Associate QA Specialist

Zoetis, Inc

Charles City (IA)

On-site

USD 65,000 - 90,000

Full time

6 days ago
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Job summary

Zoetis, Inc is seeking a Quality Assurance professional for a full-time role in Charles City, Iowa. You will collaborate with manufacturing colleagues to oversee investigations, perform batch-record reviews, and support regulatory inspections while ensuring compliance with GMP and internal policies.

The role requires strong CAPA and root cause analysis skills, proficiency with SAP and MS Office, and excellent English communication. Travel may be necessary as part of the QA activities.

Qualifications

  • BA/BS in a relevant field; 0–2 years for Associate or 2–4 years for Specialist.
  • CAPA, Analytical Problem Solving and Root Cause Analysis preferred; basic problem-solving skills.
  • Excellent verbal and written communication in English.
  • Proficient with SAP, Word, Excel, and PowerPoint.
  • Excellent organizational skills and ability to multitask.
  • Willingness to embrace change and adjust to priorities.
  • Travel may be required.

Responsibilities

  • Tracking documents to ensure timely review for release.
  • Review and approve SOPs to maintain compliance.
  • Perform batch record reviews.
  • Prepare for and participate in regulatory inspections (foreign and domestic).
  • Develop/revise and maintain QA SOPs.
  • Audit manufacturing processes for compliance with licenses.
  • Review documentation and collect site metrics data.
  • Support all QA areas and release-related items.
  • Review and approve deviations and related action items.

Skills

CAPA
Analytical problem solving
Root cause analysis
Verbal communication
Written communication
Team collaboration
Travel may be required

Education

BA/BS degree in a relevant field

Tools

SAP
Word
Excel
PowerPoint

Job description

Job Description:

Work with internal manufacturing colleagues as a cross functional member and approver of Zoetis investigations. Participates in production lab walk through audits prior/post construction projects as well as on-going maintenance activities requiring Quality oversite. Provides manufacturing floor support as needed to maintain compliance with local policies and procedures. Review and approval of Environmental monitoring data and reports. Participates in/ supports regulatory inspections as well as follow up action items. Perform batch record reviews and review of other records relating to processing of components, materials and finished veterinary biological for comparison with approved specifications and regulatory requirements.

Position Responsibilities:
  • Tracking of Documents to ensure timely review to complete release on time.
  • Review and approval of Standard operating procedures to maintain compliance.
  • Perform assigned batch record reviews.
  • Participate in the preparation for and execution of foreign and domestic regulatory agency inspections.
  • Develop/revise, implement and maintain assigned Quality Assurance standard operating procedures.
  • Audit manufacturing processes for compliance against approved regulatory licenses.
  • Documentation review.
  • Data collection for site Metrics.
  • Support roles for all areas of Quality.
  • Database review for support of release.
  • Actively support, review, and approve of all manufacturing/environmental/ GMP deviations as well as related items (action items, commitments tracking, etc) related to manufacture of veterinary biological products at the Charles City, Iowa facility.
  • Conduct walk through audits as part of the paint and patch process as well as ongoing construction activities being conducted at the site.
  • Performs product related system dispositions based on local site procedures.
  • Participates on in the Change Management process either as a team member or change agent.
  • Participate in the preparation for and execution of foreign and domestic regulatory agency inspections.
Education and Experience:
  • Associate: BA/BS with 0-2 years of experience OR Minimum of 6 years relevant experience. Specialist: BA/BS with 2-4 years of experience OR Minimum of 8 years relevant experience.
  • Training in CAPA, Analytical Problem Solving and Root Cause Analysis preferred. Basic problem-solving skills.
  • Excellent verbal and written communication skills, fluent in English.
  • Proficient with the following software programs: SAP, Word, Excel, and PowerPoint .
  • Excellent organizational skills and strong ability to multi-task.
  • Willingness to positively embrace change and flexibility in adjusting to changing priorities.
  • Strong attention to detail, ability to work well independently and as part of a team, and to work effectively with people at all levels within the organization.
  • Travel may be required.
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, 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.
  • t of the wrists, hands, and/or fingers.

Full timeRegularColleague

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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