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Upstream Processing Manufacturing Associate

Upstream Processing Manufacturing Associate / Scientist

To support our next growth phase, we are hiring seven Upstream Manufacturing Scientists/Associates at various experience levels to meet the increasing demands of our Upstream and Downstream Manufacturing teams. These teams are gearing up to scale from pilot manufacturing to full-scale commercial production at our new NJ facility.

Positions Available:

  • Manufacturing Scientist I - III - from 1 years of experience +

USP Manufacturing Scientists:

  • Execute mammalian cell culture processes to produce recombinant proteins for biologics, managing cell culture batches up to 2000L.
  • Operate bioreactors, establish equipment specifications, and enhance manufacturing techniques.
  • Collaborate with manufacturing associates and engineers, providing clear instructions and guidance.
  • Initiate batch records, protocols, and oversee investigations in a cGMP environment to ensure compliance.
  • Review and document manufacturing and packaging batch records, ensuring adherence to safety standards and GMP guidelines.

Experience/Qualifications:

Upstream:

  • At least 1-2 years of experience in cell culture and bioreactor operations, including GMP and aseptic manufacturing experience.
  • Proficiency with single-use manufacturing consumables (e.g., bags, tube sets, columns) and experience in scale-up manufacturing activities.

Average salary estimate

$80000 / YEARLY (est.)
min
max
$70000K
$90000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Upstream Processing Manufacturing Associate, Pharma Universe

Are you passionate about biomanufacturing and ready to take your career to the next level? Join us at our cutting-edge facility as an Upstream Processing Manufacturing Associate! We're looking for enthusiastic Manufacturing Scientists at various levels of experience to help us meet the increasing demand for our Upstream and Downstream Manufacturing teams. As a key player in this exciting growth phase, you'll be working on everything from executing mammalian cell culture processes that produce essential recombinant proteins to managing large-scale bioreactor operations. Your role will involve hands-on work with bioreactors, establishing equipment specifications, and collaborating closely with our talented engineers and manufacturing associates. Together, you'll enhance our manufacturing techniques and ensure compliance in a cGMP environment. We value detail-oriented team players who can initiate batch records, oversee investigations, and ensure all manufacturing and packaging activities adhere to stringent safety standards. If you have a strong foundation in cell culture and bioreactor operations, along with a keen understanding of GMP and aseptic manufacturing practices, this position at our NJ facility could be the perfect match for your skills. Come and be a part of our vision to transition from pilot manufacturing to full-scale production, and help us shape the future of biologics production!

Frequently Asked Questions (FAQs) for Upstream Processing Manufacturing Associate Role at Pharma Universe
What responsibilities does the Upstream Processing Manufacturing Associate have at our company?

As an Upstream Processing Manufacturing Associate, you'll execute mammalian cell culture processes and manage bioreactor operations to produce recombinant proteins. Collaborating with both manufacturing associates and engineers, you'll provide guidance, initiate essential batch records, and ensure compliance with cGMP standards, playing a vital role in our manufacturing process.

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What qualifications are needed for an Upstream Processing Manufacturing Associate?

To be considered for the Upstream Processing Manufacturing Associate position, candidates typically need at least 1-2 years of experience in cell culture and bioreactor operations, along with proficiency in GMP practices and familiarity with single-use manufacturing consumables. A strong background in aseptic manufacturing is also essential for ensuring compliance and safety.

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What is the work environment like for an Upstream Processing Manufacturing Associate?

The Upstream Processing Manufacturing Associate operates in a state-of-the-art facility that emphasizes collaboration and innovation. Working in a cGMP environment, associates are involved in both routine processes and dynamic challenges that arise in scaling manufacturing from pilot to full production, making teamwork and communication key aspects of the role.

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How does the role of Upstream Processing Manufacturing Associate contribute to the company's growth?

The Upstream Processing Manufacturing Associate plays a critical role in our growth by helping to bridge the gap between pilot manufacturing and commercial production. By enhancing manufacturing techniques and ensuring efficient workflows, associates directly impact the scalability and quality of our biologic products, making their contributions invaluable.

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Is prior experience in biomanufacturing necessary for the Upstream Processing Manufacturing Associate role?

Yes, prior experience in biomanufacturing, specifically in cell culture and bioreactor operations, is vital for the Upstream Processing Manufacturing Associate role. Candidates with at least 1-2 years in GMP environments will find their experience highly relevant and beneficial as they contribute to our team's growing demands.

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Common Interview Questions for Upstream Processing Manufacturing Associate
Can you explain your experience with mammalian cell culture processes?

When responding to this question, highlight specific experiences, such as types of cell lines you have worked with and the scale of production. Detail any challenges you faced and how you overcame them, emphasizing your understanding of the processes involved.

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What steps do you take to ensure compliance with GMP standards?

Describe your familiarity with GMP practices, including how you document processes, maintain clean work environments, and ensure all procedures are followed meticulously. Providing examples of past experiences where you upheld GMP standards can strengthen your answer.

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How do you handle equipment troubleshooting in bioreactor operations?

Focus on your problem-solving skills and provide examples of past experiences where you identified equipment issues and successfully implemented solutions. Discuss the importance of collaborating with engineers and using your training to tackle challenges effectively.

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What are your strategies for managing batch records and documentation?

Elaborate on your attention to detail and organizational skills. Explain how you keep batch records accurate and up-to-date, highlighting any software or systems you are familiar with that assist in maintaining documentation integrity.

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Describe a successful collaboration experience with engineering teams.

Provide specific examples of projects where you worked closely with engineering teams. Discuss how you communicated effectively, shared knowledge, and contributed to successful outcomes, illustrating the importance of cross-team collaboration.

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What do you consider the most challenging aspect of upstream processing?

Your answer could discuss the variability of biological systems and how these can impact production. Mention any specific experiences where you adapted to these challenges to maintain quality and yield, showcasing your resilience and adaptability.

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How do you prioritize your tasks in a fast-paced manufacturing environment?

Discuss your time management techniques and how you assess task urgency and importance. Provide examples of situations where prioritization led to successful outcomes while minimizing downtime and ensuring compliance.

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What motivates you to excel in the field of biomanufacturing?

Sharing your passion for innovation, quality, and patient outcomes can resonate well. Talk about personal or professional experiences that drive your commitment to the field, showing your enthusiasm and dedication.

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How do you keep yourself updated with advancements in biomanufacturing technologies?

Mention how you actively seek out education, training, and professional development opportunities. This could include attending workshops, reading current literature, or participating in industry networks to stay on top of trends and advancements.

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What safety practices do you follow while working in a manufacturing lab?

Detail the safety protocols you adhere to, including proper use of PPE, lab protocols, and emergency procedures. Providing concrete examples where you communicated and enforced safety standards can strengthen your response.

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MATCH
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SENIORITY LEVEL REQUIREMENT
TEAM SIZE
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HQ LOCATION
No info
EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
April 7, 2025

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