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Contract Manufacturing Jobs in Tennessee (NOW HIRING)

Medtronic

Sr. Manufacturing Engineer

Memphis, TN

$88K - $120K/yr

The facility provides comprehensive services in product release for contract manufactured products, product packaging, surgical kitting, device software loading, and custom spinal rod manufacturing.

New

Medtronic

Sr. Manufacturing Engineer

Memphis, TN · On-site

$88K - $120K/yr

The facility provides comprehensive services in product release for contract manufactured products, product packaging, surgical kitting, device software loading, and custom spinal rod manufacturing.

New

Medtronic

Sr. Manufacturing Engineer

Memphis, TN · On-site

$88K - $120K/yr

The facility provides comprehensive services in product release for contract manufactured products, product packaging, surgical kitting, device software loading, and custom spinal rod manufacturing.

New

Vijon, Inc.

VP AND GENERAL MANAGER

Smyrna, TN · On-site

Develop and maintain a network of cost-effective contract manufacturing partners capable of supporting manufacturing requirements of the branded business * Work closely with the supply chain to ...

Vi-Jon

VP AND GENERAL MANAGER

Smyrna, TN

Develop and maintain a network of cost-effective contract manufacturing partners capable of supporting manufacturing requirements of the branded business * Work closely with the supply chain to ...

Laborup

Technical Program Manager

Nashville, TN · On-site

$90K - $110K/yr

Overview We're hiring a Technical Program Manager for our aerospace and defense contract manufacturing company. We're a low-volume manufacturer building complex machined, welded, and fabricated ...

Laborup

Technical Program Manager

Nashville, TN · On-site

$90K - $110K/yr

Overview We're hiring a Technical Program Manager for our aerospace and defense contract manufacturing company. We're a low-volume manufacturer building complex machined, welded, and fabricated ...

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Showing results 1-20

All JobsContract Manufacturing JobsContract Manufacturing Jobs in Tennessee

Contract Manufacturing information

See Tennessee salary details

$27.7K

$88.5K

$139.3K

How much do contract manufacturing jobs pay per year?

As of Aug 7, 2026, the average yearly pay for contract manufacturing in Tennessee is $88,543.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,800.00 and $109,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in contract manufacturing?

Excelling in contract manufacturing requires a solid understanding of production processes, supply chain management, and quality control, often backed by a degree in engineering, manufacturing, or business. Familiarity with ERP systems, manufacturing execution systems (MES), and ISO or GMP certifications is highly valued. Strong negotiation skills, attention to detail, and effective communication are essential soft skills. These competencies help ensure efficient production, seamless client collaboration, and adherence to quality and regulatory standards.

What does a contract manufacturing do?

A contract manufacturing professional oversees the production of goods on behalf of a client company, ensuring products meet quality standards and specifications. They coordinate with suppliers, manage manufacturing processes, and often work with tools like ERP systems to streamline operations.

What is contract manufacturing?

A Contract Manufacturing job involves managing the production of goods through third-party manufacturers. Professionals in this role oversee vendor relationships, ensure quality control, negotiate contracts, and coordinate supply chain logistics. They work closely with suppliers to meet cost, production, and timeline requirements. This position is common in industries like pharmaceuticals, electronics, and consumer goods.

What types of companies or industries typically hire for contract manufacturing roles?

Contract manufacturing roles are in demand across a wide variety of industries, including pharmaceuticals, consumer goods, electronics, automotive, and food and beverage. Job seekers can expect to find opportunities with both specialized contract manufacturing organizations (CMOs) and large corporations that outsource aspects of their production processes. These positions often involve collaborating with diverse clients, managing production timelines, and ensuring adherence to high quality and regulatory standards. Working in this field can provide valuable exposure to multiple industries, offering strong potential for career advancement and skill development.

What are the most commonly searched types of Manufacturing jobs in Tennessee? The most popular types of Manufacturing jobs in Tennessee are:
What are popular job titles related to Contract Manufacturing jobs in Tennessee? For Contract Manufacturing jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Contract Manufacturing jobs in Tennessee look for? The top searched job categories for Contract Manufacturing jobs in Tennessee are:
What cities in Tennessee are hiring for Contract Manufacturing jobs? Cities in Tennessee with the most Contract Manufacturing job openings:
Contract Manufacturing jobs near you
Infographic showing various Contract Manufacturing job openings in Tennessee as of August 2026, with employment types broken down into 84% Full Time, 3% Temporary, 10% Contract, and 3% Nights. Highlights an 100% In-person job distribution, with an average salary of $88,543 per year, or $42.6 per hour.

Staff Product Transfer Project Engineer - Bioprocessing

WilsonCTS

Franklin, TN • Hybrid

$60 - $64/hr

Other

Posted 6 days ago

Job description

Job Title: Staff Product Transfer Project Engineer - Bioprocessing
Employment Type: Contract (18-months)
Work Location: Franklin, Tennessee
Work Arrangement: Hybrid (3 days - onsite)
Pay Rate: $60-$64 per hour
Travel: Up to 25% domestic and international travel, depending on project phase

Position Summary

We are seeking an experienced Staff Product Transfer Project Engineer - Bioprocessing to provide technical leadership for complex biologics manufacturing technology transfer programs between Contract Manufacturing Organizations and internal manufacturing sites.

This role will support sterile injectable biologic drug products and will lead engineering activities across process development, technology transfer, scale-up, qualification, validation, regulatory support, and commercial manufacturing readiness.

The successful candidate will serve as a key technical and engineering liaison between external manufacturing partners and internal Technical Operations, Regulatory Affairs, Quality, Manufacturing, Supply Chain, Validation, and cross-functional project teams. This position is well suited for someone with strong biologics manufacturing knowledge, cGMP experience, technical project leadership, and experience supporting technology transfers in FDA-regulated environments.

Key Responsibilities

Technology Transfer and Engineering Leadership
  • Lead end-to-end bioprocess technology transfer activities between external manufacturing partners and internal manufacturing sites.
  • Support process adaptation, scale-up, equipment qualification, validation, and commercial readiness activities.
  • Provide technical leadership for sterile injectable biologic drug product transfer programs.
  • Partner with internal and external teams to ensure transfer activities are executed in alignment with technical, quality, regulatory, and project requirements.
  • Identify technical risks, project dependencies, process gaps, and execution challenges throughout the transfer lifecycle.
  • Support successful transition of products and processes into commercial manufacturing.
Cross-Functional and CMO Partnership
  • Serve as the primary engineering liaison between Contract Manufacturing Organizations and internal teams.
  • Collaborate with Technical Operations, Regulatory Affairs, Quality, Manufacturing, Supply Chain, Validation, and external partners.
  • Lead technical discussions with internal teams and external manufacturing partners.
  • Communicate project status, risks, technical issues, and recommendations to leadership and stakeholders.
  • Drive issue resolution and ensure alignment across functions during transfer, qualification, validation, and manufacturing readiness activities.
  • Build strong working relationships with CMOs and internal stakeholders to support timely project execution.
Risk Assessment and Technical Problem Solving
  • Conduct engineering gap assessments to identify technical, process, equipment, validation, or documentation risks.
  • Perform technical risk evaluations using structured methodologies such as FMEA.
  • Support root-cause analysis and technical investigations related to process transfer, qualification, validation, or manufacturing readiness challenges.
  • Develop recommendations to address technical gaps and reduce transfer risk.
  • Ensure engineering decisions are supported by sound technical rationale, data, and regulatory expectations.
Validation, Qualification, and Manufacturing Readiness
  • Support IQ, OQ, PQ, GMP, non-GMP, engineering, and PPQ campaign execution.
  • Review protocols, reports, batch records, validation documentation, technical records, and transfer documentation.
  • Ensure documentation aligns with regulatory expectations, quality standards, project timelines, and internal procedures.
  • Support analytical test method transfer activities as needed.
  • Partner with validation, quality, manufacturing, and technical teams to confirm readiness for process execution and commercial production.
  • Provide technical support during manufacturing campaigns, process qualification, and post-transfer activities.
Regulatory and Compliance Support
  • Support regulatory submissions and technical documentation related to manufacturing transfers.
  • Provide technical input for Biologics License Application supplements, inspection readiness, and regulatory justifications.
  • Support documentation and technical rationale for post-approval manufacturing changes.
  • Ensure transfer and engineering activities comply with FDA, EMA, ICH, cGMP, and applicable regulatory expectations.
  • Support inspection readiness through documentation review, technical explanations, and cross-functional preparation.
Change Control and Documentation
  • Manage engineering change strategies, ECOs, and documentation release activities through change control systems.
  • Support change control planning and execution for process, equipment, documentation, analytical method, and manufacturing transfer changes.
  • Prepare, review, and maintain technical documentation, risk assessments, reports, protocols, and project records.
  • Ensure documentation is accurate, complete, traceable, and aligned with quality and regulatory requirements.
  • Perform additional duties as assigned to support Product Transfer and Technical Operations.
Required Qualifications
  • Master's degree or Ph.D. preferred in Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, Engineering, or a related scientific or technical discipline.
  • Bachelor's degree may be considered with significant relevant experience.
  • Minimum of 4 years of engineering experience in biotechnology, biologics, pharmaceutical, medical device, or other highly regulated industries.
  • Minimum of 4 years of experience supporting technology transfer, manufacturing engineering, process engineering, validation, or scale-up in FDA-regulated cGMP environments.
  • Experience supporting biologics manufacturing, bioprocessing, sterile manufacturing, or injectable drug product operations.
  • Strong technical writing, documentation, and communication skills.
  • Strong project management, organizational, and stakeholder-influence skills.
  • Ability to work effectively in highly regulated environments.
  • Ability to travel domestically and internationally up to 25%, depending on project needs.
  • Ability to work in a hybrid role based in Franklin, Tennessee.
Preferred Qualifications
  • Experience working with Contract Manufacturing Organizations.
  • Scientific leadership experience in GMP biologics manufacturing.
  • Experience with sterile injectable biologic drug products.
  • Experience supporting BLA supplements, regulatory submissions, inspection readiness, or post-approval manufacturing changes.
  • Experience with upstream and downstream bioprocessing.
  • Experience with single-use systems, protein formulation, stability, and analytical methods.
  • Experience supporting analytical test method transfers.
  • Experience reviewing or executing IQ, OQ, PQ, PPQ, engineering runs, GMP, and non-GMP campaign documentation.
  • Experience with ECOs, change control systems, documentation release, and technical transfer governance.
  • Experience using FMEA or similar structured risk assessment tools.

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