687 Biotech Lab jobs in Philadelphia,PA

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Director, Quality (GCP/GCLP/GVP)

LARIMAR THERAPEUTICS

Philadelphia, PA 19102

Paid Time OffRetirement Benefit

Bachelor's degree in life sciences
Minimum of 10+ years experience in a Quality role supporting Clinical Operations and/or Pharmacovigilance departments within a biotechnology or pharmaceutical environment
Experience managing GCP/GCLP/GVP quality processes, including risk management activities
Demonstrated experience managing GCP inspections, including preparation and response activities
Minimum of 3 years experience performing GCP/GCLP/GVP audits or comparable GxP audit experience
Expert knowledge of GxP systems, quality principles, and GCP/GCLP/GVP regulations (FDA, MHRA, EMA, etc.) and guidance documents (GCP/ICH)
Demonstrated ability to initiate process improvements and take initiative
Must possess a strong attention to detail while having the ability to work independently and collaboratively, as required, in a fast-paced environment

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MoFe Engineer I

Sightpath Medical

Philadelphia, PA 19102

$28-$34/hr

OnsiteHealth InsurancePaid Time OffRetirement Benefit

Technical Degree: Degree in Laser Electro-optics, Biomedical Equipment Technology, Electronics, or a similar field; military training in related fields is also acceptable.
Hands-On Experience: Proficiency with basic electronics and test equipment.
Driving Record: Able to produce a valid driver's license and pass a Motor Vehicle Report (MVR)/ driving record.
Physical Demands: Ability to lift up to 100 lbs. and stand for extended periods.

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Director, Regulatory Affairs, Ex-US

LARIMAR THERAPEUTICS

Philadelphia, PA 19102

OnsiteUrgently Hiring

Minimum of 4-year undergraduate degree
5 to 8 years' experience in a Regulatory Affairs role in the pharmaceutical industry, experience with EMA, MHRA and other local European agencies preferred
Understanding of GxP systems and Quality principles
Ability to research global regulatory guidance (nonclinical, clinical and CMC) and precedence to assist in the development and execution of global regulatory strategies
Experience with preparation (authoring and review) of documents for global Health Authority submissions including but not limited to IND amendments, CTA submissions, Global Health Authority Meeting packages and global marketing authorization applications
Excellent communication, time management and project management skills
Continuous quality improvement mindset and attention to details
Can do attitude, flexibility, and mental agility

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Computer Field Technician

U.S. Navy

Haddonfield, NJ 08033

New, Posted 1 day ago

Maintenance Technician

VitalCore Health Strategies

Wilmington, DE 19886

Bilingual Preferred

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Senior Manager, Project Management, Tech Ops

CSL Behring

King of Prussia, PA 19406

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Service Technician - Commercial Swimming Pools

Main Line Commercial Pools

King of Prussia, PA 19406

$20-$30/hr

New, Posted 5 hours ago

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Mobile Trailer Technician/Service Truck Technician

TEN Transportation Equipment Network

Fairless Hills, PA 19030

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Laboratory Technical Specialist III - Hematology/Coag

ChristianaCare

Wilmington, DE 19805

OnsiteHealth InsurancePaid Time OffRetirement Benefit

BS MLS (ASCP) or equivalent (ASCLS, CLIS, AMT, MT)
Minimum five years' experience in area of expertise, with one year in supervisory or leadership position
At least one year of leadership, supervisory, lead technologist, or technical specialist experience
Strong knowledge of clinical laboratory instrumentation, quality systems, troubleshooting, and regulatory requirements
Aspiring to or capable of leading, mentoring, and developing staff (implied by leadership experience)

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Field Applications Scientist

MaxCyte

Philadelphia, PA 19102

OnsiteHealth InsurancePaid Time Off

MS or PhD in bioengineering, cell biology, molecular biology, biochemistry or related field.
Recent hands-on experience in mammalian cell culture essential (primary cells/T cells preferred).
3+ years in one or more: genome editing (e.g., CRISPR/Cas9), cell therapy development, immunology, protein/viral expression, or process development.
Experience in large scale cell culture and/or high throughput cell-based screening would be beneficial.
Practical knowledge of on-/off-target assessment workflows and analytics is a strong plus.
Demonstrated troubleshooting ability and experimental design/data interpretation skills.
Customer-facing experience (FAS, applications, technical support, or similar) preferred.
Robust trouble shooting skills.
Confident communicator—able to present to scientific and executive audiences; strong writing and documentation discipline.
Core competencies: Scientific rigor with a solution-oriented, hands-on mindset. Clear, audience-appropriate communication and teaching. Cross-functional collaboration (Sales, Product, Service, Marketing). Organization, ownership, and reliable follow-through.
Comfortable with CRM (e.g., SFDC), standard data analysis tools, and documentation best practices.
Entrepreneurial mindset: Proven ability to thrive in an entrepreneurial, high-growth environment, demonstrating strategic thinking, problem-solving, and self-motivation.
Customer-centric leadership: Builds and maintains strong customer relationships, demonstrating passion for the company's mission and solutions.
Ability to travel ~ 50-70% within territory, occasional conferences/customer visits outside territory.
Work Setup: Field-based with regular onsite customer engagements; close alignment with Sales and the global FAS team.