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Production Control Manager Jobs in Culver, OR (NOW HIRING)

... control. Manages operations within the budget. Provides productivity oversight and review. Works ... with leadership to achieve productivity standards. Develops and implements annual plan including ...

Work with the Receiving Manager and the Inventory Controller to plan and execute proper ordering, par level setting, and inventory procedures to ensure proper product control. Help the Inventory ...

Work with the Receiving Manager and the Inventory Controller to plan and execute proper ordering, par level setting, and inventory procedures to ensure proper product control. Help the Inventory ...

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Kitchen Manager/Sous Chef

Bend, OR · On-site

$55K - $63K/yr

Job Summary Looking for a motivated, organized and skilled sous chef/kitchen manager to join our ... · Control food cost and usage by following proper requisition of products from storage areas ...

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Kitchen Manager/Sous Chef

Bend, OR · On-site

$55K - $63K/yr

Job Summary Looking for a motivated, organized and skilled sous chef/kitchen manager to join our ... · Control food cost and usage by following proper requisition of products from storage areas ...

Showing results 21-40

Production Control Manager information

See Culver, OR salary details

$32K

$88.8K

$142.8K

How much do production control manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for production control manager in Culver, OR is $88,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,400.00 and $105,700.00 per year, depending on experience, location, and employer.

What is a production control manager?

A Production Control Manager is responsible for overseeing and coordinating the scheduling, planning, and flow of production activities within a manufacturing facility. They ensure that production targets are met efficiently, materials and resources are properly allocated, and any potential delays or issues are addressed quickly. This role often involves working closely with other departments such as purchasing, inventory, and quality control to optimize production processes. Their goal is to maintain smooth operations and meet delivery deadlines while minimizing costs and waste.

What does a production control manager do?

A production control manager oversees day-to-day production activities and works to boost sales, efficiency, and labor productivity. As a production control manager, your duties involve managing production staff, coordinating machine repairs and maintenance, ensuring the project budget is met, and developing safety programs. Positions are most common with manufacturing and supply chain companies. A career as a production control manager typically requires at least an associate degree in engineering, business administration, or a related field, along with extensive experience in a factory setting. Some employers prefer a bachelor’s degree and prior management experience. Additional qualifications include strong interpersonal and managerial skills, as well as knowledge of the industry.

What are the key skills and qualifications needed to thrive as a production control manager, and why are they important?

To thrive as a Production Control Manager, you need expertise in production planning, inventory management, and supply chain logistics, usually supported by a bachelor’s degree in business, engineering, or a related field. Familiarity with ERP/MRP systems, Lean manufacturing tools, and production scheduling software is typically required. Strong analytical, leadership, and communication skills enable effective coordination across departments and quick problem-solving. These skills ensure efficient workflow, cost control, and timely delivery in fast-paced manufacturing environments.

How does a production control manager typically collaborate with other departments to ensure smooth workflow?

A Production Control Manager works closely with various departments such as procurement, manufacturing, logistics, and quality assurance to coordinate production schedules and resolve bottlenecks. They regularly communicate with team leads and supervisors to monitor progress, adjust plans in response to unforeseen challenges, and ensure that materials and resources are available when needed. This collaborative approach helps maintain efficient operations, minimize downtime, and meet delivery deadlines. Effective cross-department communication is key to success in this role.

What cities near Culver, OR are hiring for Production Control Manager jobs?

Cities near Culver, OR with the most Production Control Manager job openings:

Infographic showing various Production Control Manager job openings in Culver, OR as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $88,754 per year, or $42.7 per hour.

QC Scientist - Compendial & Analytical Quality

Lonza

Bend, OR • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago


Key responsibilities

  • Review and update internal documentation based on compendial changes to ensure compliance with pharmacopeial standards.

  • Coordinate all testing activities performed at external contract laboratories and review outsourced analytical data for regulatory compliance.

  • Evaluate and authorize analytical raw data, laboratory notebooks, and test reports to maintain data integrity and compliance.


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical


Job description

QC Scientist - Compendial & Analytical Quality
Bend, OR
The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
Lonza is looking for a QC Scientist - Compendial & Analytical Quality to join our Quality team in beautiful Bend, Oregon. This role will be responsible for reviewing and updating internal documentation based on compendial changes and ensuring QC is in compliance with official pharmacopeial monographs. Additionally, this role will be responsible for coordinating all testing activities performed at external contract laboratories and ensuring that all outsourced analytical data meets strict regulatory standards and Lonza quality requirements.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
  • Work in a safe, high-quality cGMP laboratory that values your personal growth and new ideas .
  • Day-One Insurance: Life, disability, and comprehensive health, dental, and vision insurance options.
  • 401k Match: 100% match up to 6% of your salary, plus an extra automatic company contribution.
  • Lonza bonus program: Performance-linked variable pay plan that rewards yearly company and individual success

What you will do:
  • Data & Report Authorization:Evaluate and authorize analytical raw data, laboratory notebooks, and comprehensive test reports to ensure data integrity and compliance.
  • Compendial Monitoring: Monitor and implement compendial updates to maintain strict alignment with evolving regulatory standards and pharmacopeial requirements.
  • Document Lifecycle Management: Oversee the end-to-end lifecycle of controlled documents, records, and material specifications.
  • Technical Authoring & Review:Author, review, and approve Standard Operating Procedures (SOPs), analytical methods, and validation protocols.
  • Investigations & Root Cause Analysis: Lead and support formal laboratory investigations, deviations, and comprehensive root cause analyses.
  • External Testing Oversight: Manage the end-to-end process for external laboratory testing, serving as primary liaison for CRO project timelines and method feasibility.
  • Procurement Coordination: Coordinate procurement operations, including purchase orders for external testing services and essential laboratory consumables.

What we are looking for:
  • Bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific field.
  • 3 to 5 years of hands-on specific experience working in a regulated (cGMP/GLP) pharmaceutical or biopharmaceutical quality control laboratory.
  • Deep knowledge of global pharmacopeias (USP, EP, JP, BP) for raw materials and finished products, including verification and execution of monographs.
  • Experience coordinating testing with external contract (CMOs/external labs), shipping samples, and reviewing external data.
  • Practical skill with methods like HPLC, GC, UV-Vis, FTIR, titration, and basic wet chemistry.
  • Proficient with technical writing for Standard Operating Procedures (SOPs), protocols, and data integrity requirements.
  • Ownership of evaluating and updating internal document based on compendial changes.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US