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Biotechnology Project Manager Jobs in Columbia, SC

Spirax Sarco

Project Drafting Designer

Blythewood, SC · On-site

Manages special projects as needed and requested. * Serves as technical support for customers and ... Biotechnology, Power Generation, Semiconductors, and Healthcare. With a presence in 165 countries ...

Amgen

Imaging Specialist Manager

Columbia, SC · On-site +1

It is key to our becoming one of the world's leading biotechnology companies. We are global ... Project and Program management and phenomenal communication skills * Degree educated THRIVE What ...

Amgen

Strategic Sourcing Manager

Columbia, SC

$119K - $154K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

Spirax-Sarco Ltd.

Operations Manager

Blythewood, SC

Align cross-functional stakeholders to execute strategic priorities, projects, and resource plans ... Biotechnology, Power Generation, Semiconductors, Healthcare, and many others. With a presence in ...

New

ImpactBio

Human Resource Coordinator

Columbia, SC · On-site

$17.25 - $22.50/hr

Communicate with employees, managers, and internal stakeholders regarding onboarding status ... Participate in HR projects and process improvement initiatives designed to enhance the employee ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for biotechnology project manager in Columbia, SC is $42.78, according to ZipRecruiter salary data. Most workers in this role earn between $37.12 and $46.92 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

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

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Biotechnology Project Manager jobs in Columbia, SC?

For Biotechnology Project Manager jobs in Columbia, SC, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Columbia, SC look for?

The top searched job categories for Biotechnology Project Manager jobs in Columbia, SC are:

What cities near Columbia, SC are hiring for Biotechnology Project Manager jobs?

Cities near Columbia, SC with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Columbia, SC 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 $78,539 per year, or $37.8 per hour.

Senior Project Manager

THE RITEDOSE CORPORATION

Columbia, SC • On-site

Full-time

Posted 3 days ago

New

Job description

The Senior Project Manager leads the technical and commercial execution of multiple client programs for sterile, unit-dose products manufactured by Blow-Fill-Seal (BFS) aseptic processing — from feasibility and technology transfer through registration batches, process validation, launch, and ongoing commercial supply. This customer- facing role is the primary point of contact for assigned clients and directs cross-functional teams across the site. It is the senior individual-contributor role within the Project Management Office and is positioned as a development role for progression into Project Management leadership: the incumbent is expected to mentor project managers, act as designee for the Director of Project Management, and take an increasing share of portfolio-level and PMO governance responsibility.

Key Responsibilities:
  • Lead assigned client programs end to end for sterile BFS products — feasibility, quotation support, technology transfer, engineering and registration/exhibit batches, process validation (PPQ), stability, launch, and commercial supply.
  • Serve as the primary customer contact and own the relationship at both working and executive level, including project review meetings, business reviews, and joint steering committees.
  • Develop and maintain integrated project schedules, critical-path and resource analyses, risk registers, and milestone tracking tools. Report any variance as soon as it is recognized, together with a recovery plan.
  • Direct cross-functional teams — Product Development, Analytical Services, Quality, Operations, Engineering, Supply Chain, Regulatory Affairs, and Finance — without direct reporting authority.
  • Own project scope and change control: identify out-of-scope work, develop and negotiate change orders, and support quoting, revenue forecasting, and cash-flow phasing with Finance.
  • Coordinate regulatory deliverables with Regulatory Affairs in support of ANDA, NDA/505(b)(2), and post-approval submissions, including customer data packages and response timelines.
  • Represent Project Management in customer audits, technical visits, and regulatory inspections;  coordinate cross-functional responses to customer technical queries and audit observations.
  • Mentor and provide day-to-day direction to Project Managers, Associate Project Managers, and Project Coordinators, including review of their project plans and customer-facing deliverables.
  • Serve as designee for the Director of Project Management as assigned, including portfolio reporting to site leadership and representation in leadership and governance meetings.
  • Advance PMO capability — stage-gate standards, templates, project KPIs and dashboards, and lessons- learned reviews at program close.
  • Establish and maintain internal and external meeting agendas and minutes as the controlled record of project decisions.
Qualifications:
  • Bachelor's degree in Life Sciences, Chemistry, Engineering, Pharmacy, or a related field.
  • Minimum 5-7 years of pharmaceutical, biotech, or CDMO experience, including at least 3 years directly managing projects.
  • Sterile/aseptic manufacturing experience is preferred. Blow-Fill-Seal, sterile injectable, ophthalmic, or inhalation unit-dose experience is strongly preferred.
  • Demonstrated ownership of at least one product through technology transfer and process validation into commercial supply.
  • Direct external customer-facing experience in a contract development and manufacturing environment.
  • Working knowledge of cGMP (21 CFR 210/211), FDA, EMA, ICH, and EU GMP Annex 1 requirements.
  • PMP certification preferred; Lean Six Sigma a plus.
  • Experience mentoring or leading project managers, or demonstrated readiness to progress into a people- leadership role.
Required Skills & Competencies:
  • Strong customer relationship management, including the ability to hold a defensible technical positionwith a client while protecting the relationship.
  • Excellent written and verbal communication; able to present credibly to both customer and Ritedose executive leadership.
  • Financial fluency - project budgets, change orders, capital versus expense, and the revenue impact ofschedule movement.
  • Technical judgment in aseptic processing, validation, and analytical/stability requirements sufficient to challenge and defend proposed timelines.
  • Proficiency with project scheduling tools (MS Project, Smartsheet, or equivalent) and with electronic QMSand ERP systems.
  • Leadership presence and the ability to influence without authority across a matrixed organization.
  • Discretion in handling confidential customer information and competing client interests.
Work Environment & Physical Requirements:
  • On-site position in Columbia, SC, with regular presence required in manufacturing and laboratory areas.
  • Must be able to gown for and enter classified/controlled areas and comply with GMP dress code and site EHS requirements.
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About Ritedose

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Industry

Pharmaceutical and medicine manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Columbia, SC, US

Year founded

1995

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