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Project Manager Biotech Jobs in New Port Richey, FL

Packaging Operator III

Tampa, FL · On-site

$18 - $20/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Report any observations to QA, Team Lead, Equipment Specialist, CPS Project Coordinator, or Manager ...

Maintain the proper chain of custody for all samples, managing aliquoting, storage, receipt, and ... projects for pharmaceutical and biotech clients, contributing expertise and innovative solutions.

Maintain the proper chain of custody for all samples, managing aliquoting, storage, receipt, and ... projects for pharmaceutical and biotech clients, contributing expertise and innovative solutions.

Take ownership of projects, ensuring their successful planning, budgeting, execution, and ... Mathematics, Biotechnology preferred - Prior consulting or advisory firm experience preferred ...

TekWissen group is a workforce management provider throughout the USA and many other countries in ... Our client is a leading biotechnology company that combines technological expertise with world ...

... biotechnology, or healthcare organization. * SAP Delivery Track Record: Proven success leading at ... Professional Project Management certification (e.g., PRINCE2, IPMA, or PMP) is highly preferred.

... biotechnology, or healthcare organization. * SAP Delivery Track Record: Proven success leading at ... Professional Project Management certification (e.g., PRINCE2, IPMA, or PMP) is highly preferred.

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... This role will also support Domestic tax matters and special projects as needed. The ideal ...

Showing results 21-40

Project Manager Biotech information

See New Port Richey, FL salary details

$19

$41

$68

How much do project manager biotech jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for project manager biotech in New Port Richey, FL is $41.19, according to ZipRecruiter salary data. Most workers in this role earn between $35.77 and $45.19 per hour, depending on experience, location, and employer.

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.

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 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.
What are popular job titles related to Project Manager Biotech jobs in New Port Richey, FL? For Project Manager Biotech jobs in New Port Richey, FL, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in New Port Richey, FL look for? The top searched job categories for Project Manager Biotech jobs in New Port Richey, FL are:
What cities near New Port Richey, FL are hiring for Project Manager Biotech jobs? Cities near New Port Richey, FL with the most Project Manager Biotech job openings:
Infographic showing various Project Manager Biotech job openings in New Port Richey, FL as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $85,670 per year, or $41.2 per hour.

Packaging Operator III

TekWissen LLC

Tampa, FL • On-site

$18 - $20/hr

Contractor

Re-posted 6 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:        Packaging Operator III 
Location:        Tampa, FL, 33634 
Duration:        12 Months    
Job Type:        Tempporary Assignment
Work Type:    Onsite 
Shift:               Monday to Friday from 07:00 AM to 03:30 PM
  
 
Summary
  • Execute assembly instructions per Batch Record requirements for Packaging and Labeling processes in compliance with cGMP guidelines.
  • This will require on-time and neat documentation during the execution to assure compliance.
  • Provide support to the Manufacturing Group, QA, Warehouse, and Facility operations by complying with company and FDA cGMP requirements.
  • Responsible for the performance of cleaning of Primary and Secondary Packaging rooms and Packaging equipment.
  • This will include the corresponding Room Sanitizations per Department's procedures.
Responsibilities
  • Follow batch record instructions in the execution of manual processes for Primary and Secondary Packaging as applicable.
  • Assist in the operation and set-up of automated equipment in the performance of certain primary or secondary packaging operations.
  • Assist in the reconciliation and movement (Chain of Custody) of materials between packaging areas and the warehouse.
  • Report any observations to QA, Team Lead, Equipment Specialist, CPS Project Coordinator, or Manager of potential issues that could result in deviation or investigation.
  • Perform Cleaning and Sanitization of Primary and Secondary Packaging rooms.
  • Support the Equipment Specialist in the execution of qualification protocols for new equipment as assigned.
  • Training on SOPs to remain current for job requirements, logbook entries, and GMP documentation.
  • Attend applicable meetings, discussions, etc., in support of these projects to meet the Production Schedule.
  • Participate in safety processes and meetings as applicable.
  • Maintain a positive, professional, and confidential relationship with sponsors.
  • Comply with all state and federal regulatory requirements and guidelines.
  • Other applicable duties as assigned.
  • Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear.
  • Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible.
  • Stop work where deemed necessary to maintain safety.
  • Operate and tend machines that perform one or more packaging functions, such as filling, marking, labeling, tying, packing, or wrapping containers.
Required Skills
  • 1–3 years of experience in packaging operations.
  • Experience in following batch record instructions and SOPs.
  • Supporting qualification protocols for new equipment.
  • Experience operating or assisting with automated packaging equipment.
  • Ability to perform cleaning and sanitization per procedure.
  • Familiarity with cGMP guidelines and FDA compliance.
  • Capable of assisting in reconciliation and movement of materials.
  • Proficiency in executing job documentation and logbook entries.
  • Participation in safety and sustainability processes.
  • Ability to report and escalate deviations or quality concerns.
  • Willingness to stop work to maintain safety when necessary.
  • Ability to attend and contribute to cross-functional meetings.
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

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