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Project Manager Biotech Jobs in Lancaster, PA (NOW HIRING)

Higher levels assume increasing responsibility for project leadership, investigations, method ... Ability to manage multiple priorities and work effectively in a team environment. Demonstrated ...

Microbiologist

York, PA · On-site

$70K - $80K/yr

Higher levels assume increasing responsibility for project leadership, investigations, method ... Bachelor's degree in Microbiology, Biology, Biotechnology, Biochemistry, or a related scientific ...

Higher levels assume increasing responsibility for project leadership, investigations, method ... Bachelor's degree in Microbiology, Biology, Biotechnology, Biochemistry, or a related scientific ...

Engineering Intern

York, PA · On-site

$16 - $18/hr

... utility-related projects in a regulated biotech manufacturing environment. * Assist with ... Ability to work independently and manage multiple tasks effectively. * Detail-oriented with a ...

Engineering Intern

York, PA · On-site

$16.50 - $21.50/hr

... utility-related projects in a regulated biotech manufacturing environment. * Assist with ... Ability to work independently and manage multiple tasks effectively. * Detail-oriented with a ...

Engineering Intern

York, PA

$16.50 - $21.50/hr

... utility-related projects in a regulated biotech manufacturing environment. Assist with ... Ability to work independently and manage multiple tasks effectively. Detail-oriented with a ...

Utilization should be detailed enough to reflect the cost per project (for client) and costs ... Experience in an FDA regulated Biotech/Pharmaceutical industry * Experience in working in an FTE ...

The role includes project management responsibilities for selected customer programs and strategic ... Hybrid Leadership & Strategic Execution - Communicates effectively across PSC Biotech and ...

The role includes project management responsibilities for selected customer programs and strategic ... Hybrid Leadership & Strategic Execution - Communicates effectively across PSC Biotech and ...

Senior Director of Quality

York, PA · On-site

$150K - $200K/yr

The role includes project management responsibilities for selected customer programs and strategic ... Hybrid Leadership & Strategic Execution - Communicates effectively across PSC Biotech and ...

Packaging Engineer

Lancaster, PA · On-site +1

$70K - $110K/yr

Strong problem-solving, analytical, and project management skills * Excellent written and verbal ... Experience in pharmaceutical, medical device, biotech, consumer products, food & beverage, or ...

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Project Manager Biotech information

See Lancaster, PA salary details

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$44

$74

How much do project manager biotech jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for project manager biotech in Lancaster, PA is $44.94, according to ZipRecruiter salary data. Most workers in this role earn between $38.99 and $49.28 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What are popular job titles related to Project Manager Biotech jobs in Lancaster, PA?

For Project Manager Biotech jobs in Lancaster, PA, the most frequently searched job titles are:

What cities near Lancaster, PA are hiring for Project Manager Biotech jobs?

Cities near Lancaster, PA with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Lancaster, PA as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $93,476 per year, or $44.9 per hour.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill-finish services. From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team's expertise to create a process design for our clients' products that best suits their needs.

The Experience With operations spanning the globe and featuring a multi-cultural team, BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers.

As such, you will not only be offered a compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn. At BioTechnique, it's about more than just a job-it's about your career and your future. Your Role The Microbiologist performs microbiological testing, environmental monitoring (EM), detection, enumeration, and testing (DET) activities to support manufacturing operations and product quality within a GMP-regulated environment.

This role is responsible for executing laboratory testing, supporting validation activities, maintaining data integrity, and ensuring compliance with cGMP, regulatory, and company quality requirements. Higher levels assume increasing responsibility for project leadership, investigations, method validations, and mentoring junior staff. Perform microbiological testing, sampling, and laboratory analyses in accordance with approved SOPs.

Execute Environmental Monitoring (EM) activities, including viable and non-viable air, surface, and personnel monitoring. Perform Disinfectant Efficacy Testing (DET). Experience with bioburden, endotoxin, and related microbiological assays on client samples.

Set up, operate, and maintain laboratory equipment and instrumentation. Perform and document method validations, qualifications, and trend analyses. Review, analyze, and accurately document testing results while maintaining data integrity.

Report and participate in investigations related to OOS, OOT, and atypical results. Support contamination control, GMP compliance, and laboratory continuous improvement initiatives. Author, review, and execute protocols, reports, and technical documentation.

Train, mentor, and provide technical guidance to junior microbiologists and laboratory personnel. Lead complex testing, validation, and laboratory projects. Follow all safety procedures and wear required PPE.

Requirements Bachelor's degree in Microbiology, Biology, Biotechnology, Biochemistry, or a related scientific discipline 4-6 years experience of Quality Control Microbiology experience within a regulated pharmaceutical, biotechnology, or related industry. Knowledge of microbiological testing methods, environmental monitoring programs, and contamination control principles. Understanding of cGMP regulations, data integrity requirements, and laboratory documentation practices.

Experience with method validation, investigations, and trend analysis preferred. Strong analytical, problem-solving, organizational, and communication skills. Ability to manage multiple priorities and work effectively in a team environment.

Demonstrated leadership and mentoring capabilities for advanced-level positions. Experience with LIMS, eQMS, or laboratory data systems is preferred. Must be authorized to work in the U.S

No C2C at this time. Benefits Offering a full suite of benefits, PSC Biotech is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.

Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more. 401(k) and 401(k) matching PTO, Sick Time, and Paid Holidays Education Assistance Pet Insurance Fitness Benefits (Membership discounts and other perks/services at qualifying gyms like Anytime Fitness, 24-Hour Fitness, and more) Financial Perks and Discounts Equal Opportunity Employment Statement PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination.

Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant's, employee's, or intern's actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law. #LI-RW1.