Serán BioScience logo
Biotechnology, Pharmaceutical, Contract Research Organization (CRO)

Manufacturing Production Planner

Bend, OROnsiteFull TimePosted 18 days ago

Is this role right for you?

Upload your resume and get a skill-by-skill breakdown — see exactly where you match, where you're close, and what to highlight. Not a mystery percentage.

Get a tailored resume highlighting what this role needs.

Required skills

  • Manufacturing Production Planner
  • production schedule
  • GMP manufacturing
  • material availability
  • equipment readiness
  • client deliverables
  • clinical timelines
  • development timelines
  • Manufacturing
  • Supply Chain

Nice to have

  • SAP
  • Oracle
  • NetSuite
  • Microsoft Dynamics

Role summary

Serán is seeking a Manufacturing Production Planner to develop, maintain, and optimize production schedules for GMP manufacturing. This role requires coordinating cross-functional activities, ensuring alignment between manufacturing campaigns, material availability, equipment readiness, quality requirements, and client deliverables to support clinical and development timelines. The planner will act as a liaison between various departments, including Manufacturing, Supply Chain, Quality Assurance, and Project Management, to ensure efficient production operations and compliance with GMP regulations. Key responsibilities include determining resource needs, addressing issues, participating in risk assessments, and facilitating scheduling meetings. A strong understanding of manufacturing planning principles and experience with ERP/MRP systems are preferred.

Serán is seeking a Manufacturing Production Planner who will be responsible for developing, maintaining, and optimizing the production schedule for GMP manufacturing activities. This role coordinates cross-functional activities to ensure manufacturing campaigns, material availability, equipment readiness, quality requirements, and client deliverables are aligned to support clinical and development timelines. 

This position serves as a key liaison between Manufacturing, Supply Chain, Quality Assurance, Project Management, Product and Process Development, Facilities, Quality Control, and Business Development to ensure efficient execution of production operations while maintaining compliance with applicable GMP regulations and internal quality standards. 


The Manufacturing Production Planner works closely with department directors to:

  • Determine manpower, equipment and raw materials needed to cover production demand.
  • Address issues when they arise aiming for minimum disruption.
  • Assist in production risk assessment and mitigation activities.
  • Participate in conflict resolution with stakeholders. 

Duties & Responsibilities

  • Develop and maintain detailed short-term and long-term production schedules for GMP and non-GMP manufacturing activities.
  • Establish manufacturing priorities based on business objectives, client commitments, material availability and resource constraints.
  • Monitor schedule adherence and communicate schedule changes, delays, risks, and recovery plans to stakeholders.
  • Facilitate weekly and daily scheduling meetings and communicate updates to cross-functional teams.
  • Develop and maintain manufacturing capacity models, identify bottlenecks and provide recommendations to improve throughput, utilization, and monthly production planning processes.
  • Evaluate facility, equipment, labor, and material constraints impacting production schedules.
  • Maintain accurate planning data within ERP, MES, MRP, or scheduling systems.
  • Required Skills & Abilities

  • Excellent verbal and written communication skills.
  • Strong understanding of manufacturing planning and scheduling principles.
  • Ability to manage multiple projects and rapidly changing priorities.
  • Experience with ERP/MRP systems such as SAP, Oracle, NetSuite, Microsoft Dynamics, or similar platforms preferred.
  • Excellent interpersonal and customer service skills.
  • Excellent organizational skills and attention to detail.
  • Excellent time management skills with a proven ability to meet deadlines.
  • Strong analytical and problem-solving skills.
  • Ability to function well in a high-paced and at times stressful environment.
  • Proficient with Microsoft Office Suite or related software.
  • Education & Experience

    High school diploma or equivalent, and 3 years of production scheduling, planning, manufacturing operations, or supply chain experience, preferably in a GMP environment; or an equivalent combination of education and experience. CDMO, clinical manufacturing, or early-phase development experience highly desirable.

    Physical Requirements

  • Prolonged periods of sitting or standing at a desk and working on a computer
  • Must be able to lift up to 25 pounds regularly
  • Adheres to consistent and predictable in-person attendance
  • Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon. Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Benefits Summary: Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance. The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    Ready to apply?
    You'll be redirected to Serán BioScience's application page.

    Similar roles

    See how RiseMe works

    Match, tailor, and prep so you send fewer applications and land more interviews.