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QC Inspection Analyst

About Forge  

Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most.   

Forge is based in Columbus, Ohio, in a 200,000 square foot facility known affectionately by team members as, the Hearth. The Hearth, is a custom-designed cGMP facility dedicated to AAV manufacturing and hosts scalable, end-to-end manufacturing services.  

 

About The Role  

We are currently seeking an Analyst I, Quality Control (Raw Materials) to join the Forge Biologics team. In this role, you will be responsible for conducting testing and evaluation of raw materials used in AAV vector production. Your work will involve executing various analytical tests per the processes defined within SOP documents in a cGMP compliant manner. Additionally, you will be responsible for performing comparisons between measured results and expected criteria and communicating those comparisons in a timely and thorough way. Your contribution will be essential in maintaining the integrity and safety of our gene therapy products.

What You'll Do:

  • Inspect all materials that arrive at the facility for integrity and quality.
  • Communicate between departments to ensure operations all have all required inspected materials.
  • Perform routine testing and analysis of raw materials using established protocols and analytical methods.
  • Conduct a range of tests, including but not limited to identity, purity, potency, and microbial contamination, on incoming raw materials.
  • Accurately document test results, observations, and procedures in accordance with Good Documentation Practices (GDP).
  • Collaborate with the procurement team to ensure timely receipt and testing of raw materials.
  • Escalate any non-conformance or deviations to appropriate channels for investigation and resolution.
  • Assist in the development and optimization of new testing methods and procedures.
  • Contribute to the maintenance, calibration, and qualification of laboratory equipment.
  • Adhere to Standard Operating Procedures (SOPs), cGMP guidelines, and regulatory requirements.
  • Maintain a clean and organized laboratory environment and adhere to safety protocols.

 

What You'll Bring:

  • Bachelor’s Degree in Biology, Biochemistry, Chemistry or a related discipline.
  • Familiarity with basic laboratory techniques and analytical methods.

Preferred Skills:

  • Prior experience in a laboratory or quality control environment.
  • Understanding of cGMP and regulatory guidelines.
  • Prior experience in a laboratory or quality control environment.
  • Understanding of cGMP and regulatory guidelines.

 

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. 

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. 

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. 

 

Life at Forge  

We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge’s core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by.  

HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. 

OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. 

PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. 

ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge’s vision, mission and goals. 

 

We’ve Got You Covered 

We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. 

  • Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents 
  • Flexible PTO (plus 14 paid company holidays) 
  • Annual bonus for all full-time employees
  • 401(K) company match
  • Fully-stocked kitchen with free food/drinks
  • 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care
  • Employee Assistance Program  
  • Wellness benefits (financial planning services, mental health counseling, employer paid disability)
  • Professional & Personal development resources - LinkedIn Learning, a dedicate training staff in-house, mentoring opportunities & access to leadership development coaches 

 

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Average salary estimate

$62500 / YEARLY (est.)
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$50000K
$75000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About QC Inspection Analyst, Forge Biologics

If you're on the lookout for a rewarding career in quality control, then the QC Inspection Analyst position at Forge Biologics in Columbus, Ohio might just be your ideal opportunity! Forge is not only a leading player in the gene therapy development arena, but it also crafts life-changing therapies alongside innovators within the medical community. As a QC Inspection Analyst, your main focus will be on ensuring the quality and integrity of the raw materials that are essential in producing AAV vectors—crucial components in gene therapy. You will carry out and document various analytical tests and evaluations of incoming materials to ensure they meet the rigorous standards set forth in our cGMP facility, affectionately known as the Hearth. Your responsibilities will range from inspecting and testing materials to collaborating with teams across the organization to keep production running smoothly. You'll communicate findings, maintain documentation according to Good Documentation Practices (GDP), and assist in optimizing testing methods. At Forge, we pride ourselves on our diverse and passionate culture, where employees are engaged in making a difference in patients' lives. So, if you’re excited about contributing to transformational medicines and growing your career in a collaborative environment, check out the QC Inspection Analyst role at Forge Biologics today!

Frequently Asked Questions (FAQs) for QC Inspection Analyst Role at Forge Biologics
What does a QC Inspection Analyst do at Forge Biologics?

As a QC Inspection Analyst at Forge Biologics, you will be responsible for inspecting and testing raw materials used in AAV vector production. This includes conducting various analytical tests and ensuring compliance with cGMP guidelines to maintain the quality and safety of our gene therapy products.

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What qualifications are needed for the QC Inspection Analyst position at Forge Biologics?

To be considered for the QC Inspection Analyst role at Forge Biologics, you should have a Bachelor’s Degree in Biology, Biochemistry, Chemistry, or a related field. Familiarity with laboratory techniques and prior experience in a quality control environment are preferred to help you excel in this position.

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How does Forge Biologics support its QC Inspection Analysts?

Forge Biologics is committed to the professional development and well-being of its QC Inspection Analysts. We offer a range of benefits, including flexible PTO, health insurance, wellness programs, and professional development resources to ensure you thrive in your role.

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What kind of testing will I be performing as a QC Inspection Analyst at Forge?

In your role as a QC Inspection Analyst at Forge, you'll engage in a variety of tests, including assessments of identity, purity, potency, and microbial contamination on incoming raw materials. This testing is crucial to uphold our commitment to quality in gene therapy manufacturing.

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What is the work environment like for a QC Inspection Analyst at Forge Biologics?

As a QC Inspection Analyst at Forge Biologics, you'll work in both a laboratory and an office environment. The role requires attention to detail and the use of personal protective equipment, especially when handling materials in clean room settings.

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What kind of growth opportunities are available for QC Inspection Analysts at Forge?

Forge Biologics values internal development, offering opportunities for QC Inspection Analysts to advance their careers. You can explore paths in quality assurance, laboratory management, or specialize further in analytical testing to enhance your professional journey.

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How does Forge Biologics ensure its QC Inspection Analysts adhere to industry regulations?

At Forge Biologics, we emphasize compliance with cGMP and regulatory guidelines. Our QC Inspection Analysts receive comprehensive training on Standard Operating Procedures (SOPs) and are guided in documentation practices to ensure all regulatory requirements are met consistently.

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Common Interview Questions for QC Inspection Analyst
Can you explain the importance of cGMP in the role of a QC Inspection Analyst?

It's essential to understand that cGMP stands for Current Good Manufacturing Practices. As a QC Inspection Analyst, adhering to these practices ensures that the products we test are manufactured consistently and controlled according to quality standards. In your answer, be prepared to discuss specific cGMP guidelines you have worked within.

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What analytical methods are you familiar with, and which ones would you apply as a QC Inspection Analyst?

When answering this question, highlight any specific analytical techniques you have used, such as HPLC, UV-Vis spectroscopy, or microbiological testing. Provide examples of when you utilized these methods in previous roles, explaining how they contributed to the quality assurance of products.

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How do you prioritize tasks when testing multiple raw materials?

In this response, convey the importance of effective prioritization based on material urgency, testing timelines, and compliance requirements. You might mention using checklists or software tools to track progress and deadlines while ensuring thorough documentation of results.

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Describe a time when you identified a deviation in test results. What steps did you take?

Detail a specific experience where you noticed an anomaly in testing. Discuss how you escalated the issue, conducted further investigations, consulted with team members, and helped develop corrective actions to resolve the deviation while documenting the process accordingly.

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What role does communication play in a QC Inspection Analyst’s responsibilities?

Emphasize that communication is vital for a QC Inspection Analyst. You'll need to effectively relay testing results, collaborate with diverse teams, and escalate issues, ensuring everyone is informed and can act swiftly to maintain quality standards.

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How do you ensure accuracy in documentation and reporting test results?

Highlight your adherence to Good Documentation Practices (GDP) and how you double-check your findings, maintain organized records, and use templates or software designed for compliance to ensure that all results are communicated clearly and accurately.

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What safety protocols do you follow in a laboratory environment?

Discuss specific safety protocols you are familiar with, such as wearing personal protective equipment, understanding chemical handling procedures, and maintaining a clean and organized workspace to ensure a safe laboratory environment.

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What experience do you have working in a team-based laboratory environment?

Illustrate your experience in collaborative settings, describing how you contributed to team goals, shared knowledge, assisted colleagues, and participated in group discussions to enhance laboratory efficiency and maintain product quality.

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How would you handle tight deadlines while ensuring the quality of testing?

Explain your approach to managing stress and prioritizing tasks effectively. You may discuss time management techniques, maintaining a steady pace through the workload, and ensuring quality checks are integrated even under pressure.

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What motivates you to work in quality control within the biotech industry?

Share your passion for ensuring patient safety and product quality within the biotech field. You can mention your desire to contribute to groundbreaking therapies and how working in quality control aligns with your personal and professional values in healthcare.

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Enable access to life changing gene therapies and help bring them from idea into reality.

16 jobs
MATCH
VIEW MATCH
FUNDING
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
SALARY RANGE
$50,000/yr - $75,000/yr
EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
November 29, 2024

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