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Day Shift Upstream Manufacturing Associate Jobs in Silver Spring, MD

Buckeye Global IT Inc

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Biomanufacturing Associate ll (Upstream)

Rockville, MD · On-site

$25.50 - $28.50/hr

Follow instructions when performing planned manufacturing activities, in alignment with the batch ... day. Company Description Buckeye Global IT Inc, one of the fastest-growing IT and Healthcare ...

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Home Chef

Warehouse Associate - Day Shift

Baltimore, MD · On-site

$16 - $19/hr

This role follows a Day shift schedule, working from 7:00 AM to 5:30 PM, with designated days off on Wednesday, Thursday, & Friday. Warehouse associates will ensure the needs of both production and ...

Home Chef

Warehouse Associate - Day Shift

Baltimore, MD · On-site

$16 - $19/hr

This role follows a Day shift schedule, working from 7:00 AM to 5:30 PM, with designated days off on Wednesday, Thursday, & Friday. Warehouse associates will ensure the needs of both production and ...

J.J. McDonnell & Co

Warehouse Associate Day Shift

Elkridge, MD · On-site

$15.75 - $18.75/hr

Warehouse Associate This position is responsible for effectively and efficiently carrying out all ... As directed - performs daily end of shift inspections for cleanliness and to ensure that product ...

R E Michel CO

Warehouse Associate- Day Shift

Glen Burnie, MD · On-site

$15.75 - $18.75/hr

Ability to begin work at the start of the designated shift. Ability to work flexible hour schedule ... From our local branch associates and field sales people to our corporate support staff, they ...

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Day Shift Upstream Manufacturing Associate information

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How much do day shift upstream manufacturing associate jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for day shift upstream manufacturing associate in Silver Spring, MD is $21.54, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $24.09 per hour, depending on experience, location, and employer.

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.
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What cities near Silver Spring, MD are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities near Silver Spring, MD with the most Day Shift Upstream Manufacturing Associate job openings:
Day Shift Upstream Manufacturing Associate jobs near you

Associate Specialist (Cell Therapy Manufacturing)

AstraZeneca

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

21st of 86 rated pharmaceutical

Job description

Associate Specialist (Cell Therapy Manufacturing)
Introduction to role
Are you ready to bring precision and initiative to the start-up of a new cell therapy manufacturing facility-seeing your work translate into clinical trials that could change patients' lives? Join a team producing next-generation cell therapy products at a pivotal moment as our first clinical batches move from process development into cGMP operation.
In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes. You will help build the documentation, run sophisticated automated equipment in Grades A and B cleanrooms, and lead by example on the floor to keep every batch on track. Can you picture yourself owning a "right first time" mindset and guiding a shift handover that keeps a critical lot moving?
Accountabilities
  • GMP Documentation Excellence: Author and execute manufacturing batch records, work instructions, and SOPs with a "right first time" mindset; maintain bills of materials; reconcile batches promptly; document all activities to meet cGMP requirements; assist with deviations, non-conformances, and OOS investigations. Your rigor reduces errors, speeds release, and strengthens audit readiness.
  • Aseptic Equipment Operations: Monitor, clean, prepare, and operate automated cell processing, cell expansion, and filling equipment in Grades A and B cleanrooms. Your care and consistency protect product quality and patient safety.
  • Training and Knowledge Transfer: Train personnel on aseptic processing, equipment operation, cGMPs, documentation, and technical theory. By elevating team capability, you increase throughput and reliability.
  • Document Review and Continuous Improvement: Review batch records, SOPs, and logbooks for completeness, clarity, and accuracy; submit edits for revision as needed. Your attention to detail drives procedural clarity and repeatability.
  • Tech Transfer and Process Development: Participate in tech transfer activities; support development of platform processes; contribute to study and experiment designs; modify or improve processes and systems when appropriate. Your input helps mature processes from concept to cGMP readiness.
  • Floor Leadership and Problem Solving: Provide technical instruction; allocate administrative tasks; assign work to manufacturing staff; lead activities on the manufacturing floor; communicate product status at shift change; troubleshoot processing and equipment issues. Your leadership keeps operations aligned, responsive, and efficient.
  • Safety and Compliance Stewardship: Ensure a safe work environment in accordance with AstraZeneca standards. Your vigilance fosters a strong safety culture.
  • Flexibility: Weekend work may be required. Your adaptability ensures continuity of critical manufacturing runs.

Essential Skills/Experience
  • Bachelor's degree in life sciences, engineering, or a related field with 0-3 years of general cGMP manufacturing experience or a Master's degree in life sciences, engineering, or a related field with 0-2 years of general cGMP manufacturing experience
  • Basic knowledge in biologics manufacturing process, cell culture and/or vector products.
  • Technical proficiency in aseptic technique and working with manufacturing equipment in open and closed systems.
  • Working knowledge of automated manufacturing equipment and/or process analytical technologies.
  • Proficiency in Microsoft Word, Excel and data analysis.

Desirable Skills/Experience
  • Previous manufacturing or process development experience with cell therapy or vector products.
  • Dynamic individual with the ability to communicate and engage others.
  • Independent and self-starting. Ability to work with minimal supervision.
  • Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.

Why AstraZeneca
Here, your work sits close to the decision point and the patient impact. You will operate at the forefront of science with high visibility, shaping end deliverables across therapy areas and collaborating with unexpected teams in the same room to unleash bold thinking. We balance ambition with support-leaders empower you to improve, experiments are celebrated for what they teach, and resilient minds find inventive paths through a heavily regulated environment. You will expand your skills as you apply advanced technologies to complex problems, contribute to enterprise-recognized work, and bring courage and curiosity to challenges that truly matter. We value kindness alongside ambition, and we back people who speak up, share opinions, and turn critique into better solutions.
Step into this high-exposure manufacturing role and help deliver transformative cell therapies to patients-take the next step today and show us how your precision and initiative will raise our standards!
The annual base pay for this position ranges from $65,082 to $97,622. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
03-Aug-2026
Closing Date
04-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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