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Manager Biological Control Jobs in Ohio (NOW HIRING)

Mp Biomedicals

QC Lab Technician 1

Solon, OH · On-site

$50K - $52K/yr

... Product Manager or designee. * Support quality investigations and QA verifications as directed ... Bachelor's degree in Biology, Chemistry, Molecular Biology, or Biochemistry * Entry level; prior ...

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Voyage Foods

Quality Control Supervisor

Mason, OH · On-site

$80 - $120/hr

... Manager as appropriate. * Support document control processes, including SOPs and work instructions. Required Experience: Required * Bachelor's degree in Food Science, Biology, or related field; or ...

Voyage Foods

Quality Control Supervisor

Mason, OH · On-site

... Manager as appropriate. * Support document control processes, including SOPs and work instructions. Required Experience: Required * Bachelor's degree in Food Science, Biology, or related field; or ...

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All JobsBiological Control JobsManager Biological Control JobsManager Biological Control Jobs in Ohio

Manager Biological Control information

What are the key skills and qualifications needed to thrive as a manager biological control?

To thrive as a Manager Biological Control, you need expertise in entomology, integrated pest management, and agricultural science, often supported by a relevant degree and experience in biological control programs. Familiarity with laboratory and field research tools, data analysis software, and regulatory compliance systems is typically required. Strong leadership, problem-solving, and communication skills are essential for managing teams and collaborating with stakeholders. These skills ensure effective implementation of sustainable pest management strategies, regulatory adherence, and successful project outcomes.

What is a manager biological control?

A Manager Biological Control oversees programs and teams dedicated to managing pests and invasive species using natural predators, parasites, or pathogens instead of chemicals. They are responsible for planning, implementing, and monitoring biological control strategies within agricultural, horticultural, or environmental settings. Their duties include coordinating research, ensuring regulatory compliance, managing staff, and communicating with stakeholders to promote sustainable pest management solutions.

What are some common challenges faced by a manager biological control and how can they be addressed?

A Manager Biological Control often encounters challenges such as balancing effective pest management with environmental sustainability and ensuring compliance with regulatory standards. Coordinating field trials, managing a diverse team of scientists and technicians, and keeping up with emerging biological control technologies can also be demanding. Successful managers address these challenges by fostering strong communication within multidisciplinary teams, staying updated on industry best practices, and building relationships with regulatory agencies and research partners. Regular training and adopting integrated pest management strategies can also help navigate these complexities.

What is the difference between Manager Biological Control vs Biological Control Specialist?

AspectManager Biological ControlBiological Control Specialist
CredentialsBachelor's or Master's in entomology, biology, or related field; certifications may be preferredSimilar educational background; certifications often beneficial
Work EnvironmentSupervises teams, manages projects, collaborates with research and field staffConducts field and laboratory research, implements biological control methods
Employer & Industry UsageUsed in agricultural, horticultural, and pest management companiesEmployed in research institutions, pest control firms, agricultural companies

The main difference is that the Manager Biological Control oversees teams and projects, focusing on strategy and management, while the Biological Control Specialist primarily conducts research and implements biological pest control methods. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What are the most commonly searched types of Biological Control jobs in Ohio? The most popular types of Biological Control jobs in Ohio are:
What are popular job titles related to Manager Biological Control jobs in Ohio? For Manager Biological Control jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Manager Biological Control jobs in Ohio look for? The top searched job categories for Manager Biological Control jobs in Ohio are:
What cities in Ohio are hiring for Manager Biological Control jobs? Cities in Ohio with the most Manager Biological Control job openings:
Manager Biological Control jobs near you
Infographic showing various Manager Biological Control job openings in Ohio as of August 2026, with employment types broken down into 80% Full Time, 19% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Scientist I, QC Analytical

Forge Biologics

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job description

Forge Your Future with Us:
At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities - all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins.
Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen - you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases.
What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely, and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together.
At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us.
If you're ready to use your talent to help deliver hope to patients around the world, join us - and be part of something bigger than yourself.
About the Role:
The Scientist I, Quality Control (Analytical) role will primarily focus on analytical method execution, method qualification, method validation, and troubleshooting efforts. This position will be responsible for executing in-process, final product, and stability testing for AAV vectors, plasmids, and microbial and mammalian cell banks, while ensuring that activities occur in an efficient and cGMP compliant manner. This role will function as a subject matter expert (SME) for either nucleic acid-based methods (e.g. ddPCR, qPCR), protein-based assays (e.g. CE, AUC), or cell-based assays (e.g. TCID50, potency). This position will also be responsible for fostering innovation within the QC department, either independently or by partnering with Analytical Development, ensuring cutting edge technologies are employed to maintain the highest QC standards in the analysis of gene therapy products. This role provides an opportunity to play a significant impact in the success of client gene therapy programs.
Responsibilities:
  • Perform in-process, release, and stability testing for assays relevant to viral vector/gene therapy products, plasmids, and cell banks, including in-process testing, lot release testing, assay qualification, and validations.
  • Function as an SME for either nucleic acid-based methods (e.g. ddPCR, qPCR), protein-based assays (e.g. CE, AUC), or cell-based assays (e.g. TCID50, potency). Additionally, perform advanced analytical testing quality control assays, including compendial testing, ELISA, and viability assays, to assess the quality, potency, and safety of AAV vector products.
  • Support troubleshooting of processes/assays as an SME. Represent QC as a SME during audits and inspections.
  • Ensure effective qualifications, validations, and transfer of analytical methods to Quality Control in a phase-appropriate fashion, to support pre-clinical, clinical, and commercial activities.
  • Contribute to authoring and/or reviewing QC documentation, including but not limited to: SOPs, analytical methods and forms, qualifications protocols, and validation protocols.
  • Conducts thorough investigations to determine root cause of OOS investigations and other non-conforming results and implements appropriate corrective and preventative actions in a timely manner.
  • Provide support for Deviations, Change Controls, and CAPAs related to in process and final product testing.
  • Review and approve GMP documentation associated with in process, final product, and stability testing.
  • Drive the development, optimization, and validation of novel analytical methods to enhance quality control processes.
  • Provide technical guidance and mentorship to junior team members, promoting their personal growth and skill development.
  • Compile data with minimal oversight, generating reports, and archiving assay data; responsible for performing the analysis and interpretation of assay results.
  • Support regulatory and client inspections and internal audits of GMP systems.
  • Manage tracking and trending of in process and final product testing data, including, but not limited to; leading/participating in out of specification (OOS)/out of trend (OOT) Laboratory Investigations.

Qualifications:
  • Bachelor's, Master's, or PhD or in a relevant scientific field (e.g., biology, biochemistry, molecular biology). Advanced degree preferred.
  • SME for either nucleic acid-based methods (e.g. ddPCR, qPCR), protein-based assays (e.g. CE, AUC), or cell-based assays (e.g. TCID50, potency) based on experience. Advanced knowledge of complex molecular biology, biochemistry, or cell biology techniques and analytical methods (e.g., qPCR, cell-based infectivity assays, potency assays).
  • Proven ability to execute, troubleshoot, and optimize analytical assays.
  • Strong analytical and data interpretation skills to assess and drive quality improvement through the analysis of quality metrics and performance data.
  • Robust understanding of cGMP requirements as they pertain to Quality Control and Analytical Development testing.
  • Experience in leading, mentoring, and guiding junior team members.
  • Experience with electronic Quality Management Systems (EQMS), Laboratory Information Management Systems (LIMS), etc.

Work Environment and Physical Demands
This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area.
Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
We've Got You Covered:
At Forge Biologics, we believe our people deserve to be taken care of - in and out of the workplace. We've built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:
Health from day one
  • Health, dental and vision insurance start your first day - with 90% of premiums covered for you and your family.

Time to recharge
  • A competitive paid time off plan - because rest fuels innovation.
  • 12 weeks of fully paid parental leave so you can focus on family when it matters most.

Rewarding your impact
  • Annual bonus opportunities for all full-time team members.
  • 401(k) with company match to help you plan for the future.
  • Special employee discounts, including childcare and dependent care savings.

Your wellness, supported
  • Onsite fitness facility at The Hearth.
  • Mental health counseling and financial planning services through our Employee Assistance Program.
  • Employer-paid short and long-term disability coverage to protect your peace of mind.

Fuel for your workday
  • A fully stocked kitchen with free snacks and beverages - we keep you energized and ready for what's next.

Grow with us
  • Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge.

Apply