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Biotechnology Project Manager Jobs in Clover, SC

Zifo

GxP Lab Computing Analyst

Charlotte, NC

Manage lab computing aspects of installing new, retirement and relocation of equipment * Implement ... Ability to identify, track and complete tasks for multiple projects * Knowledge of laboratory ...

Zifo

GxP Lab Computing Analyst

Charlotte, NC · On-site

$70 - $100/hr

Manage lab computing aspects of installing new, retirement and relocation of equipment * Implement ... Ability to identify, track and complete tasks for multiple projects * Knowledge of laboratory ...

Zifo

GxP Lab Computing Analyst

Charlotte, NC · On-site

Manage lab computing aspects of installing new, retirement and relocation of equipment * Implement ... Ability to identify, track and complete tasks for multiple projects * Knowledge of laboratory ...

Zifo

GxP Lab Computing Analyst

Charlotte, NC · On-site

Manage lab computing aspects of installing new, retirement and relocation of equipment * Implement ... Ability to identify, track and complete tasks for multiple projects * Knowledge of laboratory ...

Amazon

Operations Manager

Charlotte, NC · On-site

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Re:Build Manufacturing

EHS Manager

Rock Hill, SC · On-site

$68K - $93K/yr

Our constantly evolving portfolio of projects includes parts and assemblies for clients in the ... pharma, biotech, clean tech, chemicals, energy, lifestyle, food production, and industrial ...

Re:Build Manufacturing

EHS Manager

Rock Hill, SC · On-site

$68K - $93K/yr

Our constantly evolving portfolio of projects includes parts and assemblies for clients in the ... pharma, biotech, clean tech, chemicals, energy, lifestyle, food production, and industrial ...

North Star Staffing Solutions

Auditor

Charlotte, NC · On-site

... Biotech and Pharmaceutical, Automotive, Construction, Engineering, Healthcare, Hospitality, Legal ... The Senior Auditor should be prepared to participate is different projects simultaneously while ...

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All JobsBiotechnology Project JobsBiotechnology Project Manager JobsBiotechnology Project Manager Jobs in Clover, SC

Biotechnology Project Manager information

See Clover, SC salary details

$18

$39

$65

How much do biotechnology project manager jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for biotechnology project manager in Clover, SC is $39.67, according to ZipRecruiter salary data. Most workers in this role earn between $34.42 and $43.51 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 job categories do people searching Biotechnology Project Manager jobs in Clover, SC look for?

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

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

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

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Clover, SC as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $82,514 per year, or $39.7 per hour.

Senior Metrology or Calibration Engineer (Contract)

VTI Life Sciences

Charlotte, NC • On-site

Contractor

Posted 21 days ago

Job description

Location: Onsite for initial project Audit/GAP Analysis and Remote for summary reports with periodic on-site travel (as required).
Duration: Approximately 6 weeks (potential for extension)
Client: Confidential Pharmaceutical / Medical Device Company
Position Summary
VTI Life Sciences is seeking an experienced Senior Metrology or Calibration Specialist to support a comprehensive Quality Control (QC) and Equipment Metrology Program assessment for a regulated pharmaceutical and medical device manufacturing facility. The successful candidate will evaluate the overall health of the metrology program by validating approximately 600 metrology assets and associated records, identifying compliance gaps, assessing instrument performance risks, and recommending improvements to strengthen regulatory compliance and audit readiness.
In addition to the assessment, the candidate will provide technical support for equipment decommissioning, installation, calibration, and integration of critical laboratory and manufacturing equipment into the site's metrology program.
Key Responsibilities
  • Perform a comprehensive assessment of the site's Metrology Program.
  • Review and validate approximately 600 metrology assets, including laboratory instruments, timers, thermometers, balances, gauges, pressure and temperature devices, and other calibrated equipment.
  • Evaluate calibration records, maintenance history, asset identification, calibration intervals, traceability, and documentation for compliance with GMP and internal procedures.
  • Assess metrology program effectiveness, identify gaps, and recommend corrective and preventive actions (CAPAs).
  • Evaluate known instrument performance risks and recommend improvements to increase equipment reliability and audit readiness.
  • Support equipment decommissioning activities, ensuring proper documentation, asset disposition, and quality system compliance.
  • Provide technical oversight for installation, calibration, and commissioning support of critical laboratory and process equipment.
  • Review calibration procedures and recommend improvements where appropriate.
  • Verify traceability to NIST (or equivalent national standards), uncertainty considerations, and calibration best practices.
  • Prepare detailed assessment reports, observations, risk assessments, and executive summaries.
  • Collaborate with Quality Assurance, Engineering, Validation, Manufacturing, and Laboratory personnel to resolve metrology issues.
  • Support regulatory inspection readiness and internal audit preparation.
Required Qualifications
  • Bachelor's or Associate  (certification) degree in Engineering, Physics, Metrology, Instrumentation, Engineering Technology, or a related scientific discipline.
  • Minimum 7 years of metrology, calibration, or instrumentation experience in FDA-regulated pharmaceutical, biotechnology, medical device, or life sciences industries.
  • Extensive knowledge of GMP requirements and calibration program management.
  • Strong understanding of FDA 21 CFR Parts 210, 211, and 820 (QMSR), ISO 13485, ISO/IEC 17025, and applicable industry standards.
  • Experience assessing large calibration programs involving hundreds of assets.
  • Plus if experience with computerized calibration management systems (e.g., Blue Mountain RAM, Beamex CMX, IndySoft, GAGEtrak, Maximo, SAP PM, or equivalent).
  • Strong understanding of calibration uncertainty, traceability, and measurement science.
  • Excellent technical writing, documentation, and communication skills.
Preferred Qualifications
  • ASQ Certified Calibration Technician (CCT) or equivalent certification.
  • Experience supporting FDA inspections and regulatory audits.
  • Experience performing gap assessments and remediation projects.
  • Familiarity with commissioning, qualification (IQ/OQ/PQ), and equipment lifecycle management.
  • Experience with laboratory and manufacturing instrumentation in pharmaceutical or medical device facilities.
Deliverables
  • Comprehensive QC Metrology Program Assessment Report.
  • Asset-by-asset validation summary and compliance review.
  • Gap assessment with risk ranking and recommended corrective actions.
  • Equipment decommissioning documentation support.
  • Installation and calibration support for critical equipment.
  • Executive summary with prioritized recommendations to improve compliance, reliability, and audit readiness.
Desired Skills
  • Strong analytical and problem-solving abilities.
  • Excellent organizational and project management skills.
  • Ability to work independently with minimal supervision.
  • Strong interpersonal skills with the ability to communicate effectively with cross-functional teams and client stakeholders.
  • Ability to prioritize multiple tasks while meeting aggressive project timelines.

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