What is it like to work for Zoetis, the world leader in animal health? Zoetis means something a little different to every colleague, but at our core, our purpose ‘to nurture the world and humankind by advancing care for …
Skills: Packaging Engineering, GMP Compliance, Process Validation, Root Cause Analysis, Project Management
What is it like to work for Zoetis, the world leader in animal health? Zoetis means something a little different to every colleague, but at our core, our purpose ‘to nurture the world and humankind by advancing care for …
Skills: Packaging Engineering, GMP Compliance, Process Validation, Root Cause Analysis, Statistical Evaluation
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The Process Engineer provides primary engineering support for packaging, visual inspection, and product transfers during facility startup and commissioning. They are responsible for optimizing packaging processes, developing user requirements for capital equipment, and ensuring GMP compliance.
Requirements
Requires a BS in Engineering with 6+ years of experience in a regulated manufacturing environment, preferably in aseptic packaging or medical devices. Proficiency in Operational Excellence tools and software such as PAS-X, SAP, or Minitab is highly desired.
Full job description
What is it like to work for Zoetis, the world leader in animal health? Zoetis means something a little different to every colleague, but at our core, our purpose ‘to nurture the world and humankind by advancing care for animals’ is what unites us in all our roles.
We are a global animal health company dedicated to serving veterinarians, livestock producers and people who raise and care for farm and companion animals in more than one hundred countries. And we are excited to become a part of the Lithia Springs, GA, community as we build our newest manufacturing facility to support our growing monoclonal antibody and vaccine portfolios.
We are currently searching for a Process Engineer to join our team.
POSITION SUMMARY
This position will be responsible for providing primary engineering support for all Packaging, visual inspection, and support Packaging line and product transfers. It will support Packaging startup and commissioning activities. This position will also support other areas of the facility as the business needs dictate. The ideal candidate will use GMP industry best practices and their expertise to measure, analyze and specify requirements that lead to best-in-class quality products and design for manufacturability. We are looking for a highly motivated candidate who can work cross-functionally in a highly regulated GMP compliant environment.
IMPACT AND ORGANIZATIONAL CONTRIBUTION
Act as Packaging system owner during start up activities
Lead and support Packaging implementation and improvements.
Support the implementation and use of PAS-X.
Support generation, review, and approval of Packaging SOPs.
Support deviations/change controls associated with Packaging line and product transfers.
Lead projects relating to the development and optimization of Packaging processes, including plant design, process equipment/workflows, and material handling.
Evaluate existing Packaging processes and for improvements in capacity, efficiency, and product quality in alignment with business needs.
Improve testing methods and quality control measures, incoming materials, standards, and controls.
Develop user requirements for new capital equipment, survey potential equipment suppliers, submit RFQs, evaluate proposals from suppliers, and provide recommendations for purchase.
Develop and execute test protocols and reports to validate new or modified processes.
Strong ability to investigate root causes of Packaging issues impacting product quality or yield, support implementation of improvements, countermeasures, and preventative action.
Identify sources of variation (procedure, process, equipment, people) within the Packaging process and design solutions.
Recognizes the need for and embraces the concept of continuous improvement. Creates innovative ideas and recommendations based on engineering data, facts, and observations.
Collects process data and performs trending and statistical evaluation to monitor process performance to understand stability and areas for improvement.
Effectively partners with and motivates enabling support teams to improve operations for the advancement of the entire site and company.
Maintain quality control and safety standards.
Actively contributes to meeting business objectives around compliance, cost savings, and potential capital spending requirements.
Assists in completing validation activities as required.
Assists in non-conformance and CAPA investigations.
Assist in training and development of team members.
EDUCATION AND EXPERIENCE
BS in an Engineering discipline with 6+ years of experience.
Food and Drug Administration, USDA, and/or work in a regulated manufacturing environment, preferably in aseptic manufacturing or Packaging, or medical device industry, is required.
Proven experience in the application of engineering principles to the design and improvement of manufacturing processes.
Experience working with GMP contract manufacturing organizations and third-party suppliers.
Experience with pharmaceutical equipment and test method validation is preferred.
Experience with Operational Excellence tools such as DMAIC, 5 WHY’s, Fishbones, FMEA, etc.
Green belt or Black belt certification is a plus.
Demonstrated ability to interact effectively with colleagues and management across departmental boundaries.
Candidates must possess flexibility and agility to respond to constantly changing conditions and priorities.
Proficient computer skills such as PAS-X or electronics batch record (EBR/MES), Excel, Word, MS Visio, JMP, Minitab, SAP, or similar software
Must be willing to quickly learn and become proficient in common systems used to manage the business – to include production schedule, quality deviations, ERP system, and change control.
Work Environment: Colleague must work onsite, be able to lift at least 50 pounds, and work near moving mechanical parts with moderate noise level where the use of hearing protection is optional, and eye protection is required.
This position is eligible for short-term incentive compensation.
We offer a competitive and comprehensive benefits package, which includes healthcare, dental coverage, and retirement savings benefits along with paid holidays, vacation, and disability insurance.
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 [email protected] 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.
Nurturing our world and humankind by advancing care for animals
Industry
Pharmaceutical Manufacturing
Company size
10,001+ employees
Founded
2013
Headquarters
Parsippany, NJ
LinkedIn followers
630,120
Total funding
$3.6B
The world’s leading animal health company. We’ve been pioneering ways to predict, prevent, detect, and treat animal illness for over 75 years, supporting veterinarians, livestock producers, and pet owners in over 100 countries. We integrate science, R&D, manufacturing and commercial excellence to deliver innovation across animal health solutions.
Community Guidelines:
This page is intended to share how Zoetis is advancing care for animals. We aspire to create a supportive community, but there are guidelines to which posts and comments on this page must adhere.
If your post references a side effect related to any Zoetis product, we may contact you for more information. To monitor the safety of Zoetis products, we advise you to call our Veterinary Medical Information and Product Support Team at 1-888-963-8471; Support Team is available Mon-Fri 9am to 6:30pm ET.
We reserve the right to remove any post/comment that violates LinkedIn Guidelines. Please refrain from posting comments that include:
Medical advice
Vulgarity/profanity/obscene content
Discriminatory/derogatory comments/hate speech
Disinformation
Politics/religion
Personal attacks/ harassment/threats
Promotion of illegal activity
Copyright/trademark infringements
Advertising/self-promotion
Graphic/disturbing imagery
Images/flyers/links/videos with no context/commentary
Spam (repeatedly posting same/similar comments)
Repeated or severe violations may result in content removal and/or the user being muted, removed, or blocked.
Our regular business hours are Mon-Fri 9am to 5pm ET. Zoetis does not endorse and is not responsible for information and opinions shared by community members. The information shared is provided for educational purposes only and is not intended to replace discussions with an animal healthcare professional. Testimonials represent individual experience only and the experiences and opinions of community members may be unique to the speaker. Terms of Use: https://www.zoetis.com/terms-of-use
Offices: 10 Sylvan Way, Parsippany, NJ 07054, US · Mercuriusstraat 20, Zaventem, Flemish Region 1930, BE
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