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Biotech Manufacturing Jobs in Oregon (NOW HIRING)

Stark Pharma Solutions Inc

Senior Process Engineer

Bend, OR · On-site

$109K - $141K/yr

... biotechnology, or life sciences manufacturing environments. * Strong experience reviewing and approving process engineering design documentation. * Hands-on experience with: * Oral Solid Dosage (OSD ...

Re:Build Manufacturing

OR

... manufacturing. Our customers span a wide array of industries including aerospace, defense, mobility, healthcare, pharma, biotech, clean tech, chemicals, energy, lifestyle, food production, and ...

Genentech

Principal Project Scheduler

Hillsboro, OR

$119K - $222K/yr

... manufacturing excellence and innovation. As Lead Scheduler, you will be the scheduling expert and strategic partner for complex biotech projects, collaborating closely with cross-functional teams ...

Astrix Inc

Quality Inspector

Clackamas, OR · On-site

Quality experience in food, nutraceutical, manufacturing, biotech, or pharma * Experience with FDA/cGMP compliance * Hands-on experience with non-conformances, OOS investigations, and documentation

Telix Pharmaceuticals (AMER)

OR · On-site

... manufacturing/supply chain, and commercial, and drives governance, decision-making, and risk ... Master's or PhD in medical, pharma or biotech field strongly preferred; 12+ years in pharma/biotech ...

TekWissen LLC

IT Infrastructure Project Manager

Bend, OR · On-site

$50 - $65/hr

Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new ...

Axiom Talent Platform

Pharmaceutical Contracts Lawyers

OR · On-site +1

$309K/yr

... or biotech organizations. Responsibilities: * Draft, review, and negotiate a high volume of ... Support manufacturing and supply chain-related agreements, including those involving CMOs, CDMOs ...

Axiom Talent Platform

Pharmaceutical Contracts Lawyers

OR · On-site +1

$309K/yr

... or biotech organizations. Responsibilities: * Draft, review, and negotiate a high volume of ... Support manufacturing and supply chain-related agreements, including those involving CMOs, CDMOs ...

Telix Pharmaceuticals (AMER)

OR · On-site

... biotechnology industry by leading/influencing high-performing teams. With a deep understanding of ... Good Manufacturing Practices (GMP) * Demonstrate familiarity and compliance with ICH and GMP ...

TekWissen LLC

Documentation Specialist

Bend, OR · On-site

$19 - $24/hr

Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new ...

Astrix Inc

Quality Inspector I

Clackamas, OR · On-site

$22 - $23/hr

Prior manufacturing or laboratory environment experience. Familiarity with FDA/cGMP standards preferred. MUST have Nutraceutical, food & beverage, biotech, pharma (GMP regulated industry working with ...

TekWissen LLC

Formulation Technician II

Bend, OR · On-site

$25 - $27/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... Performs current Good Manufacturing Practices (cGMP) production of pharmaceutical Spray Dried ...

Lonza

Instrumentation Specialist

Bend, OR · On-site

... to manufacture medicines to the highest quality and safety standards. Today, Lonza is a global ... Lonza Pharma & Biotech has an opening for an Instrumentation Specialist at our Bend, OR site. In ...

Lonza

Instrumentation Specialist

Bend, OR · On-site

... to manufacture medicines to the highest quality and safety standards. Today, Lonza is a global ... Lonza Pharma & Biotech has an opening for an Instrumentation Specialist at our Bend, OR site. In ...

Lonza

Instrumentation Specialist

Bend, OR · On-site

... to manufacture medicines to the highest quality and safety standards. Today, Lonza is a global ... Lonza Pharma & Biotech has an opening for an Instrumentation Specialist at our Bend, OR site. In ...

Lonza

Instrumentation Specialist

Portland, OR · On-site

... to manufacture medicines to the highest quality and safety standards. Today, Lonza is a global ... Lonza Pharma & Biotech has an opening for an Instrumentation Specialist at our Bend, OR site. In ...

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All JobsBiotech Manufacturing JobsBiotech Manufacturing Jobs in Oregon

Biotech Manufacturing information

See Oregon salary details

$12

$22

$35

How much do biotech manufacturing jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biotech manufacturing in Oregon is $22.03, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $24.66 per hour, depending on experience, location, and employer.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

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

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

How to get into biotech manufacturing?

To enter biotech manufacturing, candidates typically need a background in biology, chemistry, or related fields, often requiring a bachelor's degree or higher. Gaining experience through internships or entry-level positions, developing skills in laboratory techniques and GMP (Good Manufacturing Practice), and obtaining certifications such as cGMP training can improve job prospects. Familiarity with manufacturing equipment and attention to quality control are also important for success in this field.
What are popular job titles related to Biotech Manufacturing jobs in Oregon? For Biotech Manufacturing jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Biotech Manufacturing jobs in Oregon look for? The top searched job categories for Biotech Manufacturing jobs in Oregon are:
What cities in Oregon are hiring for Biotech Manufacturing jobs? Cities in Oregon with the most Biotech Manufacturing job openings:
Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in Oregon as of August 2026, with employment types broken down into 75% Full Time, 19% Part Time, 1% Temporary, 3% Contract, and 2% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $45,824 per year, or $22 per hour.

Senior Process Engineer

Stark Pharma Solutions Inc

Bend, OR • On-site

$109K - $141K/yr

Contractor

Re-posted yesterday

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.