Shoolin Inc is a staffing and technology solutions company specializing in tailored talent acquisition and recruitment excellence across Science, Engineering, Technology, Clinical & Life Sciences, and Pharmaceutical sectors. They provide skilled staffing, innovative tech solutions, and master vendor services, focusing on matching the right talent with organizational needs for both short-term projects and specialized roles. Their approach emphasizes cultural fit and long-term partnerships, positioning them as a transformative growth catalyst in workforce solutions with a commitment to quality and industry expertise.
Shoolin Inc is a staffing and technology solutions company specializing in tailored talent acquisition and recruitment excellence across Science, Engineering, Technology, Clinical & Life Sciences, and Pharmaceutical sectors. They provide skilled staffing, innovative tech solutions, and master vendor services, focusing on matching the right talent with organizational needs for both short-term projects and specialized roles. Their approach emphasizes cultural fit and long-term partnerships, positioning them as a transformative growth catalyst in workforce solutions with a commitment to quality and industry expertise.
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Job Title:
Quality Manager
Location:
Swiftwater, PA (Onsite)
Job Summary
We are seeking an experienced
Quality Manager
with a strong background in
pharmaceutical/biopharmaceutical manufacturing
, specifically in
vaccine and viral antigen production
. This role is onsite and requires solid leadership in
GMP Quality Systems
and
CAPA management
.
Required Qualifications
Key Responsibilities
Lead and manage
GMP-compliant Quality Systems
activities.
Oversee and drive
CAPA investigations
and ensure timely closure.
Support quality oversight of
biotech and vaccine manufacturing processes
, including viral antigen production.
Collaborate with cross-functional teams to ensure quality compliance.
Manage multiple projects and meet strict deadlines.
Bachelor’s degree
in engineering, life sciences, or a technical discipline (
Master’s preferred
).
6+ years of experience
in pharmaceutical/biopharmaceutical or related manufacturing environments.
Experience with vaccines
and knowledge of
viral antigen production
(
mandatory
).
Strong understanding of
GMP regulations
and quality system requirements.
Proven experience
leading CAPA activities
.
Proficiency with
LIMS, TrackWise, SAP
or similar quality systems.
Strong communication skills and high attention to detail.
Ability to manage multiple priorities and work under strict timelines.
Use systems such as
LIMS, TrackWise, and SAP
for quality and validation activities.
