability to perform a variety of quality control tests and inspections. The ideal candidate will be dedicated to maintaining high standards of product quality and safety.
 
Role Responsibilities
 <ul>
<li>Perform routine Quality Control tests on hard goods and packaging components using standard testing methods and instrumentation. Conduct tests to assess product quality and compliance with specifications.</li>
<li>Ensure that samples are properly labeled, handled, and stored to maintain sample integrity and traceability.</li>
<li>Operate laboratory equipment and instrumentation used for Quality Control testing, including spectrophotometers, pH meters, balances, and other analytical instruments. Follow Standard Operating Procedures (SOPs), Work Instruction (WI) and safety protocols for instrument operation.</li>
<li>Record test results, observations, and other relevant data accurately and legibly in laboratory notebooks, worksheets and/or electronic databases. Maintain detailed records of all Quality Control activities in compliance with regulatory requirements and Kindeva policies.</li>
<li>Communicate all non-conformances or atypical results to Quality Control Group Lead and/or Manager in a timely manner.</li>
<li>Document non-conformance in Quality Management System as required.</li>
<li>Support continuous improvement activities within functional group and/or department as needed.</li>
<li>Adhere to all safety regulations and Kindeva policies related to laboratory operations and quality control testing. Follow established protocols for handling hazardous materials, chemical waste disposal, and personal protective equipment (PPE) usage.</li>
<li>Comply with GMPs and department SOPs.</li>
<li>Update or Create documents such as SOPs, WIs or Worksheet/Forms as needed to update or document new procedures.</li>
<li>Work well in both a team and an individual environment.</li>
<li>Maintain flexibility to support unexpected rush material release requests.</li>
</ul>
Basic Qualifications
 <ul>
<li>High school diploma or equivalent required.</li>
<li>Minimum 3 years of experience in a Quality Control or Laboratory Technician role within a manufacturing environment.</li>
<li>Strong attention to detail and ability to follow written and verbal instructions accurately.</li>
<li>Proficiency in basic mathematical calculations and measurement techniques.</li>
<li>Commitment to maintaining a safe work environment and complying with regulatory requirements.</li>
<li>Ability to prioritize and manage multiple assignments while maintaining strong attention to detail</li>
<li>Excellent planning and organization skills required for our fast-paced environment and must be highly motivated, proactive and willing to take on new challenges.</li>
</ul>
Preferred Qualifications
 <ul>
<li>Associate degree or certification in a scientific field.</li>
</ul>
#LI-Onsite
 
California residents should review our Notice for California Employees and Applicants before applying.
 
The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits, etc.).
 
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
 
Equal Opportunity Employer: 
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
 
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

QC Raw Materials Lab Technician

Share Corporation

<div>QA/QC Laboratory Technician 
Job Summary: 
 We are seeking a QA/QC Laboratory Technician to perform chemical and physical laboratory tests, providing support to R&amp;D, Production, and external partners. The role involves conducting qualitative and quantitative analyses of solids and liquids in work-in-progress and final products. 
Qualifications:<ul><li>
Two-year associate degree/certificate in a scientific field, ideally chemistry, or equivalent experience.</li><li>
2&ndash;5 years in a laboratory within a manufacturing environment.</li><li>
Proficiency in basic computer programs (Excel, Word, Outlook).</li><li>
Experience with ERP systems (SAP experience preferred).</li><li>
Strong math skills, including unit conversions and multi-step calculations.</li><li>
Strong organizational skills and the ability to manage multiple tasks.</li><li>
Excellent attention to detail, communication skills, and ability to work independently and in a team.</li><li>
A commitment to accuracy and quality in their work.</li><li>
A sense of urgency and responsibility in meeting deadlines.</li></ul> 
Primary Responsibilities:<ul><li>
Calibrate and maintain laboratory instrumentation.</li><li>
Analyze finished goods and raw materials.</li><li>
Prepare chemical reagents.</li><li>
Accurately input chemical and test results into a computer system.</li><li>
Create and prepare Certificates of Analysis (COAs) for customers.</li><li>
Verify and document specialty outbound products</li><li>
Review and audit production activities such as filling and mixing operations.</li><li>
Perform document checks, measurements, and weight verifications during line reviews and audits to ensure adherence to specifications.</li><li>
Manage retained samples of finished products and raw materials.</li><li>
Write simple observation-based reports.</li><li>
Apply knowledge of long-term stability standards (preferred but not required).</li><li>
Collaborate and communicate effectively with internal and external customers.</li><li>
Assist with other laboratory tasks as assigned.</li></ul></div>

QA/QC LAB TECHNICIAN

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