Top 6 Microbiology supervisor Jobs in Allentown Pa

Senior Manager, Quality Control
Piramal Pharma Solutions —Sellersville, PA
- Full-time
- Microsoft Word
- 7 years
- Bachelor's degree
Quick Apply
Supervisor, Microbiology
QuVa Pharma —Bloomsbury, NJ
- $74,766 - $102,817 a year
- Bachelor of Science
- Bachelor's degree
- Mentoring
- Paid holidays
- Health insurance
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Assistant Manager, Packaging Quality Assurance
The Boston Beer Company —Breinigsville, PA
- $82,000 - $141,000 a year
- Overtime
- Mid-level
- Ability to climb stairs
- Ability to lift 50 pounds
- Wellness program
- Employee stock purchase plan
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QUALITY MANAGER
FRAGRANCE MANUFACTURING INC —Allentown, PA
- Full-time
- Microsoft Outlook
- Engineering
- ERP systems
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Quality Assurance Supervisor
Bakerly Barn LLC —Easton, PA
- Full-time
- Writing skills
- Mid-level
- 3 years
- Paid holidays
- Disability insurance
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13d
Manager, Quality & Food Safety-Low Acid Aseptic Food
Sunny Sky Products LLC —Douglassville, PA
- Weekends as needed
- 5 years
- Microsoft Office
- Supervising experience
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Senior Manager, Quality Control

Piramal Pharma Solutions -
Sellersville, PA

Quick Apply

Job Details

Full-time

Qualifications

Data visualization software proficiency
Microbiology
Presentation software
GMP
Project management experience in manufacturing
Microbiology
Bachelor's degree
Gas chromatographs
Leading team collaboration initiatives
Managing projects
Manufacturing
Project leadership
Stakeholder relationship building
Senior leadership
Stakeholder management

Full Job Description

Job Overview
Provides strategic and operational Quality Control (QC) leadership for laboratory operations spanning Phase 2 clinical development through Commercial manufacturing. Accountable for project management of laboratory operations, including schedule planning, schedule adherence, and execution against manufacturing and supply chain timelines. Leads the development and use of dashboards for sample management, throughput, and On-Time-In-Full (OTIF) performance metrics.

Responsible for planning, coordination, and execution of QC activities across raw material testing, commercial product testing, stability programs, analytical and cleaning method development, and method transfers. Accountable for achieving QC targets and KPIs, managing budgets, and developing a high-performing, cross-trained QC organization with robust succession and backup coverage for critical roles.

Key Roles & Responsibilities:

Laboratory Operations & Project Management

Provides end-to-end laboratory operations management from Phase 2 clinical development through Commercial production
Leads project management of laboratory activities, ensuring alignment with manufacturing schedules, regulatory commitments, and product launch timelines
Develops and manages laboratory master schedules, including sample planning, resource loading, and schedule adherence
Ensures laboratory deliverables are completed On Time In Full (OTIF) in support of manufacturing, release, stability, and regulatory submissions
Creates and maintains operational dashboards to track:

Sample throughput

Testing cycle times

OTIF performance

Capacity utilization and backlog

Proactively identifies risks to timelines and implements mitigation plans

Testing & Technical Oversight

Oversees physical, chemical, and microbiological testing of:

Raw materials

In-process and finished products

Stability samples

Special and investigational samples

Provides oversight for:

Raw material qualification and testing

Commercial product release testing

Stability testing programs

Ensures accurate documentation, review, and submission of raw data and results in LIMS
Oversees preparation of reagents and microbiological media, including growth promotion testing
Provides technical oversight for advanced analytical techniques, including:

HPLC, UPLC, GC, ICP-MS

Ensures data integrity and compliance through robust data review and lot disposition support

Method Development, Validation & Transfer

Leads and oversees:

Analytical method development

Analytical method validation and verification

Analytical method transfer (internal and external)

Cleaning method development

Cleaning method validation and transfer

Provides technical and strategic oversight for new product introductions and lifecycle management activities
Ensures method readiness to support clinical progression, commercialization, and post-approval changes

Quality Systems, Compliance & Investigations

Leads laboratory OOS, OOT, and atypical investigations, ensuring timely, compliant, and scientifically sound conclusions
Provides compliance leadership and subject matter expertise for the QC department
Supports and sustains a continuous audit readiness program to ensure inspection-ready state at all times
Continuously monitors and improves QC systems and procedures to enhance:

Regulatory compliance

Data integrity

Operational efficiency

Industry best practices

Supports QC Systems Administration activities, including Empower, LIMS, and TrackWise
Support Vendor Audits as the SME for third party laboratories

Leadership, Talent Development & Continuous Improvement

Effectively leads and coaches QC staff and lab management to achieve departmental goals
Establishes daily priorities and allocates resources to meet operational and project needs
Develops and executes analyst training and cross-training programs
Conducts performance and development reviews and determines merit increases
Recruits, interviews, and hires qualified technical and support staff
Drives continuous improvement initiatives to enhance laboratory efficiency, throughput, and right-first-time performance
Represents QC on site-level and cross-functional project teams

Budget & Capital Management

Prepares, manages, and administers the QC laboratory operating and capital budgets
Tracks budget performance against plan and implements corrective actions as needed
Oversees implementation of key laboratory projects, including:

LIMS deployments and enhancements

TrackWise implementations

Equipment qualification (IOPQ/PQ)

Capacity expansion initiatives

Responsibilities

Provide strategic leadership and operational execution for QC laboratory activities
Ensure laboratory schedules, deliverables, and metrics align with business and regulatory needs
Maintain a compliant, efficient, and inspection-ready QC organization
Develop talent, build bench strength, and promote a culture of accountability and continuous improvement

Qualifications & Experience

Bachelor’s degree in Chemistry, Biology, Microbiology, or related scientific discipline (advanced degree preferred)
Minimum 10 years of technical experience and 7 years of leadership experience in a GMP-regulated environment
Experience in a CDMO environment preferred.
Demonstrated project management experience within laboratory operations
Strong written, verbal, and interpersonal communication skills
Proficiency with Microsoft Word, Excel, PowerPoint, and data visualization for dashboards and metrics
Strong background in analytical chemistry and/or microbiological testing
Expertise with HPLC, UPLC, and GC systems
Proven leadership capabilities, including:

Building effective teams

Strategic mindset and business insight

Problem-solving and decision-making

Resource and stakeholder management

Change leadership and execution

Job Type: Full-time

Education:

Bachelor's (Required)

Ability to Commute:

Sellersville, PA 18960 (Required)

Work Location: In person

Quick Apply

Refine Your Search

microbiology supervisor jobs in allentown pa

Senior Manager, Quality Control

Supervisor, Microbiology

Assistant Manager, Packaging Quality Assurance

QUALITY MANAGER

Quality Assurance Supervisor

Manager, Quality & Food Safety-Low Acid Aseptic Food

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