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Biotech Operations Manager Jobs in Pennsylvania (NOW HIRING)

Prism Biotech

Staff Accountant

King Of Prussia, PA · On-site

$54K - $72K/yr

This person will manage all accounting procedures to ensure Prism Biotech's overall financial ... operations. Requirements: * Bachelor's degree in accounting or related field * Strong math skills

Prism Biotech, Inc

Staff Accountant

King Of Prussia, PA · On-site

$54K - $72K/yr

This person will manage all accounting procedures to ensure Prism Biotech's overall financial ... operations. Requirements: * Bachelor's degree in accounting or related field * Strong math skills

PSC Biotech

Microbiologist

York, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Experience With operations spanning the globe and featuring a multi-cultural team, BioTechnique ... Ability to manage multiple priorities and work effectively in a team environment. Demonstrated ...

Krystal Biotech

Clinical Scientist

Pittsburgh, PA · On-site

Assists Clinical Operations in assuring adherence to Good Clinical Practice, investigator integrity ... to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes.

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Showing results 21-40

All JobsBiotech Operations JobsBiotech Operations Manager JobsBiotech Operations Manager Jobs in Pennsylvania

Biotech Operations Manager information

See Pennsylvania salary details

$31.1K

$63.6K

$118.8K

How much do biotech operations manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for biotech operations manager in Pennsylvania is $63,609.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,100.00 and $77,700.00 per year, depending on experience, location, and employer.

What does a Biotech Operations Manager do?

A Biotech Operations Manager is responsible for overseeing the daily operations of biotechnology facilities, ensuring that production processes run efficiently and comply with industry regulations. They manage teams, coordinate schedules, oversee supply chains, and implement quality control measures. Additionally, they work closely with research and development, regulatory, and quality assurance teams to ensure products meet all safety and efficacy standards. Their role is crucial in maintaining productivity, safety, and compliance in a biotech organization.

What are the key skills and qualifications needed to thrive as a Biotech Operations Manager, and why are they important?

To thrive as a Biotech Operations Manager, you need a solid background in life sciences, business management, and regulatory compliance, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and project management tools is typically required, along with certifications like Six Sigma or PMP being advantageous. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for managing teams and cross-functional projects. These skills ensure efficient operations, regulatory adherence, and successful product delivery in the highly regulated biotech industry.

What are some common challenges faced by Biotech Operations Managers, and how can they be addressed?

Biotech Operations Managers often face challenges such as maintaining regulatory compliance, managing cross-functional teams, and ensuring smooth production processes. These challenges can be addressed by staying updated on industry regulations, fostering clear communication between departments, and implementing robust quality control systems. Additionally, leveraging project management tools and continuous process improvement strategies can help streamline operations and minimize risks.

What is the difference between Biotech Operations Manager vs Biotech Laboratory Supervisor?

AspectBiotech Operations ManagerBiotech Laboratory Supervisor
CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; experience in biotech operationsBachelor's or Master's in Life Sciences; laboratory management experience; relevant certifications often preferred
Work EnvironmentOversees multiple departments, manages projects, and ensures compliance across operationsManages daily lab activities, supervises lab staff, and maintains lab safety and procedures
Employer & Industry UsageUsed in biotech companies for operational oversightCommon in research labs, biotech firms, and pharmaceutical companies for lab management

The Biotech Operations Manager focuses on overseeing overall biotech operations, including project management and compliance, while the Biotech Laboratory Supervisor concentrates on managing daily lab activities and staff. Both roles require relevant scientific credentials, but their scope and responsibilities differ significantly.

What are popular job titles related to Biotech Operations Manager jobs in Pennsylvania?

For Biotech Operations Manager jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Biotech Operations Manager jobs in Pennsylvania look for?

The top searched job categories for Biotech Operations Manager jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Biotech Operations Manager jobs?

Cities in Pennsylvania with the most Biotech Operations Manager job openings:

Biotech Operations Manager jobs near you
Infographic showing various Biotech Operations Manager job openings in Pennsylvania as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $63,609 per year, or $30.6 per hour.

Clinical Trial Associate/Clinical Research Coordinator

Krystal Biotech

Pittsburgh, PA • On-site

$32.50 - $44.50/hr

Full-time

Re-posted 25 days ago

Job description

Clinical Trial Associate/Clinical Research Coordinator
About Krystal Bio:
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our Clinical Operations Team. The Associate's responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods.
Primary Responsibilities:
  • Assists clinical trial team with preparation, handling, distribution and tracking of clinical trial supplies and other study supplies
  • Ensure proper documentation and protocol and regulatory practices are being followed
  • Establish relationships with and work with trial sites to ensure study materials and documentation are being handled appropriately
  • Work with accounting/finance to help establish budgets, track invoices, approve vendor activity and assists with budget reconciliation
  • Train investigative site staff on protocol responsibilities, Investigational Product accountability and study documentation
  • Monitor investigative sites according to Good Clinical Practice and applicable regulations - site visits may include, site qualification, initiation, monitoring and close outs
  • Provides support for inspection readiness by formatting, proofreading documents and contributing to the establishment, maintenance, and quality control of the TMF
  • Review investigative site SOPs to confirm the study is well controlled
  • Work closely with the investigative sites to ensure understanding of laboratory procedures, study supply availability/accountability and the correct distribution of samples
  • Assist in the development of clinical operations SOPs
  • Other duties as assigned

Experience and Skills Desired:
  • BS/BA degree required in science/health-related field.
  • 1-3 years of experience in a relevant field supporting clinical trials through a clinical site, CRO or trial sponsor, clinical research coordinator
  • Ability to travel 25%-50% of the time during peak periods
  • Understanding and application of GCP, ICH, and applicable regulatory standards governing clinical research
  • Excellent written and oral communication and presentation skills
  • The ability to manage multiple priorities, while maintaining attention to detail is critical.
  • Ability to prioritize tasks and resources, meet deadlines, and be flexible to changing priorities.
  • Excellent computer skills (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook, and IXRS/EDC platforms)

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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