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Project Manager Cdmo Jobs in Pennsylvania (NOW HIRING)

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... Collaborate with scientists, project teams, management, Business Development, and clients to ...

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... Collaborate with scientists, project teams, management, Business Development, and clients to ...

Mechanical Engineer

Tyrone, PA · On-site

$83K - $114K/yr

Support capital and expense projects related to equipment upgrades, replacements, and reliability ... Manage contractors and vendors, including scope development, execution oversight, and safety ...

Material Handler, Packaging

Philadelphia, PA · On-site

$17 - $20.50/hr

... CDMO) with locations across North America and Italy. We offer a wide range of manufacturing ... project management, human resources, and environmental health and safety. Our benefits package is ...

Material Handler, Packaging

Philadelphia, PA · On-site

$17 - $20.50/hr

... CDMO) with locations across North America and Italy. We offer a wide range of manufacturing ... project management, human resources, and environmental health and safety. Our benefits package is ...

Packaging Operator

Philadelphia, PA · On-site

$17.25 - $20.75/hr

... CDMO) with locations across North America and Italy. We offer a wide range of manufacturing ... project management, human resources, and environmental health and safety. Position Packaging ...

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... If you're looking for an opportunity to combine technical expertise, project management, and ...

Support capital and expense projects related to equipment upgrades, replacements, and reliability ... Manage contractors and vendors, including scope development, execution oversight, and safety ...

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... If you're looking for an opportunity to combine technical expertise, project management, and ...

Showing results 21-40

Project Manager Cdmo information

What is a project manager CDMO?

A Project Manager CDMO (Contract Development and Manufacturing Organization) is responsible for overseeing pharmaceutical or biotech projects outsourced to CDMOs. They coordinate between clients and internal teams to ensure timely delivery, quality, and compliance with regulatory standards. Their role includes managing project timelines, budgets, and resources, as well as communicating progress and addressing issues that may arise during drug development and manufacturing processes.

How does a project manager at a CDMO typically coordinate between clients and internal teams throughout a project lifecycle?

A Project Manager at a Contract Development and Manufacturing Organization (CDMO) acts as the central point of contact for clients and internal teams, ensuring clear communication and alignment of project goals. They regularly facilitate meetings, track project milestones, and proactively address potential issues or changes in scope. This involves close collaboration with departments such as R&D, manufacturing, quality assurance, and regulatory affairs to meet client expectations and project timelines. Effective project managers also document progress and maintain transparent reporting to both clients and internal stakeholders.

What are the key skills and qualifications needed to thrive as a project manager in a CDMO, and why are they important?

To excel as a Project Manager in a CDMO, you need a strong background in project management, life sciences, and regulatory compliance, often supported by a relevant degree and PMP certification. Familiarity with project management software (like MS Project or Smartsheet), quality management systems, and industry-specific regulations such as GMP are typically required. Outstanding organizational, communication, and stakeholder management skills help you effectively coordinate cross-functional teams and client expectations. These competencies are vital for delivering complex projects on time and within budget while maintaining regulatory standards and client satisfaction.

What are popular job titles related to Project Manager Cdmo jobs in Pennsylvania?

For Project Manager Cdmo jobs in Pennsylvania, the most frequently searched job titles are:

What cities in Pennsylvania are hiring for Project Manager Cdmo jobs?

Cities in Pennsylvania with the most Project Manager Cdmo job openings:

Infographic showing various Project Manager Cdmo job openings in Pennsylvania as of August 2026, with employment types broken down into 84% Full Time, 14% Part Time, 1% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Scientist III, Process Chemistry

Abzena Inc.

Bristol, PA • On-site

Full-time

Re-posted yesterday


Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
We are seeking a highly motivated Scientist III to join our Process Development team. The successful candidate will lead the development, optimization, and scale-up of synthetic processes for small molecules, linker-payloads, intermediates, and related compounds from early development through cGMP manufacturing. This role requires strong technical expertise, excellent problem-solving skills, and the ability to collaborate effectively with cross-functional teams.
Responsibilities
• Design, execute, and optimize synthetic routes for small molecules, intermediates, and complex drug-linker compounds.
• Develop scalable, robust, and cost-effective manufacturing processes suitable for pilot plant and cGMP production.
• Plan and perform laboratory experiments, analyze data, and interpret results to guide process improvements.
• Troubleshoot challenging synthetic and scale-up issues using sound scientific principles.
• Collaborate with Analytical Development, Manufacturing, MSAT, Quality, Supply Chain, and Project Management teams to ensure successful technology transfer and manufacturing campaigns.
• Prepare technical reports, batch records, process descriptions, risk assessments, and technology transfer documentation.
• Maintain accurate laboratory notebooks and ensure documentation complies with company and regulatory standards.
• Mentor junior scientists and provide technical guidance on experimental design and process development.
• Support client meetings by presenting technical data and project updates.
• Contribute to continuous improvement initiatives focused on safety, quality, efficiency, and sustainability
Qualifications
• Ph.D. in Organic Chemistry with 2+ years of industrial experience, or
• M.S. in Organic Chemistry with 5+ years of industrial experience, or
• Strong knowledge of synthetic organic chemistry and process development.
• Experience with reaction optimization, impurity control, and process scale-up.
• Experience with analytical techniques such as UPLC, HPLC, LC-MS, GC, and NMR.
• Excellent scientific writing, communication, and presentation skills.
• Demonstrated ability to manage multiple projects in a fast-paced environment.
Preferred
• Experience in pharmaceutical, biotechnology, or CDMO environments.
• Experience supporting cGMP manufacturing campaigns and technology transfer.
• Experience with linker-payload synthesis, peptide coupling chemistry, or highly potent compounds is desirable.
Physical Requirements
• Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time.
• Frequently lift and or move objects up to 30 pounds.
• Stand/walk during entire length of shift.
• Use arms, hands, and fingers to handle, feel or reach.
• Ability to climb, balance, stoop, kneel, crouch, or crawl.
• Visual abilities including near and far sight, color, peripheral vision, depth, and ability to focus.
• Ability to work with a PAPR and gown during work with high potent materials.
FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.