drjobs Test Record Specialist – Quality Operations Microbiology Laboratory 1st Shift

Test Record Specialist – Quality Operations Microbiology Laboratory 1st Shift

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1 Vacancy
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Job Location drjobs

Lincoln, NE - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Zoetis is the worlds largest Manufacturer and Supplier of Animal Pharmaceuticals.

At Zoetis in Lincoln NE we manufacture high quality medicines for dogs cats and livestock. Our plant has been recognized as one of the Nebraskas Safest Companies with a long-standing presence in the Lincoln community. We are a clean modern site that continues to innovate and grow.

Benefits Include:

$500 Sign on Bonus

4 weeks accrued paid vacation and 13 paid holidays.

401(k) match with company profit sharing.

Tuition reimbursement and Student Loan repayment program.

Great Health personal and family benefits starting day 1.

Position Summary

The MCL Test Record Specialist plays a key role in ensuring the accuracy and compliance of laboratory test records that support product release. Under close supervision this position is responsible for reviewing identifying corrections and approving routine test records and results in accordance with current Good Manufacturing Practices (cGMP) Standard Operating Procedures (SOPs) and regulatory requirements (e.g. FDA USDA EU). The specialist also supports documentation management assists in laboratory investigations contributes to continuous improvement efforts and ensures safe work practices. Effective communication across departments and attention to detail are essential for success in this role.

Hours:1st shift. Overtime weekend and holiday work may be required.

Position Responsibilities

Under close supervision the MCL Test Record Specialist reviews identifies any corrections and approves routine test records and results in compliance with all relevant SOPs and testing procedures to support product release.

  • Ensure compliance with cGMP SOPs and regulatory requirements (e.g. FDA USDA EU).
  • Review reconcile and approve laboratory test records and documentation for accuracy and completeness.
  • Compile verify and report test results using Laboratory Information Management Systems (LIMS).
  • Scan upload and transfer test records and documents between labs and documentation areas.
  • Support updates to Testing SOPs and Master Control Documents (MCDs).
  • Assist in laboratory investigations and contribute to continuous improvement initiatives.
  • Identify and report quality or safety concerns to supervisory personnel.
  • Demonstrate safe work practices and recognize potential hazards.
  • Communicate effectively across departments and shifts.

Education and Experience

Required:

  • Two years associate degree in science or
  • One to two years relevant experience with relevant science-based college courses.

Preferred:

  • Bachelors degree in biological sciences/chemistry
  • Experience with cGMP documentation.
  • Competent using Window-based applications.

Technical Skills and Competencies Required

Required:

  • Basic understanding of microbiology techniques knowledge of cGMP documentation excellent organization verbal and written communication skills

Physical Position Requirements

  • Manual dexterity using hands and fingers.
  • Specific vision abilities required by this job include close vision work.
  • Occasional need to sit reach with hands and arms.
  • Ability to work flexible hours work weekend and overtime

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.

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 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 site or (2) via email to/from addresses using only the Zoetis domain of @. 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.

Required Experience:

Unclear Seniority

Employment Type

Full-Time

Company Industry

About Company

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