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Biotech Manufacturing Associate Jobs in Delaware

Lab Tech - I (Associate)

Millsboro, DE · On-site

$41K - $46K/yr

Responsibilities Join a Manufacturing Operations team responsible for producing high-quality biotechnology products in a regulated manufacturing environment. Team members work with a Safety First ...

... Biotech Campus will play a pivotal role in the manufacture of our company's biologics-based medicines, including the areas of immuno-oncology. This site will establish our company's internal ...

Warehouse Associate

Middletown, DE · On-site

$15 - $18/hr

Collaborate with QA, QC, Manufacturing, MSAT/Engineering, Planning/Procurement, and EHS. Equipment ... pharma/biotech, medical device, food, or other regulated industry preferred. (GMP) * Experience ...

Biotech Manufacturing Associate information

See Delaware salary details

$12

$20

$33

How much do biotech manufacturing associate jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for biotech manufacturing associate in Delaware is $20.86, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

What are Biotech Manufacturing Associates?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What jobs can I get with an associate's degree in biotechnology?

Biotech Manufacturing Associates are common roles for those with an associate's degree in biotechnology, involving tasks such as preparing and operating laboratory equipment, following strict safety protocols, and documenting processes. Other positions include quality control technician, laboratory technician, and production operator, often requiring knowledge of GMP standards and familiarity with lab tools and procedures.

What does a biotech associate do?

A biotech manufacturing associate is responsible for performing tasks related to the production of biotechnological products, such as preparing equipment, following manufacturing protocols, and ensuring quality control. They often work in laboratory or cleanroom environments, using tools like bioreactors and adhering to safety and regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing, processing, and packaging biological products in a manufacturing environment. They operate equipment, follow strict safety and quality protocols, and document production activities to ensure compliance with regulatory standards. The role often requires attention to detail, knowledge of GMP practices, and the ability to work in a team setting.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by Biotech Manufacturing Associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

How much does a manufacturing associate make at KBI Biopharma?

A Biotech Manufacturing Associate at KBI Biopharma typically earns between $50,000 and $70,000 annually, depending on experience and location. The role involves working in a regulated environment, often requiring knowledge of GMP protocols and bioprocessing equipment.

What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.
What are popular job titles related to Biotech Manufacturing Associate jobs in Delaware? For Biotech Manufacturing Associate jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Biotech Manufacturing Associate jobs in Delaware look for? The top searched job categories for Biotech Manufacturing Associate jobs in Delaware are:
What cities in Delaware are hiring for Biotech Manufacturing Associate jobs? Cities in Delaware with the most Biotech Manufacturing Associate job openings:
Infographic showing various Biotech Manufacturing Associate job openings in Delaware as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $43,379 per year, or $20.9 per hour.
Downstream Operations Scientist

Other

Re-posted 12 days ago


University Of Delaware rating

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Company rating: 5.7 out of 10

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Job description

Downstream Operations Scientist

Apply now Job no: 502528
College / VP Area: Research Office
Work type: Staff
Location: Newark, DE
Categories: Research & Laboratory, Full Time

Curious about the full value of working at UD? In addition to salary, our Total Rewards benefits and Compensation Estimator give you a clear view of the complete package.

Pay Grade: 33E

Context of the Job:

The Downstream Operations Scientist is responsible for leading downstream purification unit operations for materials from bioreactors and shake flasks with culture volumes ranging from 250mL to 50L in scale at the National Institute for Innovation in Manufacturing Biopharmaceuticals (NIIMBL). The work will involve 21CFR58 compliant downstream operations and data analysis, including utilizing automation systems. The scientist will also collaborate with bioreactor specialists and an analytical team.

Among other activities, NIIMBL executes technical projects that advance the readiness levels of relevant technologies, assays, and methods. The scopes of scientific projects generally include many organizations as partners and collaborators such as scientists from several large and small companies, a scientist from a Federal agency, and a scientist from a University. Many of these projects will be hosted at the University of Delaware in a state-of-the-art laboratory facility purpose-built for such studies. These projects will involve a diverse set of technologies and approaches and address drug substance, drug product, and analytical needs by the industry appropriate to several types of biopharmaceuticals: vaccines, therapeutic proteins and antibodies, antibody-drug conjugates, bispecific antibodies, gene therapy vectors, and cell therapies, among others.

Major Responsibilities

  • Serve as a lead technical scientist on multiple projects involving downstream purification unit operations for the manufacture of industrially relevant products and related activities.
  • Adhere to 21CFR58 GxP guidelines in execution of work.
  • Set-up, operate, troubleshoot, maintain, and clean downstream bioprocessing equipment.
  • Use manufacturing experience to identify process parameters and define their setpoints.
  • Perform DoE studies to confirm the impact of process parameters on impurity levels, product recovery, and potency.
  • Characterize performance of existing purification and formulation unit operations, including column chromatography (e.g., ProA, SEC, CEX, AEX), filtration, TFF, and bulk filling.
  • Develop new primary recovery unit operations such as centrifugation, homogenization, flocculation, tangential-flow filtration (TFF), and depth filtration.
  • Develop new chromatography unit operations, from screening and characterization to optimization and initial scale-up.
  • Optimize buffer compositions to improve the stability and solubility of target molecules.
  • Collaborate with an analytical team to adapt and troubleshoot research analytical methods such as HPLC, SDS-PAGE, enzyme activity and endotoxin assays to quantify yield, activity, and purity at various stages of the manufacturing process.
  • Document all work and analyses in an electronic lab notebook. Perform tracking and trend analysis of method performance.
  • Analyze process performance trends, perform statistical data analysis, and present data to teams.
  • Partner with Informatics Infrastructure team on deploying structured data capture systems.
  • Draft and revise SOPs and batch records.
  • Maintain detailed documentation of lab activities and tabulation of data.
  • Compile data generated to present and discuss at team meetings.
  • Author, review and edit technical reports and manuscripts intended for publication.
  • Stay current with relevant technologies and scientific literature.
  • Perform other job-related duties as assigned.

Qualifications:

  • A Masters in chemical engineering or relevant life science discipline and 5 years of industrially relevant downstream purification experience is required with preference for experience in a 21CFR58-compliant GxP environment, or a PhD in chemical engineering or relevant life science discipline and 2 years of industrially relevant downstream purification experience is required with preference for experience in a 21CFR58-compliant GxP environment.
  • Hands-on experience with a range of downstream unit operations and control systems, experience with DeltaV preferred.
  • Operates chromatography skids and other bioprocess equipment for purification of industrially relevant materials.
  • Knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
  • Possess a contribution mindset fueled by an inner drive to take initiative without being directed.
  • Excellent interpersonal and managing skills with the desire to work collaboratively and effectively in a team environment.
  • Ability to demonstrate effective leadership through communication, respect, influence, persuasion, and trust.
  • Excellent problem solving and critical thinking skills.
  • Excellent writing, communication, and presentation skills.
  • Strong MS Excel, PowerPoint, and Word skills. Microsoft Project skills.
  • Excellent organization and planning skills.
  • Strong attention to detail and ability to adhere to standards procedures.
  • Ability to function in a rapidly changing environment.

Notice of Non-Discrimination and Equal Opportunity
The University of Delaware does not discriminate against any person on the basis of race, color, national origin, sex, gender identity or expression, sexual orientation, genetic information, marital status, disability, religion, age, veteran status or any other characteristic protected by applicable law in its employment, educational programs and activities, admissions policies, and scholarship and loan programs as required by Title IX of the Educational Amendments of 1972, the Americans with Disabilities Act of 1990, Section 504 of the Rehabilitation Act of 1973, Title VII of the Civil Rights Act of 1964, and other applicable statutes and University policies. The University of Delaware also prohibits unlawful harassment including sexual harassment and sexual violence.

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