ZipRecruiter

Log In

1

Biotechnology Project Manager Jobs (NOW HIRING)

PSC Biotech

Project Manager

Allentown, PA

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Your Role The Project Manager will play a key role in the planning, oversight, and leading of cross ...

PackGene Biotech lnc

Project Manager

Houston, TX · On-site

Project Manager Site: Houston, TX Department: Project Management FLSA Status: Exempt Job Status ... Company Background PackGene Biotech was founded in 2014 by a team of visionary scientists united by ...

PACKGENE BIOTECH INC

Project Manager

Houston, TX

Project Manager Site: Houston, TX Department: Project Management FLSA Status: Exempt Job Status ... Company Background PackGene Biotech was founded in 2014 by a team of visionary scientists united by ...

Actalent

Project Manager

San Diego, CA · On-site

$38.46/hr

Lead and manage projects within the biotech and pharmaceutical industries. * Ensure successful project delivery from initiation to completion. * Utilize project management tools such as MS Project to ...

DPS Group

Project Manager

Conshohocken, PA · On-site

The successful candidate must have a strong design discipline background along with experience managing architectural and engineering/design projects in the biotech and/or pharmaceutical industries.

next page

Showing results 1-20

People also search for

All JobsBiotechnology Project JobsBiotechnology Project Manager Jobs

Biotechnology Project Manager information

See salary details

$21

$46

$76

How much do biotechnology project manager jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for biotechnology project manager in the United States is $46.24, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $50.72 per hour, depending on experience, location, and employer.

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 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 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.

More about Biotechnology Project Manager jobs
What cities are hiring for Biotechnology Project Manager jobs? Cities with the most Biotechnology Project Manager job openings:
What states have the most Biotechnology Project Manager jobs? States with the most job openings for Biotechnology Project Manager jobs include:
What job categories do people searching Biotechnology Project Manager jobs look for? The top searched job categories for Biotechnology Project Manager jobs are:
Biotechnology Project Manager jobs near you
Shutdown Project Manager (Pharma/Biotech)

Shutdown Project Manager (Pharma/Biotech)

Cybercoders

Thousand Oaks, CA

$150K - $240K/yr

Full-time

Posted 2 days ago

Job description

Shutdown Project Manager (Pharma/Biotech)

Shutdown Project Manager (Pharma/Biotech)
Location: Thousand Oaks, CA
Salary: $150K-$240K base (salary depends on experience) 
Position Overview
Lead and own planned shutdowns, turnarounds, and critical maintenance projects for pharmaceutical and biotechnology facilities. The Shutdown Project Manager will plan, coordinate, and execute multi-disciplinary shutdown work to meet safety, regulatory (cGMP/FDA/EMA), and schedule objectives while managing budget, stakeholders, contractors, and validation activities to resume production on time and compliant.
Key Responsibilities

  • Plan and manage end-to-end shutdowns, turnarounds, and major maintenance windows in pharma/biotech facilities, ensuring on-time, on-budget and compliant execution.
  • Develop detailed shutdown schedules, phased work plans and resource loading using Primavera P6 and MS Project; integrate contractor, maintenance and validation activities.
  • Lead pre-shutdown planning including scope definition, risk assessments, procurement, materials staging, and readiness reviews.
  • Coordinate cross-functional teams (engineering, operations, quality, validation, EHS, facilities) and external contractors to align work packages and interfaces.
  • Manage Validation Master Plan activities during shutdowns: IQ/OQ/PQ sequencing, equipment requalification, and documentation to meet cGMP/FDA/EMA requirements.
  • Implement and enforce safety, isolation/tagout, and EHS requirements during all shutdown phases; lead pre-job briefings and lessons-learned.
  • Control project budgets, change orders and capital spending; prepare cost forecasts, track expenditures and justify contingency use.
  • Maintain strict change control, documentation, and regulatory traceability for all maintenance, modification and commissioning work.
  • Use PLC/SCADA knowledge where required to coordinate control system shutdown/bring-up procedures with automation teams.
  • Provide clear status reporting to senior stakeholders, prepare post-shutdown reports, drive continuous improvement and update shutdown playbooks.

Qualifications

  • Bachelors degree in Engineering, Construction Management, Life Sciences or related field required; advanced degree preferred.
  • Minimum 7 years project management experience with at least 3 full shutdown/turnaround cycles in pharmaceutical or biotech facilities.
  • Proven knowledge of life science manufacturing and cleanroom environments, including cGMP requirements and experience with FDA/EMA inspections or audits.
  • Strong schedule management experience with Primavera P6 and Microsoft Project; demonstrated ability to build, compress and recover complex schedules.
  • Experience managing Validation Master Plan activities and equipment requalification (IQ/OQ/PQ) during shutdowns.
  • Familiarity with PLC, SCADA, and industrial control system coordination during shutdown and restart activities.
  • Demonstrated ability to manage capital projects, contractors, and supply chain for mission-critical and clean room work.
  • Excellent stakeholder management, communication skills, and experience leading cross-functional teams under time pressure.
  • Preferred: experience across Laboratory, VMP, Data Center, Commercial, Industrial, Ground-Up/New Construction, Public Works, Educational, High Rise, Addition, Lab, Healthcare, Medical, Hospital, Pharmaceutical and Biotech projects.
  • Certifications preferred: PMP or equivalent project management certification; experience with Quality/Compliance certifications a plus.

Benefits

Full Benefits Included 

- For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. CyberCoders will consider for Employment in the City of Los Angeles qualified Applicants with Criminal Histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring (Ban the Box) Ordinance.This job was first posted by CyberCoders on 05/28/2026 and applications will be accepted on an ongoing basis until the position is filled or closed.Everforth CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. Our hiring process includes AI screening for keywords and minimum qualifications. Recruiters review all results.  Everforth CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. Everforth CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at Benefits@CyberCoders.com to make arrangements.
CyberCoders logo

About CyberCoders

Sourced by ZipRecruiter

CyberCoders is a cutting-edge recruiting firm headquartered in Irvine, CA, US. The company operates within the technology industry, specializing in connecting talented professionals with suitable positions across a variety of sectors. Offering a broad spectrum of services, CyberCoders uses innovative, data-driven strategies and a proprietary matching technology to pair candidates with suitable job openings. Since its inception in 1999, CyberCoders has distinguished itself as an industry trailblazer. The company's mission is to deliver effective talent solutions, thus enabling both businesses and workers to achieve their goals.

Industry

Technology, communication and media

Company size

51 - 200 Employees

Headquarters location

Irvine, CA, US

Year founded

1999

Social media

FacebookTwitter

View All CyberCoders Jobs