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Day Shift Upstream Manufacturing Associate Jobs in Reston, VA

DC Logistics Associate - Day Shift

Reston, VA ยท On-site

$19 - $25.75/hr

Day Shift, Monday - Friday, 8:00am - 5:00pm We believe providing superior support and solutions for ... As the Data Center Logistics Associate position offers an opportunity to play a critical role in ...

DC Logistics Associate - Day Shift

Reston, VA ยท On-site

$19 - $25.75/hr

Day Shift, Monday - Friday, 8:00am - 5:00pm We believe providing superior support and solutions for ... As the Data Center Logistics Associate position offers an opportunity to play a critical role in ...

DC Logistics Associate - Day Shift

Reston, VA ยท On-site

$19 - $25.75/hr

Day Shift, Monday - Friday, 8:00am - 5:00pm We believe providing superior support and solutions for ... As the Data Center Logistics Associate position offers an opportunity to play a critical role in ...

Patient Care Coordinator

Manassas, VA ยท On-site

$17.50 - $23/hr

Prince William Family Medicine/ Integrity Rehab Group, a brand partner of Upstream Rehabilitation ... A day in the life of a Patient Care Coordinator: * Greets everyone who enters the clinic in a ...

Clinical Technician II, Day Shift

Arlington, VA ยท On-site

$19.17 - $29.90/hr

Position Title Clinical Technician II, Day Shift Purpose & Scope: The Clinical Technician II works ... The unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance is ...

Clinical Technician II, Day Shift

Arlington, VA

$21.75 - $28.25/hr

Position TitleClinical Technician II, Day Shift Purpose & Scope: The Clinical Technician II works ... The unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance is ...

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Day Shift Upstream Manufacturing Associate information

See Reston, VA salary details

$12

$21

$34

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

As of Jul 14, 2026, the average hourly pay for day shift upstream manufacturing associate in Reston, VA is $21.68, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $24.28 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, and why are they important?

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 job categories do people searching Day Shift Upstream Manufacturing Associate jobs in Reston, VA look for? The top searched job categories for Day Shift Upstream Manufacturing Associate jobs in Reston, VA are:
What cities near Reston, VA are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities near Reston, VA with the most Day Shift Upstream Manufacturing Associate job openings:
GMP Manufacturing Associate

GMP Manufacturing Associate

Planet Pharma

Rockville, MD โ€ข On-site

Other

Posted 12 days ago


Job description

Core hours M - F 8:30 am to 5 pm with flexible hours/shifts needed. Temp to possible perm.

Virtual Interview

The Downstream GMP Manufacturing Associate will work as part of a team and work directly in activities associated with purification that applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. The activities will take place in a cleanroom following aseptic techniques and procedures in a cGMP environment.


Duties and Responsibilities

Train on and perform Downstream purification activities such as Chromatography, Tangential flow filtration (TFF), Ultracentrifugation, and Final Formulation steps

Work in cleanroom environment while adhering to Standard Operating Procedures (SOPs) and Batch production Records (BPRs)

Prepare, sanitize, and disinfect equipment to prevent microbial contamination? Monitor processes using automated production systems and controls with supervision

Obtain and perform in-process sampling

Prepare buffers and solutions needed for Downstream activities, including at large scale (? 20L)

Perform various filter integrity tests throughout the process

Document all activities in Batch Records, Logbooks, Forms, etc.

Follow verbal and written procedures in operating production equipment and performing processing steps; accurately complete appropriate production documentation

Effectively communicate and interface with team to ensure the completion of daily activities

Operate manual and semi-automated equipment in support of routine production with minimal supervision

Edit and review Production Batch Records and Standard Operating Procedures Work in cleanroom environment while adhering to Standard Operating Procedures (SOPs)

Interact with other departments to complete activities associated with Downstream operations

Perform other tasks as assigned to support GMP Manufacturing that ensures sustainable right-first-time performance


Preferred Qualifications for the role

High School Diploma or Associate Degree with 0-2 years of experience in Downstream biologic production processes in a GMP environment in a Life Sciences Company; or Bachelor of Science in science or Engineering and 0-1 years of experience in Downstream biologic production processes in a GMP environment in a Life Sciences Company


Basic knowledge and understanding of purification processes

Ability to obtain sufficient hands-on experience with chromatography systems (AKTA systems at different scales) and approaches (Affinity, IEX, MMC), TFF modalities, and single use mixing systems

Ability to learn to operate manual and semi-automated equipment in support of routine production with supervision

Experience in the preparation of buffers

Experience editing and reviewing Production Batch Records and Standard Operating Procedures preferred

Organizational and planning skills

Ability to work in a Team and collaborative environment

Attention to detail and time management

Previous work in viral or vaccine production highly desired

Previous experience working for a Contract Manufacturing Organization (CMO) highly desired

Strong communication skills (writing, speaking, comprehending) highly desired

Basic computer skills including Microsoft (Word, Excel, Teams etc.)

Ability to work in a fast-paced environment's


Key Competencies

Demonstrates integrity and respect

Delivers results

Demonstrates business acumen

Fosters collaboration and teamwork

Champions change


Working Conditions

Operations are 24 hours per day, 7 days per week, and shift work will be required? Must be able to gown and pass gowning qualification to work inside a cleanroom for at least 4 consecutive hours

Must be able to work flexible hours must be willing to work outside of normally-scheduled hours as necessary

Must have reliable transportation to travel between sites in Rockville area Standing, (sometimes prolong standing), sitting, pushing, pulling, walking, bending, stooping, kneeling, and must be able to lift up to 50 lbs.