Associate Director, Finished Product and Supply Chain Operations

Reposted 14 Days Ago
Be an Early Applicant
Redwood City, CA, USA
In-Office
170K-200K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
The Associate Director oversees supply chain and manufacturing operations, ensuring compliance under cGMP standards and managing production processes with CMOs.
Summary Generated by Built In
Title:                          Associate Director, Finished Product and Supply Chain Operations
Reports to:            Director, Drug and Finished Product Manufacturing
Location:                Redwood City, California
Classification:    Exempt
 

Overview:

The Associate Director of Finished Product and Supply Chain Operations support commercial and pre‑commercial packaging component development, technology transfer, and labeling/artwork processes in addition to supply chain and inventory management with Coherus’ supply operations.  This role works closely with Contract Manufacturing Organizations (CMOs), internal cross‑functional teams, and external suppliers to ensure compliant, efficient, and high‑quality manufacturing, labeling, packaging, and supply logistics operations under cGMP standards.  The position is also responsible for special projects, SWAT team operations, and risk mitigation to address contract manufacturing operations matters as needed.

Responsibilities:

Finished Product / Combination Product Process Development

  • Lead technology transfers for finished product manufacturing.
  • Ensure CMO execution aligns with development procedures and best practices.
  • Design and execute process characterization studies.
  • Support product serialization requirements across global markets.
  • Author CMC sections of regulatory submissions and act as technical contact during agency interactions.

Assembly, Labeling & Packaging Operations

  • Serve as technical lead for CMO operations related to assembly, labeling, and packaging.
  • Support deviations, CAPAs, change controls, process monitoring, and process improvement initiatives.
  • Represent the company as person‑in‑plant during manufacturing and packaging operations.

Labeling / Artwork Management

  • Oversee development, review, and approval of clinical and commercial labeling with internal and external partners.
  • Ensure compliance with regulatory and SOP requirements in labeling content.
  • Support development and improvement of tools and processes for label content, graphics, translation, and proofreading workflows.

Quality & Compliance

  • Ensure adherence to cGMP, ICH, EMA, FDA, OSHA, and internal corporate quality standards.
  • Ensure compliance with device/combination product design control and labeling requirements.
  • Support audits, inspections, and quality initiatives across supply chain and finished product operations.
  • Travel domestically and internationally up to 25% as required.

Commercial & Pre‑Commercial Supply Chain Management

  • Generate production and storage purchase orders for CMO sites per the master production schedule.
  • Coordinate daily shipments of bulk drug substance, drug product, and finished goods.
  • Track commercial and pre‑commercial sample shipments and proactively resolve logistics issues.
  • Maintain master production schedule data, including part numbers, lot numbers, CMO locations, and quantities.
  • Execute daily inventory transactions: stock transfers, work orders, adjustments, disposals.
  • Manage drug returns for redistribution or disposal.
  • Review inventory reports for quantity, expiration, and lot status; rebalance inventories across CMOs.
  • Investigate and resolve inventory discrepancies.
  • Escalate raw material shortages that may impact supply continuity.
  • Coordinate domestic and international shipments per company SOPs and compliance requirements.
  • Support logistics‑related studies, SOP development, and shipping validations for product launches.

Qualifications:

Required Education & Experience

  • BS in packaging engineering, mechanical engineering, or related field preferred.
  • Minimum 7+ years’ final product, supply chain and manufacturing ops leadership experience in biopharmaceuticals.

Preferred Qualifications

  • Strong knowledge of transportation/logistics and import/export compliance.
  • Experience working within compliant import/export programs (pharma/biopharma/chemical).

The Base Salary Range for this position is $170,000 to $200,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.

Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.

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The Company
Redwood City, California
323 Employees
Year Founded: 2010

What We Do

Coherus is a commercial-stage biopharmaceutical company focused on the research, development, and commercialization of innovative immunotherapies to treat cancer and the commercialization of our portfolio of FDA-approved therapeutics. We are building a leading oncology company backed by in-house expertise and an established infrastructure from our diversified portfolio of FDA-approved biosimilar products. If you are interested in joining a highly innovative and exciting company, please visit our careers webpage at http://www.coherus.com/careers/ for a list of career opportunities

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