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Day Shift Upstream Manufacturing Associate Jobs in Silver Spring, MD

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Title: BMA Upstream BMA I Pay Rate $25.50 BMA II Pay Rate $28.50 Location: Rockville MD 20850 ... Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through ...

Clinical Technician, Day Shift

Arlington, VA · On-site

$22 - $28.25/hr

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

Clinical Technician, Day Shift

Arlington, VA · On-site

$19.17 - $29.90/hr

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

Clinical Technician, Day Shift

Arlington, VA

$21.75 - $28.25/hr

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

... shift differentials (where applicable), internal equity, and current market conditions. The posted ... The unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance is ...

Clinical Technician, Day Shift

Arlington, VA · On-site

$19.17 - $29.90/hr

... shift differentials (where applicable), internal equity, and current market conditions. The posted ... The unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance is ...

Showing results 21-40

Day Shift Upstream Manufacturing Associate information

See Silver Spring, MD salary details

$12

$21

$34

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

As of Aug 17, 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 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 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 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 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:

Biomanufacturing Associate

Azaaki Solutions

Rockville, MD • On-site

$31.50/hr

Contractor

Posted 5 days ago

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Job description

Title: BMA Upstream

BMA I Pay Rate $25.50

BMA II Pay Rate $28.50
Location: Rockville MD 20850

Duration: 4+Months

Description:

Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through Friday
OT and weekend work may become required
there is a possibility of extension or conversion at end of 6 months

Position Summary:

The Biomanufacturing Associate II plays an integral role within CRL’s gene therapy manufacturing function by applying biological, bioprocess, manufacturing, mechanical, application, system, and technology principles, processes, procedures, inputs, and outputs, for designated production processes and handovers within a regulated environment to ensure the timely production and release of quality products, based on client specifications.

Key Responsibilities and Duties:

  • Apply and adhere to SOPs, cGMP, GLP, Quality, and Safety requirements.
  • Effectively execute a range of tasks, in line with SOPs, in the following area:
    • Upstream Activities (e.g., solutions, media aliquot, and buffer preparation and autoclave materials for cell culture, staging of raw materials, seed train, bioreactor set up, fermentation monitoring and/or harvest).
  • Follow instructions when performing planned manufacturing activities, in alignment with the batch record.
  • Prepare, edit, and complete quality documents. Well-versed in applying GDP.
  • Ensure data integrity - accurately document and review work prior to submission.
  • Document, record, investigate, and report observed process variances/deviations, in real time.
  • Follow instructions when operating equipment. Prepare, clean, and maintain equipment/tools.

Title: BMA Downstream

Location: Rockville MD 20850

Duration: 4+Months

Pay Rate $31.50/hr.

Qualifications:

  • HS Diploma/equivalent and 6 years of related experience, A.S. with 5 years, or a B.S. in biology/life sciences, bioengineering, or related discipline with 3 years of related experience.
  • Prior cell/gene therapy experience in a highly technical role, covering a wide range of tasks, within a cGMP/biotech manufacturing environment or related industry/role.
  • Informal coaching or project management experience is desirable.
  • Qualified as a LEAN trainer or willing to become qualified.

 Pay Rate $23.5/hr.

Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through Friday
OT and weekend work may become required
there is a possibility of extension or conversion at end of 6 months

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