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Biotechnology Project Manager Jobs in Spring, TX

GlobalPundits

Mechanical Design Engineer

Houston, TX

$72.50K - $98.30K/yr

... disciplines, project management, vendors, and clients Execute work in compliance with Project ... biotechnology Intermediate knowledge of: Equipment specification development Instrumentation and ...

Delan Associates, Inc

Mechanical Design Engineer

Houston, TX

$72.60K - $98.40K/yr

... project management, vendors, and clients Execute work in compliance with Project Quality Plan and ... biotechnology Intermediate knowledge of: o Equipment specification development o Instrumentation ...

Delan Associates, Inc

Mechanical Design Engineer

Houston, TX · On-site

$72.60K - $98.40K/yr

... project management, vendors, and clients Execute work in compliance with Project Quality Plan and ... biotechnology Intermediate knowledge of: o Equipment specification development o Instrumentation ...

Deloitte

Patience Services Technical Manager

Houston, TX

$110.80K - $111.30K/yr

Leveraging your expertise in patient services, you will interface between pharmaceutical, biotech ... You will design, implement and optimize patient support programs, define project roadmaps and ...

Lonza

Associate Director, Engineering

Houston, TX · On-site

... biotechnology, or similarly regulated manufacturing environments. * Proven ability to lead complex capital projects, manage significant CapEx budgets, and deliver results in a GMP context. * Strong ...

Lonza

Associate Director, Engineering

Houston, TX · On-site

... biotechnology, or similarly regulated manufacturing environments. * Proven ability to lead complex capital projects, manage significant CapEx budgets, and deliver results in a GMP context. * Strong ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of May 30, 2026, the average hourly pay for biotechnology project manager in Spring, TX is $41.15, according to ZipRecruiter salary data. Most workers in this role earn between $35.72 and $45.14 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.

What are popular job titles related to Biotechnology Project Manager jobs in Spring, TX? For Biotechnology Project Manager jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Spring, TX look for? The top searched job categories for Biotechnology Project Manager jobs in Spring, TX are:
What cities near Spring, TX are hiring for Biotechnology Project Manager jobs? Cities near Spring, TX with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Manufacturing Deviation Investigator

Manufacturing Deviation Investigator

TekWissen LLC

Houston, TX • On-site

$20 - $24/wk

Contractor

Posted 28 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:       Manufacturing Deviation Investigator / Sr. Quality Records Investigator
Location:       Houston, TX - 77047
Duration:       6 Months    
Job Type:       Contract    
Work Type:   Onsite 
 Shift:             Monday to Friday - 08:00 AM to 05:00 PM
 
 
Summary
 
The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.
 
 
Responsibilities
  • Technical writing for the educated but uninformed reader, translate difficult and complex scientific events into a brief and cohesive report as a finished product.
  • Accurately capture immediate actions and containment of the event, address comments from both internal and external clients on the compiled final report.
  • Gathering Data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation, assessment of event for impact to Safety Identity Strength Quality Purity (SISQP), perform trending analysis, identification of Corrective and Preventative Actions to reduce deviation recurrence, performance of Risk Assessments, Causing Mapping, Interviewing.
  • Management of multiple projects and timelines concurrently.
  • Ability to adhere to standard timeline, and escalate actions appropriately for resolution in a timely manner.
  • Participation in the Daily Management meetings to update leadership or current deviation statuses.
  • Routine interaction with the customer, including compilation of Power Points to communicate investigational current status, Alignment meetings, facilitated reviews, CAPA discussions, Comments resolution.
  • Work on the manufacturing floor for data gathering, observing of processes for investigations, and performance of associate interviews.
  • Meeting Facilitation and participation, aligning internal review team and area subject matter experts on an agreed to investigational path forward.
  • Complex Conflict resolution, problem solving in a cross functional setting, and ability to keep the meeting on track to achieve objectives of varying difficulty.
  • Attendance and occasional leadership of the daily management system and participating/leading the deviation review board.
  • Perform other duties as assigned. 
Required Skills 
  • Prior experience in Technical writing and documentation
  • Prior experience in performing in Deviation investigation and root cause analysis (RCA)
  • Strong hands on experience with CAPA (Corrective and Preventive Actions) creation and follow-through
  • Understanding of cGMP and pharmaceutical/biotech manufacturing
  • Quality systems and deviation lifecycle management
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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