Zoetis
Job Opportunity at Zoetis
Zoetis is the world's largest manufacturer and supplier of animal pharmaceuticals. Our plant in Lincoln, NE, has been recognized as one of Nebraska's safest companies, with a long-standing presence in the community. We are a clean, modern site that continues to innovate and grow. Position Summary Perform tasks necessary to ensure control of GMP documents utilized for Biological, Pharmaceutical, and Veterinary Medicine Research & Development operations according to current policies and procedures. Hours: 1st Shift, 7:30am
4:00pm. Occasional overtime may be required. Position Responsibilities Prioritize workload on a daily basis to respond to the changing manufacturing schedule. Maintain a safe work environment and participate in site safety program initiatives. Work with manufacturing and VMRD to update batch records and other manufacturing GMP documents according to site change control procedures. Maintain central documentation databases. File and archive GMP records using central documentation systems according to SOP and Zoetis record retention policy. As needed, assist with retrieving GMP records during inspections (i.e., batch records, protocols, etc.) Manage issuance and archival of notebooks and logbooks. Assist with other group activities as requested, including use/support of quality systems (Veeva Vault, ETS, LMS, and SAP), support of annual product review, risk assessments, change control, stability program, and regulatory inspections. Perform other duties and special projects, as assigned. Education and Experience Associate degree or equivalent post high school education or equivalent experience 1-2 years relevant work experience preferred. Technical Skills and Competencies Required Advanced proficiency in Word and Excel Microsoft applications Strong time management skills with proven experience in multi-tasking and prioritization Process and detail oriented with the ability to follow complex processes and prepare detailed structured documents. Demonstrated organizational and administrative skills and the ability to communicate effectively with multiple organizations. Ability to work within a team and independently. Preferred Candidate Qualifications Working knowledge of US-FDA, EU, and international registration requirements Experience in change management processes, manufacturing operations, quality operations, and/or regulatory affairs. Experience with training documentation systems, quality tracking systems, laboratory information management systems, and manufacturing planning systems. Experience in access, SharePoint, Microsoft Teams & SAP applications. Physical Position Requirements This position requires sitting, standing, lifting, and walking with occasional overtime. 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 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.
Zoetis is the world's largest manufacturer and supplier of animal pharmaceuticals. Our plant in Lincoln, NE, has been recognized as one of Nebraska's safest companies, with a long-standing presence in the community. We are a clean, modern site that continues to innovate and grow. Position Summary Perform tasks necessary to ensure control of GMP documents utilized for Biological, Pharmaceutical, and Veterinary Medicine Research & Development operations according to current policies and procedures. Hours: 1st Shift, 7:30am
4:00pm. Occasional overtime may be required. Position Responsibilities Prioritize workload on a daily basis to respond to the changing manufacturing schedule. Maintain a safe work environment and participate in site safety program initiatives. Work with manufacturing and VMRD to update batch records and other manufacturing GMP documents according to site change control procedures. Maintain central documentation databases. File and archive GMP records using central documentation systems according to SOP and Zoetis record retention policy. As needed, assist with retrieving GMP records during inspections (i.e., batch records, protocols, etc.) Manage issuance and archival of notebooks and logbooks. Assist with other group activities as requested, including use/support of quality systems (Veeva Vault, ETS, LMS, and SAP), support of annual product review, risk assessments, change control, stability program, and regulatory inspections. Perform other duties and special projects, as assigned. Education and Experience Associate degree or equivalent post high school education or equivalent experience 1-2 years relevant work experience preferred. Technical Skills and Competencies Required Advanced proficiency in Word and Excel Microsoft applications Strong time management skills with proven experience in multi-tasking and prioritization Process and detail oriented with the ability to follow complex processes and prepare detailed structured documents. Demonstrated organizational and administrative skills and the ability to communicate effectively with multiple organizations. Ability to work within a team and independently. Preferred Candidate Qualifications Working knowledge of US-FDA, EU, and international registration requirements Experience in change management processes, manufacturing operations, quality operations, and/or regulatory affairs. Experience with training documentation systems, quality tracking systems, laboratory information management systems, and manufacturing planning systems. Experience in access, SharePoint, Microsoft Teams & SAP applications. Physical Position Requirements This position requires sitting, standing, lifting, and walking with occasional overtime. 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 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.