1

Day Shift Upstream Manufacturing Associate Jobs in Nebraska

General Labor - Day Shift

Columbus, NE · On-site

$16.25 - $20.25/hr

Valmont impacts millions of people around the world every day, yet they might not realize the many ... We design, manufacture and coat. Our products and services make a difference. Join us, and BUILD ...

General Labor - Day Shift

Columbus, NE · On-site

$16.25 - $20.25/hr

Valmont impacts millions of people around the world every day, yet they might not realize the many ... We design, manufacture and coat. Our products and services make a difference. Join us, and BUILD ...

Manufacturing Operator (1st Shift)

Lincoln, NE

$15.25 - $18.25/hr

It unites us, inspires us, and challenges us to be better every day, driven by our agile ... About the role As a Manufacturing Operator you'll be part of the team that keeps our production ...

Showing results 21-40

Day Shift Upstream Manufacturing Associate information

What is a day shift upstream manufacturing associate?

A Day Shift Upstream Manufacturing Associate is responsible for preparing and operating equipment to support the initial stages of biopharmaceutical production, typically involving cell culture, fermentation, and media preparation. Working during the day shift, they monitor processes, maintain sterile environments, and ensure production runs smoothly and efficiently. Their work is crucial in ensuring quality and consistency in the early phases of manufacturing biological products such as vaccines or therapeutic proteins.

What is the difference between Day Shift Upstream Manufacturing Associate vs Night Shift Upstream Manufacturing Associate?

AspectDay Shift Upstream Manufacturing AssociateNight Shift Upstream Manufacturing Associate
Work HoursTypically 8 AM - 4 PMTypically 8 PM - 4 AM
Work EnvironmentManufacturing floor during daytime operationsManufacturing floor during nighttime operations
Required SkillsSimilar technical skills, safety protocols, and certificationsSame technical skills, safety protocols, and certifications
Employer UsageCommonly used in biopharma and biotech manufacturingSame industry usage, different shift timing

The main difference between a Day Shift Upstream Manufacturing Associate and a Night Shift Upstream Manufacturing Associate lies in their working hours. Both roles require similar skills, certifications, and work environments, but they operate during different shifts. Employers in biopharma and biotech industries often employ both to ensure continuous production, with shift timing being the primary distinction.

What are the typical collaboration points between a day shift upstream manufacturing associate and other teams in a biomanufacturing facility?

Day Shift Upstream Manufacturing Associates frequently collaborate with downstream processing teams, quality control, and process engineering staff. Daily responsibilities often involve communicating batch progress, troubleshooting issues, and ensuring compliance with safety and GMP standards. Clear documentation and timely reporting to supervisors and quality teams are crucial for maintaining production flow. This cross-functional teamwork ensures efficient handoffs and rapid response to any process deviations, making collaboration a key part of the role.

What are the key skills and qualifications needed to thrive as a day shift upstream manufacturing associate?

To excel as a Day Shift Upstream Manufacturing Associate, you typically need a background in biotechnology or life sciences, experience with aseptic techniques, and an understanding of Good Manufacturing Practices (GMP). Familiarity with bioreactors, cell culture systems, and process control software is commonly required, along with relevant safety or GMP certifications. Attention to detail, teamwork, and strong problem-solving abilities are valuable soft skills in this role. These competencies ensure the efficient and compliant production of high-quality biopharmaceuticals in a regulated manufacturing environment.
What are popular job titles related to Day Shift Upstream Manufacturing Associate jobs in Nebraska? For Day Shift Upstream Manufacturing Associate jobs in Nebraska, the most frequently searched job titles are:
What job categories do people searching Day Shift Upstream Manufacturing Associate jobs in Nebraska look for? The top searched job categories for Day Shift Upstream Manufacturing Associate jobs in Nebraska are:
What cities in Nebraska are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities in Nebraska with the most Day Shift Upstream Manufacturing Associate job openings:

Manufacturing Laboratory Technician - mAbs 1st Shift 8-hours (Monday - Friday and Rotating Weekends)

Zoetis, Inc.

Lincoln, NE • On-site

$17.75 - $23.50/hr

Full-time

Medical, Retirement, PTO

Posted 6 days ago


Zoetis rating

7.7

Company rating: 7.7 out of 10

Based on 78 frontline employees who took The Breakroom Quiz

54th of 86 rated pharmaceutical


Job description

Role Description :
Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals.
At Zoetis in Lincoln, NE we manufacture high quality medicines for companion animals and livestock. Our plant has been recognized as one of Nebraska's 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 Manufacturing Technician in the mAbs Department works in a GMP manufacturing laboratory environment for monoclonal antibody (mAb) production, executing both upstream and downstream operations. The role performs hands-on work using aseptic technique and GMP practices while following approved SOPs and batch records.
Upstream responsibilities include aseptic technique, inoculation and seed train support, mammalian cell culture maintenance, feeding and sampling, monitoring, and documenting critical process parameters, and operating culture equipment (e.g., bioreactors and associated systems) as required. Downstream responsibilities include harvest activities and purification operations such as centrifugation, chromatography, ultrafiltration, and nanofiltration, along with equipment setup, cleaning, and changeovers.
The technician ensures compliance and product quality through accurate, timely documentation, adherence to safety protocols for biological materials, chemicals, and equipment.
Hours: 1st Shift, 7:15am - 3:45pm (8-hours) Monday - Friday and rotating weekends. Overtime and holidays may be required.
Position Responsibilities
Perform processes and operate equipment required for large-scale monoclonal antibody (mAb) production campaigns.
Employee Responsibilities:
-Support large-scale GMP biologics production campaigns by performing upstream and downstream manufacturing operations, including:
• Aseptic inoculation, expansion, and cultivation of mammalian cell cultures across multiple scales (e.g., seed train through production)
• Operation and monitoring of bioreactors, isolator gloveboxes, and associated automated manufacturing equipment.
• Execution of equipment cleaning-in-place (CIP) and steam-in-place (SIP) procedures in accordance with SOPs and batch records
• Perform chromatography, ultrafiltration (UF), and nanofiltration (NF), as required by the process.
• Inventory management for materials and consumables (receipt, staging, reconciliation), and sampling in support of in-process testing and release requirements.
-Perform routine equipment maintenance and troubleshoot issues as needed
-Accurately complete and maintain process documentation in compliance with GMP standards to ensure product quality
-Adhere to all safety policies and procedures related to biological and chemical handling, as well as equipment use
-Collaborate effectively with cross-functional teams and other departments to support production goals
Education and Experience
High school degree or equivalent is required. Bachelor's or master's degree preferred.
The ideal candidate would possess:
• BS in Biology, Chemistry, Biochemistry, Biotechnology, or a related field
• Previous experience in large-scale production or laboratory scale
• Excellent communication skills and attention to detail
• Ability to prioritize work, think critically, and take initiative.
• Ability to work well in a team environment as well as work independently with minimal supervision when needed.
Preference will be given to candidates with relevant experience in biological production, aseptic manufacturing, or in a regulated environment.
Technical Skills and Competencies Required
Functional skills:
• Ability to read and follow written directions.
• Ability to complete basic calculations.
• Ability to think critically.
Technical skills:
• Basic mechanical skills
• Ability to troubleshoot.
• Knowledge of the metric system
Desirable skills:
• Mammalian cell culture practices and techniques
• Fundamental understanding of bioreactors/fermenters or downstream purification techniques
• Basic understanding of biological and chemical principles
• Experience with Outlook, Excel, and Word
• Experience within a regulated environment.
Physical Position Requirements
Exposure to chemicals, fumes, odors, noise, live steam, temperature fluctuations, biohazards, continuous standing and lifting to a maximum of 50 lbs.
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.

What Zoetis employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom