ZipRecruiter

Log In

1

Molecular Operations Director Jobs (NOW HIRING)

Lonza

Director, Operations

Walkersville, MD · On-site +1

$198K - $232K/yr

Director, Operations Location: This position is currently remote. A future transition to an on-site ... S. growth investment project supporting small molecule drug substance manufacturing. This role ...

Lonza

Director, Operations

Walkersville, MD · On-site +1

$198K - $232K/yr

Director, Operations Location: This position is currently remote. A future transition to an on-site ... S. growth investment project supporting small molecule drug substance manufacturing. This role ...

previous page

Showing results 41-60

All JobsHealthcare JobsMedical Research JobsClinical Research Manager JobsMolecular Operations Director Jobs

Molecular Operations Director information

See salary details

$34K

$107.7K

$179.5K

How much do molecular operations director jobs pay per year?

As of Sep 11, 2026, the average yearly pay for molecular operations director in the United States is $107,680.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $135,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Molecular Operations Director jobs?

For Molecular Operations Director jobs, the most frequently searched job titles are:

Infographic showing various Molecular Operations Director job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $107,680 per year, or $51.8 per hour.

Clinical Molecular Technologist

Chicago, IL • On-site

Belay Diagnostics
See more jobs at Belay Diagnosticsexternal

$80K/yr

Full-time

Re-posted 9 days ago

Key responsibilities

  • Perform sample accessioning, processing, and data generation for the laboratory.

  • Maintain documentation, review and write SOPs, and use sample tracking systems in accordance with standard operating procedures.

  • Perform quality control of samples and data, and maintain laboratory equipment and instrumentation.

Job description

PURPOSE:
Must be authorized to work in the United States. With minimal oversight from the Manager/Supervisor of the Laboratory, the Molecular Technologist will be responsible for processing both clinical and research samples using cutting-edge technologies for nucleic acid analysis, including but not limited to next-generation sequencing, Sanger sequencing, qPCR and associated sample preparation technologies. These activities are performed under CLIA/CAP regulations and will directly impact human health and thus must meet the highest possible standards for quality and integrity. Technologist roles are distinguishable primarily by level of experience, supervision required, proficiency in problem solving, certification and wider range of training.
Different schedules available.
Must have experience performing NGS assays in a high complexity clinical laboratory.
KEY RESPONSIBILITIES:
This role is responsible for the efficient and quality execution of sample accessioning, processing and data generation for the Laboratory. This includes working with the manager to maintain all documentation required for operation under CLIA/CAP certification, including review and writing of SOPs as necessary and use of sample tracking systems in accordance with standard operating procedures.
  • Timely completion of training assigned by management or laboratory director to meet the needs of laboratory operations
  • Ensure sample accessioning is performed in an accurate manner to enable effective testing of samples downstream as ordered.
  • Work with pathologist to evaluated neoplastic content of sample as needed
  • Sample processing including nucleic acid purification and preparation for sequencing and PCR is performed per established processes
  • Accurate and timely maintenance of operational metrics
  • Maintains and updates associated process documentation, participates in continuous process improvements and ongoing training
  • Performs quality control of samples processed and data generated prior to sending to next steps.
  • Maintenance of auxiliary and capital equipment and instrumentation

This role is also responsible for the development and validation of new methodologies, including establishing novel workflows, evaluating new instrumentation and protocols as deemed necessary by the clinical laboratory manager and/or director
  • Makes technological/scientific contributions to development projects
  • Research, evaluate, and implement new and emerging applications and tools to improve current clinical offerings and to support new clinical offerings. This will involve working closely and coordinating with regulatory, computational sciences, IT, and management groups in accordance with established professional development goals

MINIMUM QUALIFICATIONS:
  • Education and Experience Requirements - Bachelor's and/or Master's degree in biological or chemical sciences with experience in a regulated laboratory environment (CLIA/CAP), and ASCP Certification in Molecular Biology
  • Well organized, with strong attention to detail and process is required
  • Ability to learn new tasks and procedures in appropriate timeframes
  • Experience in data management, including laboratory information management systems
  • Excellent written and verbal skills as would be required to communicate scientific details and respond to custom inquiries

Apply