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Associate Quality Control Analyst Jobs in Iowa (NOW HIRING)

The Quality Control Associates role will work in collaboration with the other associates to ensure coverage of the following responsibilities; check in of test samples from manufacturing to the QC ...

The Quality Control Associates role will work in collaboration with the other associates to ensure coverage of the following responsibilities; check in of test samples from manufacturing to the QC ...

The Associate QC Systems Specialist acts as the QC Systems (SAP, zLIMS, Binocs and other digital systems for QC) subject matter expert. Maintains compliance through creation and maintenance of ...

The Associate QC Systems Specialist acts as the QC Systems (SAP, zLIMS, Binocs and other digital systems for QC) subject matter expert. Maintains compliance through creation and maintenance of ...

The Associate QC Systems Specialist acts as the QC Systems (SAP, zLIMS, Binocs and other digital systems for QC) subject matter expert. Maintains compliance through creation and maintenance of ...

... analytical and IND enabling services. With over 40 years of experience and a team of 2,000 experts ... The QC Supervisor will be responsible for directing the laboratory workflow for daily testing of ...

Manages 4 departments within the Quality Control Organization, Virology; Bacteriology and ... Familiarity with statistical analysis and strong problem-solving skills * Strong technical writing ...

Manages 4 departments within the Quality Control Organization, Virology; Bacteriology and ... Familiarity with statistical analysis and strong problem-solving skills * Strong technical writing ...

Quality Control Technician

Carlisle, IA · On-site

$18.25 - $23.25/hr

Reports to: Quality Control Supervisor Position Summary: Inspect structural steel parts and ... Associates Degree in a technical field or higher preferred but not required. Experience: Two ...

... analysis, and initial set tests. * Inform Quality Control Manager of any nonconformity of product, personnel issues, or equipment issues. * Perform duties in a professional manner. * Work closely ...

Manages 4 departments within the Quality Control Organization, Virology; Bacteriology and ... Familiarity with statistical analysis and strong problem-solving skills * Strong technical writing ...

Quality Control Technician

Carlisle, IA

$18.25 - $23.25/hr

Quality Control Supervisor Position Summary: Inspect structural steel parts and assemblies during ... Associates Degree in a technical field or higher preferred but not required. Experience: Two ...

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Associate Quality Control Analyst information

What are some common challenges faced by associate quality control analysts during routine testing, and how can they be addressed?

Associate Quality Control Analysts often encounter challenges such as tight deadlines, managing multiple sample types, and handling complex analytical instruments. Staying organized and maintaining clear documentation helps manage workflow efficiently. Regular calibration and maintenance of laboratory equipment, along with ongoing training, are essential to minimize errors and ensure accurate results. Collaborating closely with senior analysts and cross-functional teams can also help troubleshoot unexpected issues and streamline processes.

What is the difference between Associate Quality Control Analyst vs Quality Control Technician?

AspectAssociate Quality Control AnalystQuality Control Technician
CredentialsBachelor's degree in life sciences or related field; certifications like CQE are commonHigh school diploma or associate degree; technical certifications may be preferred
Work EnvironmentLaboratories, manufacturing facilities, quality assurance departmentsManufacturing sites, laboratories, production lines
Job ResponsibilitiesData analysis, documentation, reviewing quality processes, supporting auditsPerforming tests, inspecting products, recording test results

While both roles support quality assurance, the Associate Quality Control Analyst typically focuses on data analysis and documentation, whereas the Quality Control Technician primarily conducts tests and inspections. The analyst role often requires a higher level of education and analytical skills, making it suitable for those interested in quality systems and compliance.

What does an associate quality control analyst do?

An Associate Quality Control Analyst is responsible for testing and inspecting products, materials, or processes to ensure they meet established quality standards. They perform routine laboratory tests, document results, and identify any deviations from specifications. These analysts often work in industries like pharmaceuticals, manufacturing, or food production, supporting senior analysts and quality managers. Their role is crucial in maintaining product safety, consistency, and regulatory compliance.

What are the key skills and qualifications needed to thrive as an associate quality control analyst?

To thrive as an Associate Quality Control Analyst, you need a solid background in biology, chemistry, or a related scientific field, often with a relevant bachelor's degree. Familiarity with laboratory equipment, quality management systems (such as LIMS), and regulatory guidelines like GMP is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying and resolving quality issues. These skills and qualifications ensure accuracy, compliance, and consistent product quality in laboratory and manufacturing environments.

Quality Control Associate

Zoetis, Inc.

Charles City, IA • On-site

Full-time

Posted 20 days ago


Zoetis rating

7.6

Company rating: 7.6 out of 10

Based on 77 frontline employees who took The Breakroom Quiz

59th of 86 rated pharmaceutical


Job description

States considered:
Role Description
Position Summary:
The Quality Control Associates role will work in collaboration with the other associates to ensure coverage of the following responsibilities; check in of test samples from manufacturing to the QC Scientists, prepare samples for shipment, completes filing of testing documentation, and organize and distribute samples for each testing group. This role also prepares samples for USDA submission, monitors the BMS alarms, and scans and archives test records. In addition, this role prepares Annual Product Reviews, completes Bio Expiry, and prepares documents for regulatory agencies and supports 20-08 preparation for submission to the USDA for final product release.
Position Responsibilities:
  • Distribute samples to applicable areas for testing
  • Maintain testing documentation, and ensure on time submission of documentation including 20-08s and samples to the USDA for final product release
  • Maintain appropriate departmental cGMP documentation.
  • File, scan, and archive of testing documentation
  • Support the Quality Control labs by completing basic skill testing.
  • Prepare Annual Product review for all products
  • Prepare 20-08 documentation for USDA submission
  • Responsible for Bio-Expiry completion
  • Responsible for 20/20 sample destroyals.
  • Visual inspection if products
  • Generation of Certificates of Approval (COA) for regulatory agencies
  • Revise specifications as necessary
  • Follow all Zoetis Quality Standards, Policies and Procedures
  • Seasoned individual contributor, fully proficient in role.
  • Performs complex tasks
  • Fully proficient in role, applies skills to complete a broad range of tasks.
  • Limited supervision with latitude for independent judgement.
  • Regularly completes assignments with little or no assistance.
  • Typically requires at least 3+ years of related experience.

Education and Experience:
  • High school education or GED required.
  • Post High School education in the Sciences, Business, or other related disciplines preferred.
  • 3-5years related experience in a manufacturing environment and / or QC Coordinator I level

Technical Skills Requirements:
  • Good mathematical, science and computer skills.
  • Demonstrated teamwork and collaboration skills required.
  • Strong communication skills required.
  • Comprehensive LIMS knowledge and experience
  • Understanding of 20-08 template requirements
  • Authorized Firm Sampler

Physical Requirements:
  • Must be able to walk, sit, or stand for long periods of time.
  • Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.
  • Must be able to work scheduled 40 hours with the ability to work overtime as needed.
  • Frequent lifting and carrying of 5 to 25 lbs.
  • Regular reaching, bending, stooping, and twisting.
  • Repetitive motion and substantial movement of the wrists, hands, and/or fingers.

Full time
Regular
Colleague
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn, including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from @zoetis.com, please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

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