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QA Document Specialist (FT)
Integral Molecular Philadelphia, PA
$69k-85k (estimate)
Full Time | Scientific Services 5 Months Ago
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Integral Molecular is Hiring a QA Document Specialist (FT) Near Philadelphia, PA

Integral Molecular is a close-knit, medium-sized company composed of smart, curious scientists. Based in Philadelphia, we are focused on developing and applying innovative technologies that advance vaccines and antibody therapeutics targeting difficult proteins.
As we are actively growing, we are looking for our first Quality Assurance Associate to establish and develop a robust quality assurance system from the ground up. This individual will play a crucial part in ensuring the quality and reliability of our products by designing, implementing, and managing company-wide quality processes and procedures across the company. A desirable candidate will be highly organized, self-reliant when executing tasks, and contribute as a collaborative, supportive team member.
Opportunities that this position offers you:
  • Opportunity for ground-floor development of the Quality Management System for a biotech company that has significant societal impact.
  • Involvement with the company’s journey to obtain ISO 9001 certification.
  • Ownership of the QMS and all certifications moving forward.
  • Collaboration with cross-team scientists and project leaders.
What you will do at Integral Molecular:
  • Implement standards and define quality processes and procedures through controlled documentation completion and system management.
  • Efficiently manage CAPA plans, data, and quality improvement initiatives.
  • Lead the company through internal and external audits, including audit preparation, execution, and follow-up actions.
  • Track and oversee all commitments for actions or changes made from previous customer audits.
  • Keep records of all qualification and validation activities performed for critical equipment.
  • Assist in the evaluation of designated vendors and/or out-sourced activities.
The ideal candidate will have:
  • BS in a science-related field; molecular biology, biochemistry, chemistry, biology, etc.
  • 2 years of relevant experience, including Quality and Logistics experience in biotechnology industry experience a plus.
  • Previous experience in Quality Management Systems with an eye for details.
  • Knowledge of ISO 9001, ISO 13485 and/or FDA GMP/GLP is a plus.
  • Good interpersonal skills.
  • A sense of urgency to complete assignments on time.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Scientific Services

SALARY

$69k-85k (estimate)

POST DATE

12/25/2023

EXPIRATION DATE

05/17/2024

WEBSITE

integralmolecular.com

HEADQUARTERS

PHILADELPHIA, PA

SIZE

50 - 100

FOUNDED

2001

TYPE

Private

CEO

BENJAMIN DORANZ

REVENUE

<$5M

INDUSTRY

Scientific Services

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About Integral Molecular

Integral Molecular is a biotechnology firm that develops and commercializes therapeutic antibodies for the treatment of cancer and diabetes.

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The following is the career advancement route for QA Document Specialist (FT) positions, which can be used as a reference in future career path planning. As a QA Document Specialist (FT), it can be promoted into senior positions as a System Documentation Specialist II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary QA Document Specialist (FT). You can explore the career advancement for a QA Document Specialist (FT) below and select your interested title to get hiring information.