Top 7 Glp research scientist Jobs in Columbus

GMP Senior Scientist
Andelyn Biosciences, Inc —Columbus, OH
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Paid parental leave
- Paid holidays
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14d
Chemist
Battelle —Columbus, OH
- Full-time
- Hybrid work
- Background check
- Bachelor of Science
- Bachelor's degree
- Wellness program
- Health insurance
Associate Director, Biomarker Science
Sarepta Therapeutics —Columbus, OH
- $152,800 - $191,000 a year
- Full-time
- Hybrid work
- Doctor of Philosophy
- US work authorization
- Senior level
12d
Environmental Toxicologist (Biochemist)
Battelle —West Jefferson, OH
- Full-time
- Hybrid work
- 5 years
- Bachelor of Science
- Pass drug screening
- Wellness program
- Health insurance
Technical Lead - Pharmaceutical Manufacturing Analytics
Battelle —Columbus, OH
- $128,800 - $183,600 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Doctor of Philosophy
- Wellness program
- Health insurance
Quality Assurance Technician
Tosoh Bioscience, Inc. —Grove City, OH
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Quick Apply
21h
Principal Toxicologist
Altria —United States
- $119,600 - $173,450 a year
- 5 years
- Analysis skills
- Presentation skills
- Profit sharing
- Paid parental leave

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Battelle —Columbus, OH
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GMP Senior Scientist
Andelyn Biosciences, Inc —Columbus, OH
Mentor and develop other Operations staff. Conduct adherent and suspension cell line scale-up to support ongoing large-scale manufacturing.
Quick Apply
14d
Chemist
Battelle —Columbus, OH
B.S. or M.S. degree in Chemistry, Material Science, Chemical Engineering, or related field. If applicable, Battelle will provide reasonable accommodations based…

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GMP Senior Scientist

Andelyn Biosciences, Inc -
Columbus, OH

Quick Apply

Job Details

Full-time
14 days ago

Benefits

Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Adoption assistance
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Loan assistance
Life insurance

Qualifications

Customer communication
Confidential information handling
Spreadsheets
Data reporting
Productivity software
Excel data analysis

Full Job Description

Overview of Andelyn Biosciences

Andelyn Biosciences is a biopharmaceutical Contract Development and Manufacturing Organization (CDMO) that specializes in advancing novel gene therapies from concept to commercialization. Located in Columbus, OH, the company operates out of the Andelyn Corporate Center (ACC) for clinical and commercial cGMP manufacturing of viral vectors and plasmids and the Andelyn Development Center (ADC) for preclinical non-cGMP activities.

Our Values are founded in our origin story.

The name “Andelyn” is a hybrid of two gene therapy patients who participated in pivotal Phase I clinical trials at Nationwide Children’s Hospital. Andrew received the first U.S. investigational gene therapy for Duchenne muscular dystrophy in 2006. Evelyn received experimental gene therapy for spinal muscular atrophy in 2015. “Andelyn” combines their names to represent all the families who have courageously participated in the research that makes today’s gene therapies possible.

Through this journey, we have been able to accelerate the development and manufacturing of innovative therapies to bring more treatments to more patients. We are Pioneering Solutions that Turn Hope into Reality™ through our ACCTSions.

ACCOUNTABLE in our actions.

CURIOUS to discover.

COMPASSIONATE in our thinking.

TRUSTWORTHY in our communications.

SUPPORTIVE of one another.

Employees are expected to perform the following essential functions under the framework of our ACCTSions.

What you will do.

The GMP Senior Scientist is responsible for leading production activities within a cGMP clean room environment. This role will closely collaborate with Operational Leadership on daily priorities and provide hands-on leadership for production activities, production, and project timelines, as well as staffing requirements. Senior Scientists are looked to be the subject matter experts and will ensure training, documentation, and regulatory and fiscal compliance.

Expect excellence from the production team. Lead from a position of influence, coaching, and collaboration alongside production staff.
Assign tasks to production staff to ensure schedules and metrics are met for client and company deliverables.
Conduct adherent and suspension cell line scale-up to support ongoing large-scale manufacturing.
Troubleshoot production issues, escalate all needs and provide potential resolutions to maintain successful production activities
Work with the supply chain to requisition and dispose of materials. Ensure material timelines are met to achieve production goals.
Create, lead, and manage change requests (CR) and corrective and preventive actions (CAPA) needed to ensure production changes and improvements are implemented in a timely manner.
Lead all aspects of the production documentation/client batch record requirements, adhering to GDP standards set forth by the company.
Regularly engage with QA staff and management to investigate deviations in manufacturing processes.
Actively engage with project teams to bring new projects and processes to GMP production in a timely manner.
Respond to equipment alarms for relevant areas, escalating issues as required to ensure product quality and safety.
Operate with high regard to all policies and procedures to ensure adherence to regulatory and quality standards.
Exercise great attention to detail, integrity, discretion, leadership, and personal responsibility.
Utilize clear and concise communication to deliver high productivity and contribute to the success of the team and its goals.
Moderate involvement in audits, inspection outcomes, and client communications.
Mentor and develop other Operations staff.
All other duties assigned.

What you bring to the team.

Must possess a relevant four-year degree OR relevant Masters OR relevant PhD, background in the life sciences, biotechnology or gene therapy industries preferred.
Working knowledge of team function within the organization.
First-level leadership. Coordinates and leads daily team activities. May spend a portion of time performing the work of those they supervise.
Prior supervisory experience is preferred.
Excellent detailed knowledge of cGMP, GLP, and FDA guidelines
Excellent communication, organization, and project management skills with the ability to manage multiple projects efficiently and adjust as priorities change.
Must be highly skilled in Microsoft Office (PowerPoint, Excel, Word), including data interpretation and reporting.
Ability to work independently as well as collaboratively in a diverse and inclusive work environment.
Must possess a client-focused mindset in daily tasks.
Must possess prior experience handling confidential information and the ability to maintain confidentiality.

What you can expect when working at Andelyn.

The pride of contributing to the development and manufacturing of life-saving therapies.
The invaluable experience of being a part of building the foundation of a new organization.

The opportunity to work alongside experts who have over 10 years in the gene therapy field.
Competitive compensation
Eligible on day one for medical, dental, and vision insurance plans with basic vision at 100% company-paid
160 hours of Paid Time Off annually
11 Company Paid Holidays plus 2 floating holidays annually.
Company Paid Life Insurance
401(k) Match
Company Paid short and long-term disability.
4 weeks of Paid Parental Leave for birth and adoption
Adoption Assistance
Tuition Reimbursement and Student Loan Repayment Assistance
Company Paid LinkedIn Learning access.
Employee Assistance Programs
Flexible work options (role specific)

Andelyn Biosciences embraces diversity and is an equal opportunity employer and does not discriminate based on race, religion, national origin, gender, gender identity, genetic information, sexual orientation, protected veteran status, disability, age, or another legally protected status. As an organization, we are committed to creating an environment where everyone ACCTS.

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glp research scientist jobs in columbus

GMP Senior Scientist

Chemist

Associate Director, Biomarker Science

Environmental Toxicologist (Biochemist)

Technical Lead - Pharmaceutical Manufacturing Analytics

Quality Assurance Technician

Principal Toxicologist

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