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Biotechnology Project Manager Jobs in Holly Ridge, NC

Biotechnology Project Manager information

See Holly Ridge, NC salary details

$16

$35

$59

How much do biotechnology project manager jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for biotechnology project manager in Holly Ridge, NC is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $31.20 and $39.38 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 Holly Ridge, NC?

For Biotechnology Project Manager jobs in Holly Ridge, NC, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Holly Ridge, NC look for?

The top searched job categories for Biotechnology Project Manager jobs in Holly Ridge, NC are:

What cities near Holly Ridge, NC are hiring for Biotechnology Project Manager jobs?

Cities near Holly Ridge, NC with the most Biotechnology Project Manager job openings:

Quality Manager (Regulated Industry)

Mentor Technical Group

Jacksonville, NC • On-site

Full-time

Posted 4 days ago


Job description

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
 

ESSENTIAL FUNCTIONS: (List specific duties and responsibilities)

  1. Ensures the creation, revision, and enforcement of all aspects of MENTOR and the assigned client facilities Quality Management System (QMS), or in situations where MENTOR operates within the client's QMS, facilitates the integration and ongoing oversight aspects required by that QMS.
  2. Lead the events & root cause analysis processes.
  3. Oversight of the training programs and lead the inspection readiness programs, and vendor management programs.
  4. Lead the review and administration of quality service level agreement (SLA) and Quality Management Systems as it pertains to quality and compliance requirements.
  5. Also, will be responsible for the development and implementation of a strategy to ensure the client requirements are met
  6. Will travel to support MTG clients and operations as required

EDUCATIONAL or EQUIVALENT REQUIREMENTS: (Minimum required to perform the job)

  1. Bachelor's degree is required; Sciences or Engineering is preferred.
  2. Minimum of five (5) years professional experience in compliance, quality systems and/or internal auditing within the regulated industry.
  3. Previous experience leading teams or projects.
  4. Requires strong technical writing skills (English and Spanish).
  5. Ability to effectively read, write and verbally communicate in English and Spanish.
  6. Computer literacy with MS Office applications (Word, Excel, Power Point, Outlook) and Quality Management Systems (e.g. Trackwise).
  7. Above average organizing, analyzing and a minimum of math (practical application of fractions, percentages, ratios, proportions, basic algebra) to determine organizational, Customer and regulatory problems and formulate corrective action plans.
  8. Ability to adapt to changing responsibilities.
  9. Requires effective interpersonal skills as demonstrated through prior experience.
  10. Ability to work independently under minimal guidelines and supervision.
  11. Working knowledge of applicable regulations and standards, including, but not limited to, GMP, GDP regulations and ISO standards.
  12. Ability to motivate, train and develop staff within the MENTOR’s team.
  13. Willingness to demonstrate through daily activities a model of continuous monitoring of quality system activities to ensure compliance with documented standards.
  14. Demonstrated ability to analyze data and performance metrics.
  15. Demonstrate decision making capabilities.

RESPONSABILITIES:

  1. Responsible for establishing objectives, mentoring direct and reports and managing resources to ensure successful execution of the Quality Management System.
  2. Provide support for design, execution and maintenance of quality system processes at respective departments.
  3. Help department to coordinate training to operating procedure changes or new system implementation.
  4. Recommend, implement and direct others to modify operational methods and practices along with overall strategy to enhance department effectiveness.
  5. Lead the implementation and maintenance of quality systems, including data analysis to identify opportunities for quality system improvement.
  6. Maintain independence and oversight for clients documentation review and approval.
  7. Reviews and approves protocols and final reports; escalate deviations from performance standards to their management.
  8. Monitors and manages clients CAPA’s non-conformances and customer complaints.
  9. Managed writing and review operating procedures (OP’s) to ensure compliance, efficiency and clarity.
  10. Writing and reviewing quality system work instructions.
  11. Responsible for conducting and/or supporting audit finding investigations including but not limited to mitigation, corrective action(s) and preventive action(s) where applicable. Collaborate with department managers to develop and implement sustainable remediation action plans.
  12. Leads continuous improvement projects for multiple sites.
  13. Actively participates in assigned quality facilities projects.
  14. Implement quality compliance processes (i.e. work instructions) and other harmonization processes at multiple sites.
  15. Act as a point of contact for customers, suppliers, and internal employees regarding all contracts and compliance requests.
  16. Work with all necessary internal departments to ensure compliance requirements are achieved as related to industry and customer expectations based on customer driven goals.
  17. Management of all regulatory aspects including external and internal audits, investigations, and corrective/preventive actions.
  18. Ensure the adherence of our employees to the standard operating procedures (SOPs) established by the clients.
  19. Manage an internal audit process to assure the adherence of the client SOPs 20. Any other duties as required by Quality and Customer Services Director to support normal client’s operations


Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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