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Biomanufacturing Associate Jobs in Ohio (NOW HIRING)

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate's degree in a technical discipline desirable * 2 Years experience with building fire ...

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate degree in Engineering, a related discipline, or equivalent trade school. * 5+ years of ...

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associate degree in Engineering, a related discipline, or equivalent trade school. * 5+ years of ...

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associates degree in engineering or a related discipline or equivalent mechanical trade school ...

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is ... Associates degree in engineering or a related discipline or equivalent mechanical trade school ...

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Biomanufacturing Associate information

See Ohio salary details

$25.7K

$134.2K

$295.2K

How much do biomanufacturing associate jobs pay per year?

As of Aug 12, 2026, the average yearly pay for biomanufacturing associate in Ohio is $134,247.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,900.00 and $202,000.00 per year, depending on experience, location, and employer.

What is a biomanufacturing associate?

A Biomanufacturing Associate is a professional who assists in the production of biopharmaceutical products, such as vaccines and therapeutic proteins, using biological systems like living cells. They are responsible for operating equipment, monitoring processes, following strict safety and quality protocols, and documenting production activities. Biomanufacturing Associates play a vital role in ensuring that products are made efficiently and meet regulatory standards in highly controlled environments.

What is the difference between Biomanufacturing Associate vs Quality Control Technician?

AspectBiomanufacturing AssociateQuality Control Technician
Required CredentialsAssociate degree in biology, chemistry, or related fieldAssociate degree or certification in quality control or laboratory techniques
Work EnvironmentManufacturing floor, production areasLaboratories, testing facilities
Employer & Industry UsageBiotech, pharmaceutical manufacturingPharmaceutical, biotech, and medical device companies

Biomanufacturing Associates focus on the production process, operating equipment, and ensuring manufacturing runs smoothly. Quality Control Technicians primarily perform testing and inspections to ensure product quality. While both roles require technical skills and work in related environments, their core responsibilities differ, with manufacturing associates involved in production and QC technicians in quality assurance.

What are the key skills and qualifications needed to thrive as a biomanufacturing associate?

To thrive as a Biomanufacturing Associate, you need a solid understanding of biotechnology, aseptic techniques, and good manufacturing practices (GMP), often supported by a degree in biology, chemistry, or related fields. Familiarity with bioprocessing equipment, batch record documentation, and quality control systems is typically required. Attention to detail, teamwork, and strong problem-solving skills help individuals excel in this role. These competencies ensure safe, consistent, and high-quality production of biopharmaceutical products in regulated environments.

What are some common challenges faced by biomanufacturing associates, and how can they be addressed?

Biomanufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), handling complex bioprocess equipment, and meeting tight production deadlines. These challenges can be managed by staying organized, following detailed protocols, and actively participating in ongoing training. Collaborating closely with team members and supervisors also helps ensure that any deviations or equipment issues are quickly identified and resolved, maintaining product quality and safety standards.
What are popular job titles related to Biomanufacturing Associate jobs in Ohio? For Biomanufacturing Associate jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biomanufacturing Associate jobs in Ohio look for? The top searched job categories for Biomanufacturing Associate jobs in Ohio are:
What cities in Ohio are hiring for Biomanufacturing Associate jobs? Cities in Ohio with the most Biomanufacturing Associate job openings:

Associate II, Quality Assurance (Night Shift)

RESILIENCE

West Chester, OH

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago


Job description

A career at Resilience is more than just a job - it's an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit www.resilience.com

Position Summary

This position is responsible for all QA activities that directly support execution of the process both within the Inspection, Assembly, Packaging (IDAP) operations, and in assigned areas outside of IDAP. These activities may include, but are not limited to, batch release, change control and documentation, equipment and process validation, deviation investigations, SOPs, supplier management, distribution center management, and regulatory interactions. At this level the incumbent is not necessarily performing all the essential job functions of the role immediately. The incumbent may begin by specializing in one or more of these responsibilities whilst working to develop a solid knowledge of the process being supported and applicable cGMPs. Over time the incumbent will be expected to obtain the necessary training to become skilled in all major responsibilities of the role.

Job Responsibilities

Maintain a high level of understanding of relevant production processes and quality systems

Perform the QA review and approval of the following GMP documentation that has direct impact on the activities performed by, and facilities utilized in their corresponding areas as applicable:

  • Change Requests
  • Batch Records and associated documentation
  • Product and Component Release transactions in SAP
  • Quality Investigations (Deviations, Product Complaints)
  • Validation Plans, Protocols and Reports
  • Standard Operating Procedures

Collaborate with and influences other Quality professionals across the organization to ensure consistent application and execution of key quality systems

Execute QA processes including batch record review, product disposition, and quality issue resolution to maintain the flow of products and documents to meet site objectives

Interface with applicable site support groups on projects (capital and non-capital) that impact the IDAP/assigned area, and proactively ensure GMP compliance during the planning, execution, and closeout phases of these projects

Collaborate with and influence other IDAP/assigned area members to facilitate process improvements and risk assessments; benchmark internal and external QA practices to identify innovative efficient and effective practices

Stay abreast of evolving regulatory compliance practices and recommend implementation strategies to site leaders

Collaborate in data analysis and report creation on quality metrics and key performance indicators

Hours (Night Shift):

  • 6 PM-6 AM
  • 2 nights on, 2 nights off, 3 nights on, 3 nights off and the rotation starts over


Minimum Qualifications

  • Experience in either the pharmaceutical industry, an operations environment, or Quality Assurance
  • Excellent oral and written communication skills
  • Strong ability and motivation to learn


Preferred Qualifications

  • Bachelor's degree; master's degree in science is desirable
  • Previous experience in a Lean, process-centric organization with an emphasis on continuous improvement
  • Multi-site / multi-functional experience

The work schedule listed reflects the employee's expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments.

Sponsorship or support for work authorization, including visas, is not available for this position.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.

Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $60,000.00 - $90,000.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.