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Biotech Contract Manager Jobs in Oregon (NOW HIRING)

Senior Process Engineer

Bend, OR · On-site

$109K - $141K/yr

Hi, My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions ... Bend, OR Duration: 12+ Month Contract Position Overview We are seeking an experienced Senior ...

Securing all required contracts, paperwork and documentation as well as payments and fees as needed ... or biotech. * Strong work ethic and time management skills * Ability to make effective and ...

Securing all required contracts, paperwork and documentation as well as payments and fees as needed ... or biotech. * Strong work ethic and time management skills * Ability to make effective and ...

Securing all required contracts, paperwork and documentation as well as payments and fees as needed ... or biotech. * Strong work ethic and time management skills * Ability to make effective and ...

Securing all required contracts, paperwork and documentation as well as payments and fees as needed ... or biotech. * Strong work ethic and time management skills * Ability to make effective and ...

Manufacturing Operator I

Eugene, OR · On-site

$16 - $18/hr

Overview TekWissen Group is a workforce management provider throughout the USA and many other countries worldwide. The job opportunity below is for one of our clients specializing in biotechnology ...

Manufacturing Operator I

Eugene, OR · On-site

$16 - $18/hr

Overview TekWissen Group is a workforce management provider throughout the USA and many other countries worldwide. The job opportunity below is for one of our clients specializing in biotechnology ...

Manufacturing Operator I

Eugene, OR · On-site

$16 - $18/hr

Overview TekWissen Group is a workforce management provider throughout the USA and many other countries worldwide. The job opportunity below is for one of our clients specializing in biotechnology ...

Formulation Technician II

Bend, OR · On-site

$25 - $27/hr

TekWissen Group is a workforce management provider throughout the USA and many other countries ... The job opportunity is for one of our clients specializing in biotechnology product development ...

Showing results 21-40

Biotech Contract Manager information

What is a biotech contract manager?

A Biotech Contract Manager oversees contracts related to biotechnology partnerships, vendors, research agreements, and regulatory compliance. They negotiate terms, ensure adherence to legal and industry standards, and mitigate risks for their organization. Their role requires collaboration with legal teams, procurement, and scientific departments to support business objectives. Effective contract management helps biotech companies streamline operations, maintain compliance, and optimize financial and operational outcomes.

What are the typical day-to-day responsibilities of a biotech contract manager?

As a Biotech Contract Manager, your daily tasks often include drafting, reviewing, and negotiating a variety of contracts such as research agreements, vendor contracts, and licensing deals. You will regularly collaborate with legal, procurement, research, and finance teams to ensure terms align with company goals and regulatory requirements. Managing timelines, tracking key deliverables, and monitoring compliance throughout the contract lifecycle are also core parts of the role. This position requires balancing multiple priorities and maintaining strong communication with both internal teams and external partners to support the company’s scientific and commercial objectives.

What are the key skills and qualifications needed to thrive as a biotech contract manager?

A Biotech Contract Manager should possess a strong background in contract law, negotiation, and life sciences, often supported by a bachelor's or master's degree in a related field and relevant experience in biotech or pharmaceutical contract management. Familiarity with contract management software, compliance platforms (such as Icertis or DocuSign), and regulatory guidelines like FDA and GxP is highly beneficial. Superior attention to detail, analytical thinking, and excellent interpersonal and communication skills set outstanding professionals apart in this role. These capabilities ensure accurate and efficient contract execution, risk mitigation, and effective collaboration with internal and external stakeholders in a highly regulated industry.

What are popular job titles related to Biotech Contract Manager jobs in Oregon?

For Biotech Contract Manager jobs in Oregon, the most frequently searched job titles are:

Infographic showing various Biotech Contract Manager job openings in Oregon as of July 2026, with employment types broken down into 88% Full Time, 4% Part Time, 1% Temporary, 6% Contract, and 1% Nights. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution.

Senior Process Engineer

Stark Pharma Solutions Inc

Bend, OR • On-site

$109K - $141K/yr

Contractor

Re-posted 13 days ago


Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Senior Process Engineer

Location: Bend, OR

Duration: 12+ Month Contract

Position Overview

We are seeking an experienced Senior Process Engineer to support pharmaceutical and API manufacturing projects from design through commissioning and qualification. This role will provide technical leadership for process engineering activities, equipment design reviews, vendor management, and facility implementation within a GMP-regulated environment.

The ideal candidate will have extensive experience in pharmaceutical process design, OSD manufacturing, cleanroom facilities, and project execution across the full project lifecycle.

Key Responsibilities

  • Lead process engineering activities for pharmaceutical and API manufacturing projects.
  • Review, redline, and approve engineering design packages, including:
  • P&IDs
  • Equipment Specifications
  • Data Sheets
  • Equipment Calculations
  • Technical Drawings
  • Provide oversight and technical direction to OEM equipment vendors throughout project execution.
  • Ensure facility and process designs comply with GMP requirements and cleanroom design standards.
  • Support process equipment selection, installation, startup, commissioning, qualification, and validation activities.
  • Participate in HAZOPs, risk assessments, and process safety reviews.
  • Collaborate with Engineering, Manufacturing, Quality, Validation, and external vendors to ensure successful project delivery.
  • Verify compliance with Occupational Exposure Limits (OEL) and Occupational Exposure Bands (OEB) throughout facility and process design.
  • Support troubleshooting, optimization, and continuous improvement initiatives for manufacturing processes.
  • Contribute to project planning, execution, and technical decision-making across multiple workstreams.

Required Qualifications

  • Bachelor's degree in Chemical Engineering, Mechanical Engineering, Pharmaceutical Engineering, or a related technical discipline.
  • 10+ years of process engineering experience within pharmaceutical, API, biotechnology, or life sciences manufacturing environments.
  • Strong experience reviewing and approving process engineering design documentation.
  • Hands-on experience with:
  • Oral Solid Dosage (OSD) Manufacturing
  • Powder Handling Systems
  • CIP (Clean-in-Place) Systems
  • SIP (Sterilize-in-Place) Systems
  • Thorough understanding of GMP facility design and ISO cleanroom requirements.
  • Experience managing OEM equipment suppliers and external engineering partners.
  • Experience leading projects through design, construction, commissioning, qualification, and validation phases.
  • Strong knowledge of process safety, risk assessments, and HAZOP methodologies.