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Biotech Manufacturing Associate Jobs in Ohio (NOW HIRING)

Associate or bachelor's degree in Engineering, Facilities Management, or related technical field ... Experience in GMP-regulated pharmaceutical or biotech manufacturing facilities. * Certification ...

Packaging Associate - Day Shift

New Albany, OH · On-site

$14.50 - $17.75/hr

Pay Rate Low: 21.50 | Pay Rate High: 21.50 Our client, a renowned leader in biotechnology, is ... Requirements: * High school diploma or equivalent * 1+ years of experience in a manufacturing ...

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Biotech Manufacturing Associate information

See Ohio salary details

$11

$19

$31

How much do biotech manufacturing associate jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for biotech manufacturing associate in Ohio is $19.81, according to ZipRecruiter salary data. Most workers in this role earn between $15.53 and $22.16 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 Ohio? For Biotech Manufacturing Associate jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biotech Manufacturing Associate jobs in Ohio look for? The top searched job categories for Biotech Manufacturing Associate jobs in Ohio are:
What cities in Ohio are hiring for Biotech Manufacturing Associate jobs? Cities in Ohio with the most Biotech Manufacturing Associate job openings:
Infographic showing various Biotech Manufacturing Associate job openings in Ohio as of June 2026, with employment types broken down into 94% Full Time, 4% Part Time, 1% Contract, and 1% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $41,204 per year, or $19.8 per hour.
Maintenance Planner

Maintenance Planner

JLL

New Albany, OH

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago


JLL rating

8.2

Company rating: 8.2 out of 10

Based on 268 frontline employees who took The Breakroom Quiz

36th of 156 rated real estate companies


Job description

JLL empowers you to shape a brighter way.

Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented peopleand empowering them tothrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward.

Maintenance Planner - JLL

What this job involves:

The Maintenance Planner is responsible for planning, scheduling, and coordinating preventive, predictive, and corrective maintenance activities across Amgen's Ohio facilities. This role ensures that all maintenance work is executed safely, efficiently, and in compliance with GMP, regulatory, and corporate standards.

The Planner works closely with maintenance technicians, engineering, operations, and vendors to optimize asset reliability, minimize downtime, and support production continuity within a highly regulated pharmaceutical environment.

A hospitality mindset is fundamental to delivering exceptional workplace experiences for our client. We seek candidates who excel in collaborative environments, communicate effectively with diverse stakeholders, manage multiple priorities simultaneously, maintain high standards of accuracy, and adapt quickly to resolve challenges.

What your day-to-day will look like:

Maintenance Planning & Scheduling

  • Develop detailed work plans for preventive, predictive, and corrective maintenance activities.

  • Build and maintain weekly and shutdown maintenance schedules in coordination with site operations and production teams.

  • Ensure proper sequencing, resource allocation, and prioritization of work orders based on risk, asset criticality, and business impact.

  • Maintain backlog management processes, ensuring work orders are appropriately prioritized, scoped, and executed.

CMMS / Asset Management

  • Utilize CMMS (e.g., Maximo, SAP PM, or similar) to plan, schedule, and track maintenance activities.

  • Create and maintain accurate equipment records, BOMs, job plans, and standard operating procedures.

  • Ensure data integrity for all maintenance documentation, including labor hours, parts usage, and completion notes.

Preventive & Predictive Maintenance

  • Support development and continuous improvement of preventive maintenance (PM) programs.

  • Optimize maintenance frequencies and procedures using reliability-centered maintenance (RCM) principles.

  • Coordinate predictive maintenance strategies (vibration, thermography, etc.) to prevent equipment failures.

Work Coordination

  • Collaborate with maintenance supervisors and technicians to ensure readiness of scheduled work (parts, tools, permits, permits, and documentation).

  • Coordinate with reliability engineers, validation, quality, and EHS teams for regulated maintenance activities.

  • Plan and support outages, shutdowns, and major maintenance events.

Materials & Vendor Coordination

  • Identify and ensure availability of spare parts, tools, and materials before work execution.

  • Coordinate with procurement and storeroom teams to maintain optimal inventory levels.

  • Interface with third-party vendors and contractors for specialized maintenance activities.

Compliance & Safety

  • Ensure all maintenance activities are planned in compliance with GMP, FDA, OSHA, and Amgen quality standards.

  • Incorporate safety requirements into all job plans, including lockout/tagout (LOTO), confined space, and permit requirements.

  • Support audit readiness and participate in inspections and compliance reviews.

Continuous Improvement

  • Analyze maintenance KPIs (PM compliance, schedule adherence, backlog, downtime, etc.) and recommend improvements.

  • Drive standardization of job plans and best practices across the site.

  • Participate in root cause analysis (RCA) and reliability improvement initiatives.

Required Qualifications:
  • Associate or bachelor's degree in Engineering, Facilities Management, or related technical field (or equivalent experience).

  • 3-7+ years of experience in maintenance planning, scheduling, or maintenance supervision in an industrial or regulated environment (pharma, biotech, or similar preferred).

  • Experience using CMMS platforms (Maximo, SAP, or similar).

  • Strong knowledge of mechanical, electrical, and HVAC systems in a critical facility environment.

Preferred Qualifications:

  • Experience in GMP-regulated pharmaceutical or biotech manufacturing facilities.

  • Certification such as Certified Maintenance & Reliability Professional (CMRP) or equivalent.

  • Experience with reliability-centered maintenance (RCM) or Lean maintenance practices.

  • Familiarity with cleanrooms, utilities (WFI, clean steam), and critical systems.

Key Competencies

  • Strong planning, organization, and prioritization skills

  • High attention to detail and documentation accuracy

  • Ability to work cross-functionally in a matrixed environment

  • Knowledge of regulatory compliance (GMP, FDA)

  • Data-driven decision making and problem-solving

  • Excellent communication and stakeholder management skills

Work Environment

  • Based at a Pharmaceutical facility (New Albany area)

  • Combination of office planning work and field coordination in active maintenance and production areas

  • Requires adherence to PPE, safety standards, and cleanroom requirements

Reporting Structure

  • Reports to: Facility Manager

  • Works closely with:

    • Amgen Facilities, Engineering, and Manufacturing teams

    • JLL maintenance technicians and supervisors

    • Quality, EHS, and Validation teams

Location:

On site - New Albany, OH

Work Shift:

Monday to Friday 7:00am to 3:30pm + Overtime based on business needs

Salary/ Comp:

$60,800 - $88,200 | $29,23 - $42,40 + Overtime based on business needs.

At JLL, we are collectively shaping a brighter way - for our clients, ourselves and our fellow employees. We choose to take the more inspiring, innovative, and optimistic path on our journey toward success. What sets JLL apart is our culture of collaboration, locally and across the globe, which allows us to create transformative solutions for the real estate industry. We support each other's wellbeing and champion inclusivity and belonging across teams.

JLL is an Equal Opportunity Employer committed to diversity and inclusion.

This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without sponsorship.

Location:

On-site -New Albany, OH

If this job description resonates with you, we encourage you to apply, even if you don't meet all the requirements. We're interested in getting to know you and what you bring to the table!


Personalized benefits that support personal well-being and growth:

JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits may include:

  • 401(k) plan with matching company contributions

  • Comprehensive Medical, Dental & Vision Care

  • Paid parental leave at 100% of salary

  • Paid Time Off and Company Holidays

  • Early access to earned wages through Daily Pay

At JLL, we harness the power of artificial intelligence (AI) to efficiently accelerate meaningful connections between candidates and opportunities. Using AI capabilities, we analyze your application for relevant skills, experiences, and qualifications to generate valuable insights about how your unique profile aligns with the specific requirements of the role you'repursuing.

JLL Privacy Notice

Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely.

For more information about how JLL processes your personal data, please view our Candidate Privacy Statement.

For additional details please see our career site pages for each country.

For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here.

Jones Lang LaSalle ("JLL") is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process - including the online application and/or overall selection process - you may email us at HRSCLeaves@jll.com. This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page > I want to work for JLL.

Accepting applications on an ongoing basis until candidate identified.


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